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    <title>Gastrointestinal</title>
    <description></description>
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      <title>Microbial ecology reshapes cancer care, diagnostics and therapies</title>
      <description>Cancer researchers are increasingly turning to the microbiome to understand why some patients respond well to treatment while others face severe complications. Gut microbial communities shift during intensive therapies such as bone marrow transplantation, and those changes influence infection risk, immune recovery and long‑term survival. New advances in microbial sequencing and engineering redefine this community as a measurable clinical parameter that can be monitored, modeled, and even therapeutically reshaped to improve outcomes in oncology and other conditions.</description>
      <content:encoded>
        <![CDATA[Cancer researchers are increasingly turning to the microbiome to understand why some patients respond well to treatment while others face severe complications. Gut microbial communities shift during intensive therapies such as bone marrow transplantation, and those changes influence infection risk, immune recovery and long‑term survival. New advances in microbial sequencing and engineering redefine this community as a measurable clinical parameter that can be monitored, modeled, and even therapeutically reshaped to improve outcomes in oncology and other conditions.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732621</guid>
      <pubDate>Fri, 10 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732621-microbial-ecology-reshapes-cancer-care-diagnostics-and-therapies</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Gut-Microbiome-Dysbiosis.webp?t=1783522730" type="image/jpeg" medium="image" fileSize="516866">
        <media:title type="plain">Illustration of bacteria, microorganisms in the gastrointestinal system</media:title>
      </media:content>
    </item>
    <item>
      <title>U&amp;S Bio identifies new H+/K+-ATPase inhibitors</title>
      <description>U&amp;S Bio Co. Ltd. has divulged H+/K+-ATPase inhibitors with improved stability found to be potentially useful for the treatment of gastrointestinal disorders, cancer, Helicobacter pylori infection, sialorrhea, asthma and airways obstruction, among others.</description>
      <content:encoded>
        <![CDATA[U&S Bio Co. Ltd. has divulged H+/K+-ATPase inhibitors with improved stability found to be potentially useful for the treatment of gastrointestinal disorders, cancer, <em>Helicobacter pylori</em> infection, sialorrhea, asthma and airways obstruction, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732511</guid>
      <pubDate>Thu, 09 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732511-u-and-s-bio-identifies-new-h-k-atpase-inhibitors</link>
    </item>
    <item>
      <title>Seres’ SER-155 takes on immune checkpoint inhibitor-related enterocolitis </title>
      <description>While the emergence of immune checkpoint inhibitor (ICI) therapy in recent years has significantly improved cancer outcomes, some patients have been unable to experience the full therapeutic benefits of ICIs due to significant gastrointestinal inflammation linked to treatment. Seres Therapeutics Inc. is looking to change that with its live biotherapeutic candidate, SER-155, offering impressive findings from phase I data in ICI-related enterocolitis, or irEC.</description>
      <content:encoded>
        <![CDATA[While the emergence of immune checkpoint inhibitor (ICI) therapy in recent years has significantly improved cancer outcomes, some patients have been unable to experience the full therapeutic benefits of ICIs due to significant gastrointestinal inflammation linked to treatment. Seres Therapeutics Inc. is looking to change that with its live biotherapeutic candidate, SER-155, offering impressive findings from phase I data in ICI-related enterocolitis, or irEC.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732435</guid>
      <pubDate>Wed, 08 Jul 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732435-seres-ser-155-takes-on-immune-checkpoint-inhibitor-related-enterocolitis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Gastrointestinal-vector-framework.webp?t=1739806991" type="image/jpeg" medium="image" fileSize="232822">
        <media:title type="plain">Illustration of intestinal track</media:title>
      </media:content>
    </item>
    <item>
      <title>Microbial ecology reshapes cancer care, diagnostics and therapies</title>
      <description>Cancer researchers are increasingly turning to the microbiome to understand why some patients respond well to treatment while others face severe complications. Gut microbial communities shift during intensive therapies such as bone marrow transplantation, and those changes influence infection risk, immune recovery and long‑term survival. New advances in microbial sequencing and engineering redefine this community as a measurable clinical parameter that can be monitored, modeled, and even therapeutically reshaped to improve outcomes in oncology and other conditions.</description>
      <content:encoded>
        <![CDATA[Cancer researchers are increasingly turning to the microbiome to understand why some patients respond well to treatment while others face severe complications. Gut microbial communities shift during intensive therapies such as bone marrow transplantation, and those changes influence infection risk, immune recovery and long‑term survival. New advances in microbial sequencing and engineering redefine this community as a measurable clinical parameter that can be monitored, modeled, and even therapeutically reshaped to improve outcomes in oncology and other conditions.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732480</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732480-microbial-ecology-reshapes-cancer-care-diagnostics-and-therapies</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Gut-Microbiome-Dysbiosis.webp?t=1783522730" type="image/jpeg" medium="image" fileSize="516866">
        <media:title type="plain">Illustration of bacteria, microorganisms in the gastrointestinal system</media:title>
      </media:content>
    </item>
    <item>
      <title>With tardy Tvardi phase I win, skin in STAT3 game plus GI</title>
      <description>Tvardi Therapeutics Inc. rebounded from a phase II blowup last fall in idiopathic pulmonary fibrosis (IPF) with oral STAT3 inhibitor TTI-101 by showing that a next-gen phosphate prodrug dubbed TTI-109 kept its potency in phase I without gastrointestinal (GI) troubles.</description>
      <content:encoded>
        <![CDATA[Tvardi Therapeutics Inc. rebounded from a phase II blowup last fall in idiopathic pulmonary fibrosis (IPF) with oral STAT3 inhibitor TTI-101 by showing that a next-gen phosphate prodrug dubbed TTI-109 kept its potency in phase I without gastrointestinal (GI) troubles.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732418</guid>
      <pubDate>Tue, 07 Jul 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732418-with-tardy-tvardi-phase-i-win-skin-in-stat3-game-plus-gi</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Stock-chart-upward-arrow.webp?t=1623701362" type="image/png" medium="image" fileSize="491722">
        <media:title type="plain">Stock chart, upward arrow</media:title>
      </media:content>
    </item>
    <item>
      <title>Ribocure and Madrigal nominate siRNA drug candidate for MASH</title>
      <description>Ribocure Pharmaceuticals AB, a subsidiary of Suzhou Ribo Life Science Co. Ltd., and Madrigal Pharmaceuticals Inc. have achieved the first drug candidate nomination within their siRNA partnership.</description>
      <content:encoded>
        <![CDATA[Ribocure Pharmaceuticals AB, a subsidiary of Suzhou Ribo Life Science Co. Ltd., and Madrigal Pharmaceuticals Inc. have achieved the first drug candidate nomination within their siRNA partnership.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732357</guid>
      <pubDate>Thu, 02 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732357-ribocure-and-madrigal-nominate-sirna-drug-candidate-for-mash</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/RNA-siRNA-mRNA-nanoparticle-delivery.webp?t=1755185305" type="image/jpeg" medium="image" fileSize="699795">
        <media:title type="plain">Illustration of RNA strands being delivered by nanoparticles</media:title>
      </media:content>
    </item>
    <item>
      <title>Trex Bio discloses TRB-071 as CD30 agonist antibody</title>
      <description>Trex Bio Inc. has disclosed that its development candidate TRB-071, currently in IND-enabling studies, is a CD30 agonist antibody. The approach could have therapeutic potential in inflammatory bowel disease and other autoimmune and inflammatory diseases.</description>
      <content:encoded>
        <![CDATA[Trex Bio Inc. has disclosed that its development candidate TRB-071, currently in IND-enabling studies, is a CD30 agonist antibody. The approach could have therapeutic potential in inflammatory bowel disease and other autoimmune and inflammatory diseases.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732331</guid>
      <pubDate>Wed, 01 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732331-trex-bio-discloses-trb-071-as-cd30-agonist-antibody</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/IBD-inflammatory-bowel-disease-Crohns-Colitis.webp?t=1745258495" type="image/jpeg" medium="image" fileSize="193405">
        <media:title type="plain">Illustration of intestines with inflammation</media:title>
      </media:content>
    </item>
    <item>
      <title>Relaxed on Abivax: UC phase III cancer answer quells fretting</title>
      <description>Wall Street breathed easier, and shares of Abivax SA found relief as further phase III data from the Abtect maintenance trial were disclosed with obefazimod in ulcerative colitis (UC).</description>
      <content:encoded>
        <![CDATA[Wall Street breathed easier, and shares of Abivax SA found relief&nbsp;as further phase III data from the Abtect maintenance trial were disclosed with obefazimod in ulcerative colitis (UC).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732245</guid>
      <pubDate>Tue, 30 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732245-relaxed-on-abivax-uc-phase-iii-cancer-answer-quells-fretting</link>
    </item>
    <item>
      <title>CINP 2026: Gut microbiota could predict antidepressant response</title>
      <description>The gut microbiota may be altered in people with depression as a result of treatment. These microorganisms reorganize differently in individuals who respond to therapy. In a multiomics study of antidepressant-naive patients presented at the 2026 World Congress of Neuropsychopharmacology (CINP), scientists from National Taiwan University found that patients who improved after antidepressant treatment maintained a more balanced and functional microbial ecosystem, recovered beneficial metabolites, and displayed blood-based biological signals that aligned with these changes.</description>
      <content:encoded>
        <![CDATA[The gut microbiota may be altered in people with depression as a result of treatment. These microorganisms reorganize differently in individuals who respond to therapy. In a multiomics study of antidepressant-naive patients presented at the 2026 World Congress of Neuropsychopharmacology (CINP), scientists from National Taiwan University found that patients who improved after antidepressant treatment maintained a more balanced and functional microbial ecosystem, recovered beneficial metabolites, and displayed blood-based biological signals that aligned with these changes.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732354</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732354-cinp-2026-gut-microbiota-could-predict-antidepressant-response</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Brain-gut-axis-connection-illustration.webp?t=1782743853" type="image/jpeg" medium="image" fileSize="349828">
        <media:title type="plain">Illustration demonstrating gut-brain axis</media:title>
      </media:content>
    </item>
    <item>
      <title>The court said what it said, DC Circuit tells Norwich</title>
      <description>While the U.S. Supreme Court made it clear earlier this month in Hikma v. Amarin that skinny labels are still on the board for generics, the court didn’t resolve all disagreements over the generic carveouts.</description>
      <content:encoded>
        <![CDATA[While the U.S. Supreme Court made it clear earlier this month in <em>Hikma v. Amarin</em> that skinny labels are still on the board for generics, the court didn’t resolve all disagreements over the generic carveouts.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732229</guid>
      <pubDate>Mon, 29 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732229-the-court-said-what-it-said-dc-circuit-tells-norwich</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Geographic-regions/US/US-law-flag-gavel.webp?t=1593467765" type="image/png" medium="image" fileSize="1749746">
        <media:title type="plain">Judge's gavel with US flag</media:title>
      </media:content>
    </item>
    <item>
      <title>CINP 2026: Gut microbiota could predict antidepressant response</title>
      <description>The gut microbiota may be altered in people with depression as a result of treatment. These microorganisms reorganize differently in individuals who respond to therapy. In a multiomics study of antidepressant-naive patients presented at the 2026 World Congress of Neuropsychopharmacology (CINP), scientists from National Taiwan University found that patients who improved after antidepressant treatment maintained a more balanced and functional microbial ecosystem, recovered beneficial metabolites, and displayed blood-based biological signals that aligned with these changes.</description>
      <content:encoded>
        <![CDATA[The gut microbiota may be altered in people with depression as a result of treatment. These microorganisms reorganize differently in individuals who respond to therapy. In a multiomics study of antidepressant-naive patients presented at the 2026 World Congress of Neuropsychopharmacology (CINP), scientists from National Taiwan University found that patients who improved after antidepressant treatment maintained a more balanced and functional microbial ecosystem, recovered beneficial metabolites, and displayed blood-based biological signals that aligned with these changes.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732204</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732204-cinp-2026-gut-microbiota-could-predict-antidepressant-response</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Brain-gut-axis-connection-illustration.webp?t=1782743853" type="image/jpeg" medium="image" fileSize="349828">
        <media:title type="plain">Illustration demonstrating gut-brain axis</media:title>
      </media:content>
    </item>
    <item>
      <title>Pharmgen Science characterizes new H+/K+-ATPase inhibitors</title>
      <description>Pharmgen Science Inc. has patented H+/K+-ATPase inhibitors that are potentially useful for the treatment of asthma, esophagitis, Helicobacter pylori infection, gastroesophageal reflux disease, gastritis, peptic ulcer and more.</description>
      <content:encoded>
        <![CDATA[Pharmgen Science Inc. has patented H+/K+-ATPase inhibitors that are potentially useful for the treatment of asthma, esophagitis, <em>Helicobacter pylori</em> infection, gastroesophageal reflux disease, gastritis, peptic ulcer and more.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732197</guid>
      <pubDate>Fri, 26 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732197-pharmgen-science-characterizes-new-h-k-atpase-inhibitors</link>
    </item>
    <item>
      <title>New RIPK1 inhibitor protects from hepatic fibrosis</title>
      <description>Receptor-interacting protein kinase 1 (RIPK1) acts as a central signaling node regulating apoptosis, necroptosis and inflammatory pathways. Researchers from China Pharmaceutical University reported the discovery and preclinical characterization of LT-1339-553, a novel RIPK1 inhibitor, in models of schistosomiasis-induced hepatic fibrosis.</description>
      <content:encoded>
        <![CDATA[Receptor-interacting protein kinase 1 (RIPK1) acts as a central signaling node regulating apoptosis, necroptosis and inflammatory pathways. Researchers from China Pharmaceutical University reported the discovery and preclinical characterization of LT-1339-553, a novel RIPK1 inhibitor, in models of schistosomiasis-induced hepatic fibrosis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732192</guid>
      <pubDate>Fri, 26 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732192-new-ripk1-inhibitor-protects-from-hepatic-fibrosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/RIPK1-molecular-model.webp?t=1782483869" type="image/png" medium="image" fileSize="1086452">
        <media:title type="plain">3D molecular model illustration of RIPK1</media:title>
        <media:description type="plain">RIPK1</media:description>
      </media:content>
    </item>
    <item>
      <title>Spyre’s Skyline-UC double win lifts hopes for IBD antibody combos</title>
      <description>Spyre Therapeutics Inc.’s striking “two for two” data on ulcerative colitis (UC) candidates, SPY-001 and SPY-002, drew applause from multiple analysts, putting eyes on the Boston biotech’s upcoming top-line data of anti-IL-23 antibody SPY-003 – the third biologic module in a six-strong inflammatory bowel disease (IBD) lineup.</description>
      <content:encoded>
        <![CDATA[Spyre Therapeutics Inc.’s striking “two for two” data on ulcerative colitis (UC) candidates, SPY-001 and SPY-002, drew applause from multiple analysts, putting eyes on the Boston biotech’s upcoming top-line data of anti-IL-23 antibody SPY-003 – the third biologic module in a six-strong inflammatory bowel disease (IBD) lineup.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731905</guid>
      <pubDate>Wed, 17 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731905-spyres-skyline-uc-double-win-lifts-hopes-for-ibd-antibody-combos</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Gastrointestinal-system-illustration.webp?t=1769098607" type="image/jpeg" medium="image" fileSize="679694">
        <media:title type="plain">Gastrointestinal system</media:title>
      </media:content>
    </item>
    <item>
      <title>Zealand Pharma reports IL-23R antagonists</title>
      <description>Zealand Pharma A/S has identified new interleukin-23 receptor (IL-23R) antagonists potentially useful for the treatment of Crohn’s disease, ulcerative colitis, psoriasis and psoriatic arthritis.</description>
      <content:encoded>
        <![CDATA[Zealand Pharma A/S has identified new interleukin-23 receptor (IL-23R) antagonists potentially useful for the treatment of Crohn’s disease, ulcerative colitis, psoriasis and psoriatic arthritis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732002</guid>
      <pubDate>Wed, 17 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732002-zealand-pharma-reports-il-23r-antagonists</link>
    </item>
    <item>
      <title>Microbiota modulates the antidepressant effects of GLP-1 analogues</title>
      <description>Liraglutide, a glucagon-like peptide 1 (GLP-1) receptor agonist used in diabetes and obesity, could alleviate depression through a pathway that does not depend on the GLP-1 receptor but instead on the gut microbiota, since the treatment increases the presence of the bacterium Lactobacillus delbrueckii.</description>
      <content:encoded>
        <![CDATA[Liraglutide, a glucagon-like peptide 1 (GLP-1) receptor agonist used in diabetes and obesity, could alleviate depression through a pathway that does not depend on the GLP-1 receptor but instead on the gut microbiota, since the treatment increases the presence of the bacterium <em>Lactobacillus delbrueckii</em>. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731977</guid>
      <pubDate>Mon, 15 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731977-microbiota-modulates-the-antidepressant-effects-of-glp-1-analogues</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Lactobacillus-gram-positive-rod-shaped-lactic-acid-bacteria.webp?t=1781188632" type="image/jpeg" medium="image" fileSize="1095139">
        <media:title type="plain">Illustration of Lactobacillus</media:title>
        <media:description type="plain">Lactobacillus</media:description>
      </media:content>
    </item>
    <item>
      <title>Development of a BRAF V600E cholangiocarcinoma model in mice</title>
      <description>Researchers from Medizinische Hochschule Hannover and collaborators thus aimed to elucidate signaling adaptations following MAPK pathway inhibition in BRAFV 600E mutant cholangiocarcinoma (CCA) by generating a BRAF V600E-driven model of CCA.</description>
      <content:encoded>
        <![CDATA[Researchers from Medizinische Hochschule Hannover and collaborators thus aimed to elucidate signaling adaptations following MAPK pathway inhibition in BRAFV 600E mutant cholangiocarcinoma (CCA) by generating a BRAF V600E-driven model of CCA.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731859</guid>
      <pubDate>Fri, 12 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731859-development-of-a-braf-v600e-cholangiocarcinoma-model-in-mice</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Cholangiocarcinoma-Bile-Duct-Cancer.webp?t=1674573514" type="image/png" medium="image" fileSize="810777">
        <media:title type="plain">Illustration of cancer in the bile ducts</media:title>
      </media:content>
    </item>
    <item>
      <title>Microbiota modulates the antidepressant effects of GLP-1 analogues</title>
      <description>Liraglutide, a glucagon-like peptide 1 (GLP-1) receptor agonist used in diabetes and obesity, could alleviate depression through a pathway that does not depend on the GLP-1 receptor but instead on the gut microbiota, since the treatment increases the presence of the bacterium Lactobacillus delbrueckii. This symbiotic microorganism produces a lipid that modulates neuronal activity, normalizing the hyperactivation of brain regions in mice involved in emotional processing, which ultimately reduces depressive behaviors.</description>
      <content:encoded>
        <![CDATA[Liraglutide, a glucagon-like peptide 1 (GLP-1) receptor agonist used in diabetes and obesity, could alleviate depression through a pathway that does not depend on the GLP-1 receptor but instead on the gut microbiota, since the treatment increases the presence of the bacterium <em>Lactobacillus delbrueckii</em>. This symbiotic microorganism produces a lipid that modulates neuronal activity, normalizing the hyperactivation of brain regions in mice involved in emotional processing, which ultimately reduces depressive behaviors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731833</guid>
      <pubDate>Thu, 11 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731833-microbiota-modulates-the-antidepressant-effects-of-glp-1-analogues</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Lactobacillus-gram-positive-rod-shaped-lactic-acid-bacteria.webp?t=1781188632" type="image/jpeg" medium="image" fileSize="1095139">
        <media:title type="plain">Illustration of Lactobacillus</media:title>
        <media:description type="plain">Lactobacillus</media:description>
      </media:content>
    </item>
    <item>
      <title>Targeting TRIM54 mitigates liver injury in cirrhosis</title>
      <description>Researchers from Beijing University of Chinese Medicine described the role of TRIM54 in cirrhosis progression using two independent animal models of chronic liver injury – a DEN-induced rat model and a CCl4-induced mouse model of liver cirrhosis.</description>
      <content:encoded>
        <![CDATA[Researchers from Beijing University of Chinese Medicine described the role of TRIM54 in cirrhosis progression using two independent animal models of chronic liver injury – a DEN-induced rat model and a CCl4-induced mouse model of liver cirrhosis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731782</guid>
      <pubDate>Wed, 10 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731782-targeting-trim54-mitigates-liver-injury-in-cirrhosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-anatomy-on-medical-background.webp?t=1775850555" type="image/jpeg" medium="image" fileSize="591366">
        <media:title type="plain">Liver anatomy on medical background</media:title>
      </media:content>
    </item>
    <item>
      <title>Engitix seals GSK deal for targets to reverse liver fibrosis</title>
      <description>Extracellular matrix specialist Engitix Ltd. is teaming up with GSK plc to delve into the mechanisms underlying regression of fibrosis after treatment for chronic liver disease, and identify and validate new drug targets involved in this process.</description>
      <content:encoded>
        <![CDATA[Extracellular matrix specialist Engitix Ltd. is teaming up with GSK plc to delve into the mechanisms underlying regression of fibrosis after treatment for chronic liver disease, and identify and validate new drug targets involved in this process.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731798</guid>
      <pubDate>Tue, 09 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731798-engitix-seals-gsk-deal-for-targets-to-reverse-liver-fibrosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-7-7.webp?t=1657229334" type="image/png" medium="image" fileSize="759348">
        <media:title type="plain">Liver </media:title>
      </media:content>
    </item>
    <item>
      <title>Dual ABCB4/ABCB11 modulation shows promise in cholestatic disease models</title>
      <description>Researchers from Rectify Pharmaceuticals Inc. presented preclinical efficacy data on RTY-406, a novel dual-acting ABCB4/MDR3 and ABCB11/BSEP modulator, in animal models of primary sclerosing cholangitis.</description>
      <content:encoded>
        <![CDATA[Researchers from Rectify Pharmaceuticals Inc. presented preclinical efficacy data on RTY-406, a novel dual-acting ABCB4/MDR3 and ABCB11/BSEP modulator, in animal models of primary sclerosing cholangitis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731744</guid>
      <pubDate>Mon, 08 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731744-dual-abcb4-abcb11-modulation-shows-promise-in-cholestatic-disease-models</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-gallbladder-bile-ducts-anatomy.webp?t=1669131393" type="image/png" medium="image" fileSize="718435">
        <media:title type="plain">Liver anatomy illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Technique links non-coding mutations to disease genes they regulate</title>
      <description>Genome-wide association studies (GWAS) have identified multiple loci associated with complex diseases, but these are mostly on regulatory genes in the non-coding part of the genome and it has proved difficult to identify the effector genes that they control. Now, researchers in the U.K. have shown how single cell sequencing at scale can be used to precisely link non-coding GWAS loci to specific protein coding genes and cell types.</description>
      <content:encoded>
        <![CDATA[Genome-wide association studies (GWAS) have identified multiple loci associated with complex diseases, but these are mostly on regulatory genes in the non-coding part of the genome and it has proved difficult to identify the effector genes that they control. Now, researchers in the U.K. have shown how single cell sequencing at scale can be used to precisely link non-coding GWAS loci to specific protein coding genes and cell types.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731755</guid>
      <pubDate>Fri, 05 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731755-technique-links-non-coding-mutations-to-disease-genes-they-regulate</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/GI-system-with-DNA-scientific-background.webp?t=1774388477" type="image/jpeg" medium="image" fileSize="500606">
        <media:title type="plain">Gastrointestinal system with DNA, scientific background</media:title>
      </media:content>
    </item>
    <item>
      <title>Innate immunity and microbiome allied against pulmonary fibrosis</title>
      <description>The microbiome and a frontline innate antimicrobial sensor, Toll-like receptor 5 (TLR5), play an essential role in the development of idiopathic pulmonary fibrosis (IPF). A scientific collaboration led by researchers at the National Institute of Environmental Health Sciences has revealed how TLR5 protects against fibrosis through its ability to modulate the lung microbiome. Their study also shows that activating TLR5 protects against fibrosis and corrects pulmonary dysbiosis.</description>
      <content:encoded>
        <![CDATA[The microbiome and a frontline innate antimicrobial sensor, Toll-like receptor 5 (TLR5), play an essential role in the development of idiopathic pulmonary fibrosis (IPF). A scientific collaboration led by researchers at the National Institute of Environmental Health Sciences has revealed how TLR5 protects against fibrosis through its ability to modulate the lung microbiome. Their study also shows that activating TLR5 protects against fibrosis and corrects pulmonary dysbiosis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731651</guid>
      <pubDate>Thu, 04 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731651-innate-immunity-and-microbiome-allied-against-pulmonary-fibrosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Respiratory/Respiratory-lung-dna-drug-therapeutics.webp?t=1780586551" type="image/jpeg" medium="image" fileSize="588991">
        <media:title type="plain">Illustration of therapies for lung diseases</media:title>
      </media:content>
    </item>
    <item>
      <title>Technique links non-coding mutations to disease genes they regulate</title>
      <description>Genome-wide association studies (GWAS) have identified multiple loci associated with complex diseases, but these are mostly on regulatory genes in the non-coding part of the genome and it has proved difficult to identify the effector genes that they control. Now, researchers in the U.K. have shown how single cell sequencing at scale can be used to precisely link non-coding GWAS loci to specific protein coding genes and cell types.</description>
      <content:encoded>
        <![CDATA[Genome-wide association studies (GWAS) have identified multiple loci associated with complex diseases, but these are mostly on regulatory genes in the non-coding part of the genome and it has proved difficult to identify the effector genes that they control. Now, researchers in the U.K. have shown how single cell sequencing at scale can be used to precisely link non-coding GWAS loci to specific protein coding genes and cell types.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731544</guid>
      <pubDate>Wed, 03 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731544-technique-links-non-coding-mutations-to-disease-genes-they-regulate</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/GI-system-with-DNA-scientific-background.webp?t=1774388477" type="image/jpeg" medium="image" fileSize="500606">
        <media:title type="plain">Gastrointestinal system with DNA, scientific background</media:title>
      </media:content>
    </item>
    <item>
      <title>CRISPR-based approach fights pathogenic &lt;em&gt;E. coli&lt;/em&gt; </title>
      <description>Shiga toxin-producing Escherichia coli (STEC) represents a public health threat that can lead to serious problems, such as bloody diarrhea and hemolytic uremic syndrome in children in up to 10%-15% of cases. Antibiotics that normally combat diarrhea are not recommended for STEC infections and patients are usually treated only for symptomatology. Now, French researchers from Eligo Bioscience SA and their collaborators have published a paper on a CRISPR-based antimicrobial approach, EB-003.</description>
      <content:encoded>
        <![CDATA[Shiga toxin-producing <em>Escherichia coli</em> (STEC) represents a public health threat that can lead to serious problems, such as bloody diarrhea and hemolytic uremic syndrome in children in up to 10%-15% of cases. Antibiotics that normally combat diarrhea are not recommended for STEC infections and patients are usually treated only for symptomatology. Now, French researchers from Eligo Bioscience SA and their collaborators have published a paper on a CRISPR-based antimicrobial approach, EB-003.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731670</guid>
      <pubDate>Wed, 03 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731670-crispr-based-approach-fights-pathogenic-eme-coli-em</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/E-coli-Thom-Leach.webp?t=1709224791" type="image/jpeg" medium="image" fileSize="391680">
        <media:title type="plain">Illustration of E. coli with window showing DNA</media:title>
        <media:description type="plain">E.coli. Credit: Thom Leach. License: CC by SA</media:description>
      </media:content>
    </item>
    <item>
      <title>TAK1 emerges as a therapeutic target in MASLD</title>
      <description>Transforming growth factor-β-activated kinase 1 (TAK1) is a crucial central signaling molecule of hepatic cell death, inflammation and fibrogenesis through NF-κB and MAPK in metabolic dysfunction-associated steatotic liver disease (MASLD). Its pharmacological inhibition using the TAK1 inhibitor HS-276 was tested in vivo in a murine model of diet-induced MASLD.</description>
      <content:encoded>
        <![CDATA[Transforming growth factor-β-activated kinase 1 (TAK1) is a crucial central signaling molecule of hepatic cell death, inflammation and fibrogenesis through NF-κB and MAPK in metabolic dysfunction-associated steatotic liver disease (MASLD). Its pharmacological inhibition using the TAK1 inhibitor HS-276 was tested in vivo in a murine model of diet-induced MASLD.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731600</guid>
      <pubDate>Wed, 03 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731600-tak1-emerges-as-a-therapeutic-target-in-masld</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Liver-research-investigation-microscope.webp?t=1780498148" type="image/jpeg" medium="image" fileSize="237511">
        <media:title type="plain">Illustration of doctors examining a liver with magnifier and microscope</media:title>
      </media:content>
    </item>
    <item>
      <title>GPR119 activation ameliorates alcohol-related liver disease</title>
      <description>There is a growing consensus that alcohol-related liver disease (ALD) should be considered a metabolic disorder under the influence of the gut-liver axis. Metabolome data have highlighted fatty acid-activated G protein-coupled receptors (GPCRs) as the main affected pathways, where the relationship of G-protein-coupled receptor 119 (GPR119) with ALD remains unexplored.</description>
      <content:encoded>
        <![CDATA[There is a growing consensus that alcohol-related liver disease (ALD) should be considered a metabolic disorder under the influence of the gut-liver axis. Metabolome data have highlighted fatty acid-activated G protein-coupled receptors (GPCRs) as the main affected pathways, where the relationship of G-protein-coupled receptor 119 (GPR119) with ALD remains unexplored.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731599</guid>
      <pubDate>Wed, 03 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731599-gpr119-activation-ameliorates-alcohol-related-liver-disease</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/liver-cirrhosis-fibrosis.webp?t=1712672928" type="image/jpeg" medium="image" fileSize="823791">
        <media:title type="plain">Photomicrograph of liver biopsy in a patient with cirrhosis. </media:title>
        <media:description type="plain">Photomicrograph of liver biopsy in a patient with cirrhosis, showing bridging septal fibrosis and regenerative nodules. Stained with trichrome to highlight fibrosis (blue).</media:description>
      </media:content>
    </item>
    <item>
      <title>ATGL inhibition reshapes immunometabolism in liver fibrosis</title>
      <description>Adipose triglyceride lipase (ATGL), a central mediator of triglyceride hydrolysis and fatty acid mobilization, modulates hepatic lipid homeostasis and metabolic signaling pathways that contribute to the activation of fibrogenic responses.</description>
      <content:encoded>
        <![CDATA[Adipose triglyceride lipase (ATGL), a central mediator of triglyceride hydrolysis and fatty acid mobilization, modulates hepatic lipid homeostasis and metabolic signaling pathways that contribute to the activation of fibrogenic responses.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731598</guid>
      <pubDate>Wed, 03 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731598-atgl-inhibition-reshapes-immunometabolism-in-liver-fibrosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-doctor.webp?t=1589217270" type="image/png" medium="image" fileSize="244160">
        <media:title type="plain">Doctor pointing at liver</media:title>
      </media:content>
    </item>
    <item>
      <title>SR-1891 achieves prolonged HBV suppression with one dose</title>
      <description>Researchers from Ospedale San Raffaele presented the preclinical characterization of SR-1891, a long-acting capsid assembly modulator (CAM) in models of chronic hepatitis B. In Hepa D38 cells, the compound exhibited EC50 and EC90 values of 0.2 and 0.8 nM, respectively, without any detectable cytotoxicity.</description>
      <content:encoded>
        <![CDATA[Researchers from Ospedale San Raffaele presented the preclinical characterization of SR-1891, a long-acting capsid assembly modulator (CAM) in models of chronic hepatitis B. In Hepa D38 cells, the compound exhibited EC50 and EC90 values of 0.2 and 0.8 nM, respectively, without any detectable cytotoxicity.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731594</guid>
      <pubDate>Wed, 03 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731594-sr-1891-achieves-prolonged-hbv-suppression-with-one-dose</link>
    </item>
    <item>
      <title>Hanmi, Haisco win billion-dollar partnerships with Eli Lilly</title>
      <description>Hanmi Pharmaceutical Co. Ltd. secured a $1.26 billion deal with Eli Lilly and Co. to out-license ex-Korea rights to sonefpeglutide (HM-15912), a Lapscovery-based glucagon-like peptide-2 analog in development for multiple indications, including an ongoing phase II study of short bowel syndrome. It was one of two billion-dollar Asian company deals signed by Lilly on June 1, with the second transaction involving Haisco Pharmaceutical Group Co. Ltd., of Beijing.</description>
      <content:encoded>
        <![CDATA[Hanmi Pharmaceutical Co. Ltd. secured a $1.26 billion deal with Eli Lilly and Co. to out-license ex-Korea rights to sonefpeglutide (HM-15912), a Lapscovery-based glucagon-like peptide-2 analog in development for multiple indications, including an ongoing phase II study of short bowel syndrome. It was one of two billion-dollar Asian company deals signed by Lilly on June 1, with the second transaction involving Haisco Pharmaceutical Group Co. Ltd., of Beijing.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731645</guid>
      <pubDate>Tue, 02 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731645-hanmi-haisco-win-billion-dollar-partnerships-with-eli-lilly</link>
      <media:content url="https://www.bioworld.com/ext/resources/BW-source/2026/Hanmi-signage-6-1.webp?t=1780342948" type="image/jpeg" medium="image" fileSize="195343">
        <media:title type="plain">Hanmi signage</media:title>
        <media:description type="plain">Credit: Hanmi Pharmaceutical Co. Ltd.</media:description>
      </media:content>
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