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BioWorld - Sunday, December 21, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Feb. 26, 2025

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Human breast cancer cells

Tumor cell cooperation could be therapeutic vulnerability

In general, tumor cells embody the idea of “the survival of the fittest” gone out of control. Tumor cells outcompete their normal brethren with their uncontrolled growth; and the inside of a tumor is a fiercely competitive environment where over time, the most aggressive clones take over. But research published online in Nature on Feb. 19, 2025, has discovered that cancer cells cooperate as well as compete. Read More

OCT-598 enhances chemotherapeutic efficacy in gastric cancer

Patients with metastatic or unresectable gastric cancer are usually given 5-fluorouracil (5-FU) and platinum-based chemotherapy, but patients with advance disease usually have a poor prognosis. The use of chemotherapy increased the levels of cyclooxygenase-2 in tumor cells, which in turn increase the levels of prostaglandin E2 (PGE2) in the tumor microenvironment. When PGE2 binds to their receptors EP1 to EP4 on immune cells, it triggers an immunosuppressive tumor microenvironment. The use of the EP2 and EP4 dual antagonist OCT-598 was tested in the preclinical setting for gastric cancer. Read More
Person testing glucose level

Pre-IND meeting guides path forward for ITOL-102 for type 1 diabetes

Kadimastem Ltd. and Itolerance Inc. have held a type B pre-IND meeting with the FDA regarding the development of ITOL-102, an investigational biologic for the treatment and potential cure of type 1 diabetes that would not require life-long chronic immune system suppression. It comprises Kadimastem’s allogenic human stem cell-derived pancreatic islets (Isletrx cells) combined with Itolerance’s immunomodulator, ITOL-100. Read More
Illustration of cancer in the pancreas

Silexion completes study of SIL-204 in orthotopic pancreatic cancer models

Silexion Therapeutics Corp. has completed its initial study evaluating SIL-204 in orthotopic pancreatic cancer models. SIL-204 is a next-generation siRNA candidate designed to target a broad range of KRAS mutations. Read More

Restoring GJB2 expression rescues hereditary hearing loss

The most common form of hereditary deafness in humans is caused by mutations in the GJB2 gene, which encodes the gap junction protein connexin 26. That regulates the transport of potassium and metabolites between inner ear cells. The coding sequence of this gene fits in an adenovirus-associated vector (AAV), making it an attractive approach for gene therapy. Read More
World trade illustration

Five med-tech trends to watch in 2025

The Clarivate Medtech Trends to Watch in 2024 report noted the resilience of the medtech sector in the face of changing macroeconomic factors and the preparation required to navigate the market’s many complexities. It is likely that 2025 will be no different. Read More

First-in-class GSPT-1 molecular glue for liver cancer reported

Researchers from Captor Therapeutics Inc. presented the preclinical characterization of CT-01, a first-in-class GSPT-1 targeted degrader under investigation for the treatment of hepatocellular carcinoma. Read More

YAP-TEAD and TAZ-TEAD inhibitors revealed in Merck KGaA patent

Merck KGaA has patented substituted bicyclic transcriptional coactivator YAP1/transcriptional enhancer factor (TEAD) and/or TAZ/TED interaction inhibitors reported to be useful for the treatment of cancer. Read More

CCR9 blockade reestablishes gastrointestinal equilibrium in IBD

Researchers from Sunrock Biopharma SL presented preclinical data on SRB-1, a CCR9-depleting antibody aimed to restore immune homeostasis in patients with inflammatory bowel disease. Read More
Colorized scanning electron micrograph of E. coli bacteria.

CARB-X funds Immunethep’s conjugated peptide-based vaccine for E. coli infections

CARB-X (Combating Antibiotic-Resistant Bacteria Biopharmaceutical Accelerator) has announced it will award US$2 million to Immunethep SA to develop a conjugated peptide-based vaccine to prevent infections from all invasive serotypes of Escherichia coli. Read More

Astrazeneca reports anthracycline derivatives and conjugates

Astrazeneca has identified anthracycline compounds and antibody-drug conjugates consisting of an antibody covalently bound to anthracycline derivatives reported to be useful for the treatment of cancer. Read More

MA-242 exerts potent antitumor activity by modulating metabolic pathways in breast cancer

Previous research revealed that nuclear factor of activated T cells 1 (NFAT1) is a novel regulator of the mouse double minute 2 homolog (MDM2) oncogene, which acts by directly binding to the MDM2 P2 promoter and as such, enhancing MDM2 transcription independent of p53. Researchers from the University of Houston and Baylor College of Medicine presented preclinical data for MA-242, a dual inhibitor of MDM2 and NFAT1, being developed for the treatment of cancer. Read More
Illustration of motor neuron connecting to muscle fiber

FKBP12 ligand MP-010 shows neuroprotective effects in model of ALS

Researchers from Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Miramoon Pharma SL and affiliated organizations published the preclinical characterization of FKBP12 ligand MP-010 and evaluated its efficacy in models of amyotrophic lateral sclerosis. Read More

Terremoto Biosciences patents AKT1 inhibitors for cancer

Terremoto Biosciences Inc. has synthesized new 3H-imidazo[4,5-b]pyridine compounds acting as RAC-α serine/threonine-protein kinase (AKT1; PKB-α) inhibitors reported to be useful for the treatment of cancer. Read More

Enanta Pharmaceuticals discloses c-KIT inhibitors

Enanta Pharmaceuticals Inc. has developed mast/stem cell growth factor receptor kit (KIT; c-KIT; CD117) inhibitors reported to be useful for the treatment of cancer, autoimmune disease, fibrosis, pulmonary arterial hypertension, irritable bowel syndrome, inflammatory, dermatological and respiratory disorders, among others. Read More
Art concept for drug research

Bridgene and Takeda collaborate in immunology and neurology

Bridgene Biosciences Inc. has signed a strategic collaboration and licensing agreement with Takeda Pharmaceutical Co. Ltd. to discover small-molecule drug candidates against targets in immunology and neurology. Read More

Shanghai Pharmaceuticals describes D2 and D3 receptor agonists

Shanghai Pharmaceuticals Holding Co. Ltd. has disclosed aza-ergoline derivatives acting as dopamine D2 receptor and/or D3 receptor agonists reported to be useful for the treatment of attention deficit hyperactivity disorder (ADHD), depression, erectile dysfunction, substance abuse and dependence, restless legs syndrome, schizophrenia, Parkinson’s and Alzheimer’s disease, among others. Read More

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