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BioWorld - Thursday, May 28, 2026
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Photo of Stichodactyla helianthus anemone underwater
Aging

Sea anemone venom acts as a senolytic tool against cancer

Jan. 13, 2026
By Mar de Miguel
No Comments
The sea anemone Stichodactyla helianthus, which carpets the Caribbean seafloor, may hold the key to eliminating the senescent cells that survive cancer therapy. A collaboration led by Spanish scientists across several international research centers has discovered a new type of toxin that selectively eliminates senescent cancer cells.
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Diagnostics

Crinetics Pharmaceuticals discovers new SSTR2 non-peptide-drug conjugates

Jan. 13, 2026
Crinetics Pharmaceuticals Inc. has described drug conjugates consisting of a non-peptide moiety targeting G protein-coupled receptors (GPCRs) covalently linked to a chemotherapeutic moiety through a linker reported to be useful for the diagnosis and treatment of cancer.
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Swiss currency
Immune

Tecregen raises seed round to progress thymus-restoring biologics

Jan. 12, 2026
By Nuala Moran
No Comments
Newco Tecregen AG has raised CHF10 million (US$12.5 million) to advance a novel way of regenerating the thymus in order to boost T-cell production and stimulate recovery of the immune system following stem cell transplants and chemo- and radiotherapy.
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Cancer

New CDK2 degraders disclosed in Triana Biomedicines patent

Jan. 12, 2026
Triana Biomedicines Inc. has divulged protein/nucleic acid degraders acting as cyclin-dependent kinase 2 (CDK2) degraders reported to be useful for the treatment of cancer.
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Endocrine/metabolic

Monash University describes new melanocortin MC5 receptor agonists

Jan. 12, 2026
Monash University has identified cyclic peptides acting as melanocortin MC5 receptor (MC5R) agonists reported to be useful for the treatment of diabetes, obesity, cardiomyopathy, heart failure, renal disorders, Rabson Mendenhall syndrome, Donohue syndrome and lipodystrophy.
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Hematologic

Linkcure Therapeutics divulges new WIZ degradation inducers

Jan. 12, 2026
Linkcure Therapeutics has synthesized molecular glue degraders acting as zinc finger protein 803 (ZNF803; WIZ) degradation inducers reported to be useful for the treatment of sickle cell anemia and β-thalassemia.
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Endocrine/metabolic

Hanmi Pharmaceutical patents new GLP-1R/GCGR/GDIR agonists

Jan. 12, 2026
Hanmi Pharmaceutical Co. Ltd. has disclosed polypeptides acting as triple agonists of glucagon like peptide 1 receptor (GLP-1R), glucagon receptor (GCGR) and glucose-dependent insulinotropic receptor (GDIR; GPR119) reported to be useful for the treatment of dyslipidemia.
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Eye and DNA
Ocular

RNA-targeting CRISPR-Cas13 and engineered U1 correct variants in Stargardt disease

Jan. 12, 2026
No Comments
Disruption of alternative splicing can generate abnormal mRNA variants, producing nonfunctional proteins or triggering nonsense-mediated decay, and is implicated in many splicing-related diseases. Therapeutic approaches that modulate splicing, therefore, hold promise to redirect aberrant transcripts toward normal isoforms and reestablish functional protein expression.
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Antibiotic resistant bacteria inside a biofilm
Infection

Coumarin derivative exhibits potent antibiofilm activity

Jan. 12, 2026
No Comments
The treatment of Pseudomonas aeruginosa infections is significantly challenged by the pathogen’s diverse resistance mechanisms, with biofilm formation being a key driver of antibiotic tolerance. Furthermore, P. aeruginosa pathogenicity is amplified by virulence factors that both evade host defenses and facilitate biofilm development.
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3D illustration of cancer in crosshairs
Cancer

ADAR1-i-124 switches on antitumor immunity

Jan. 12, 2026
No Comments
Adenosine deaminase acting on RNA (ADAR) is the enzyme responsible for adenosine-to-inosine (A-to-I) RNA editing, a process essential for regulating how cells respond to double-stranded RNA. ADAR1 generates two isoforms, p150 and p110, with distinct roles in cancer biology. Researchers from the Wistar Institute of Anatomy & Biology reported the preclinical characterization of ADAR1-i-124, an ADAR1 inhibitor designed for the treatment of cancer.
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