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BioWorld - Friday, February 6, 2026
Home » Keywords » skin cancer

Items Tagged with 'skin cancer'

ARTICLES

Cancer

New Raf kinase B degradation inducers disclosed in Shenzhen Targetrx patent

Dec. 24, 2025
Shenzhen Targetrx Inc. has divulged proteolysis targeting chimera (PROTAC) compounds comprising a cereblon (CRBN)-binding moiety covalently linked to Raf kinase B (V600E mutant)-targeting moiety through linker reported to be useful for the treatment of cancer.
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Cancer

Shanghai Xianxiang Medical Technology divulges new EGFR degradation inducers

Dec. 23, 2025
Shanghai Xianxiang Medical Technology Co. Ltd. has synthesized proteolysis targeting chimera (PROTAC) compounds comprising a cereblon (CRBN)-binding moiety coupled to an EGFR (HER1; erbB1) mutant-targeting moiety through a linker reported to be useful for the treatment of cancer.
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Cancer

Sunrise Oncology describes new PDE3A/SLFN12 interaction inducers

Nov. 20, 2025
Sunrise Oncology (Hong Kong) Ltd. has identified molecular glues acting as phosphodiesterase PDE3A/SLFN12 interaction inducers reported to be useful for the treatment of cancer.
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Cancer

Aurigene Oncology describes new SMARCA2 and SMARCA4 degradation inducers

Oct. 15, 2025
Aurigene Oncology Ltd. has identified proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase protein binding moiety covalently linked to probable global transcription activator SNF2L2 (SMARCA2; BAF190B; SNF2-α) and/or transcription activator BRG1 (SMARCA4; BAF190A; SNF2-β) binding moieties through a linker reported to be useful for the treatment of cancer.
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Concept art for targeting cancer
Immuno-oncology

Dual PD-L1 NAMPT inhibitor gives one-two anticancer punch

Oct. 10, 2025
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While immunotherapy targeting PD-1 or its ligand PD-L1 has transformed cancer treatment by overcoming T-cell exhaustion, only a minority of patients achieves durable responses after treatment.
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Concept art for targeting cancer
Immuno-oncology

Pan-cancer oncolytic virus expressing FLT3 ligand

Aug. 22, 2025
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Oncolytic viruses are being actively explored as cancer therapies because they preferentially infect tumor cells and cause their lysis. At the same time, the viruses can accommodate transgenes that can stimulate anti-cancer responses in the local tumor microenvironment.
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Cancer

The Ohio State University divulges new MPS1 inhibitors

Aug. 13, 2025
The Ohio State University has synthesized dual specificity protein kinase TTK (MPS1; MPS1L1) inhibitors reported to be useful for the treatment of cancer.
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Cancer

C4 Therapeutics patents new B-Raf V600E mutant degradation inducers

May 21, 2025
C4 Therapeutics Inc. has disclosed proteolysis targeting chimera (PROTAC) compounds comprising a cereblon (CRBN) E3 ubiquitin ligase-binding moiety covalently linked to a Raf kinase B (V600E mutant)-targeting moiety through a linker. They are reported to be useful for the treatment of cancer.
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Illustration of stent angioplasty balloon in artery

UK’s NICE seeks to apply price pressures on drug-eluting stents

May 6, 2025
By Mark McCarty
The U.K. National Institute for Health and Care Excellence (NICE) opened a late-stage assessment for drug-eluting stents (DES) with an eye toward costs, advising clinicians that they should implant the least expensive DES unit that is clinically appropriate for that patient while the assessment is underway.
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Photo of magnifying glass inspecting moles on person's back
Biomarkers

INSM1 is highly sensitive marker in primary and metastatic Merkel cell carcinoma

April 4, 2025
The detection of metastases in Merkel cell carcinoma (MCC) requires additional testing, such as pancytokeratin (panCK) or CK20, with no guarantee of success. Recent findings have identified transcription factor SOX11 and insulinoma-associated protein 1 (INSM1) as sensitive nuclear neuroendocrine markers, but their usefulness in MCC has not been proven.
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