Study reveals how melanoma silences the skin’s natural antitumor defense
Peer-Reviewed Publication
Updates every hour. Last Updated: 22-Oct-2026 23:16 ET (23-Oct-2026 03:16 GMT/UTC)
A new study by researchers from the Atopy (Allergy) Research Center of the Juntendo University Graduate School of Medicine, Japan, led by Professor François Niyonsaba, has uncovered an “arms race” between melanoma cells and the surrounding skin cells called keratinocytes. Keratinocytes produce LL-37, an antimicrobial peptide that can directly suppress melanoma growth and spread. Melanoma cells escape this protective mechanism by transferring hsa-miR-221-5p through exosomes to keratinocytes in their vicinity, reducing their LL-37 production.
A new study published in Biomedical Analysis reports a protein-coated nanoparticle platform that combines the powerful light-to-heat conversion ability of copper sulfide with the biological compatibility of albumin, offering a potential strategy for safer photothermal cancer therapy.
One of Australia's largest real world studies of younger adults with advanced bowel cancer has identified important differences between cancers diagnosed before and after the age of 50, which could help doctors tailor treatments for younger adults more effectively.
Borrowing from the study of complex systems like flocks of birds and microbial communities, UChicago researchers built AI tools that compare the spatial organization of tumors — a step toward personalized cancer treatment.
MUSC Hollings Cancer Center researchers have uncovered a new way to exploit a weakness in triple-negative breast cancer (TNBC), an aggressive form of breast cancer that often develops resistance to chemotherapy. The team discovered a previously unknown role for the protein LOX inside cancer cells, where it helps to support energy production, healthy mitochondria and other processes the cells rely on to survive.
When researchers blocked LOX, the cancer cells became vulnerable but adapted by relying more heavily on a backup survival pathway controlled by a protein called DHODH. The team, led by Hollings researcher Ozgur Sahin, Ph.D., turned that adaptation against the cancer with a “one-two punch”: first blocking LOX to weaken the cells, then blocking DHODH to cut off their escape route. The combination significantly blocked tumor growth across multiple patient-derived models without chemotherapy and showed potential advantages over pairing the LOX-blocking drug with standard chemotherapy.
The findings are still preclinical, but they point toward a potential strategy for treating chemotherapy-resistant TNBC while one day reducing reliance on chemotherapy and its serious side effects. The researchers also found evidence that LOX and DHODH could potentially serve as biomarkers to help identify patients most likely to benefit. The team is now developing a newer LOX-blocking drug and completing studies needed to move the approach toward testing in people.