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Apoptosis and melanoma chemoresistance

Journal

ONCOGENE
Volume 22, Issue 20, Pages 3138-3151

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.onc.1206454

Keywords

skin cancer; drug resistance; apoptosis; cancer therapy; chemotherapeutic targets

Funding

  1. NCI NIH HHS [P30 CA008748] Funding Source: Medline

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Melanoma is the most aggressive form of skin cancer and is notoriously resistant to all current modalities of cancer therapy. A large set of genetic, functional and biochemical studies suggest that melanoma cells become 'bullet proof' against a variety of chemotherapeutic drugs by exploiting their intrinsic resistance to apoptosis and by reprogramming their proliferation and survival pathways during melanoma progression. In recent years, the identification of molecules involved in the regulation and execution of apoptosis, and their alteration in melanoma, have provided new insights into the molecular basis for melanoma chemoresistance. With this knowledge in hand, the challenge is now to devise strategies potent enough to compensate or bypass these cell death defects and improve the actual poor prognosis of patients at late stages of the disease.

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