Augmenting chemosensitivity of malignant melanoma tumors via proteasome inhibition: implication for bortezomib (VELCADE, PS-341) as a therapeutic agent for malignant melanoma.

Amiri KI, Horton LW, LaFleur BJ, Sosman JA, Richmond A
Cancer Res. 2004 64 (14): 4912-8

PMID: 15256463 · DOI:10.1158/0008-5472.CAN-04-0673

Melanoma poses a great challenge to patients, oncologists, and biologists because of its nearly universal resistance to chemotherapy. Many studies have shown that nuclear factor kappaB is constitutively activated in melanoma, thereby promoting the proliferation of melanoma cells by inhibiting the apoptotic responses to chemotherapy. Nuclear factor kappaB activity is regulated by phosphorylation and subsequent degradation of inhibitor of nuclear factor kappaB by the ubiquitin-proteasome pathway. In this study, we show that the novel proteasome inhibitor, bortezomib, inhibited the growth of melanoma cells in vitro at a concentration range of 0.1-10 nM and in combination with the chemotherapeutic agent temozolomide, the inhibitory effect on melanoma cell growth was even more prominent. Data from a murine model showed reduced tumor growth when bortezomib was administered to human melanoma tumors. Strikingly, animals receiving bortezomib in combination with temozolomide achieved complete remission of palpable tumors after only 30 days of therapy, lasting >200 days. Our data indicate strongly that bortezomib in combination with chemotherapeutic agents should be studied additionally for the treatment of melanoma.

MeSH Terms (22)

Active Transport, Cell Nucleus Animals Antineoplastic Agents Antineoplastic Combined Chemotherapy Protocols Apoptosis Boronic Acids Bortezomib Cell Division Cell Line, Tumor Dacarbazine Drug Synergism Female Gene Expression Humans Melanoma Mice Mice, Inbred BALB C Neovascularization, Pathologic NF-kappa B Protease Inhibitors Pyrazines Temozolomide

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