Journal Article

Phosphorylation of FADD is critical for sensitivity to anticancer drug-induced apoptosis

Keiji Shimada, Syuichi Matsuyoshi, Mitsutoshi Nakamura, Eiwa Ishida, Munehiro Kishi and Noboru Konishi

in Carcinogenesis

Volume 25, issue 7, pages 1089-1097
Published in print July 2004 | ISSN: 0143-3334
Published online July 2004 | e-ISSN: 1460-2180 | DOI: http://dx.doi.org/10.1093/carcin/bgh130
Phosphorylation of FADD is critical for sensitivity to anticancer drug-induced apoptosis

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FADD has been shown to be phosphorylated at Ser194 at the G2/M transition of the cell cycle. Here we have investigated the contribution of this phosphorylation to apoptosis induced by anticancer drugs in two human prostate cancer cell lines, LNCaP and DU145. Both were arrested at G2/M and FADD was found to be phosphorylated at Ser194 on treatment with paclitaxel. Inhibition of paclitaxel-induced c-jun NH2-terminal kinase (JNK) activation by treatment with a specific inhibitor, SP600125, or overexpression of a dominant-negative mutant form of upstream kinases, MEK kinase 1 (MEKK1) and mitogen-activated protein kinase kinase (MKK) 7, significantly reduced the increase in phosphorylated FADD. It is noteworthy that pretreatment with paclitaxel significantly up-regulated MEKK1 expression, resulting in enhancement of etoposide- or cisplatin-induced MEKK1/MKK7-dependent JNK activation and apoptosis in LNCaP and DU145 cells. Interestingly, MEKK1 up-regulation and the synergistic effects of paclitaxel on anticancer drug-induced apoptosis were abolished by overexpression of mutant FADD (Ser194→Ala). The results clearly show that FADD phosphorylation at Ser194 affects functions both upstream and downstream of the MEKK1/MKK7/JNK1 pathway and is closely associated with chemosensitivity in prostate cancer cells. This is the first report indicating that phosphorylated FADD plays an essential role in the mechanisms of amplifications of chemotherapy-induced apoptosis.

Keywords: MEKK, MEK kinase; MKK, MAP kinase kinase; MAP, mitogen-activated protein; JNK, c-jun NH2-terminal kinase; FADD, Fas-associated death domain-containing protein; PBS, phosphate-buffered saline; β-gal, β-galactosidase

Journal Article.  4634 words.  Illustrated.

Subjects: Clinical Cytogenetics and Molecular Genetics

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