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Down-regulation of GADD45A enhances chemosensitivity in melanoma

机译:GADD45A的下调增强了黑色素瘤的化学敏感性

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摘要

Melanoma is a malignant skin cancer with considerable drug resistance. Increased expression of DNA repair genes have been reported in melanoma, and this contributes to chemotherapy resistance. GADD45A is involved in DNA repair, cell cycle arrest and apoptosis in response to physiologic or environmental stresses. In this study, we investigated the role of GADD45A in chemotherapy response. Firstly, the mRNA expression of profiled DNA repair genes in cisplatin-treated melanoma cells was detected by RT2 profilerTM PCR array. We found the expression of GADD45A upregulated in a dose- and time- dependent manner. In addition, suppression of GADD45A sensitized melanoma cells to cisplatin and enhanced cisplatin-induced DNA damage. Flow cytometry revealed that downregulating GADD45A released cells from cisplatin-induced G2/M arrest and increased apoptosis. By using a MEK inhibitor, GADD45A was shown to be regulated by MAPK-ERK pathway following cisplatin treatment. Thus, the induction of GADD45A might play important roles in chemotherapy response in human melanoma cancer and could serve as a novel molecular target for melanoma therapy.
机译:黑色素瘤是一种具有相当大耐药性的恶性皮肤癌。黑色素瘤中已经报道了DNA修复基因表达的增加,这有助于化疗耐药性。 GADD45A参与DNA修复,细胞周期停滞和细胞凋亡,以响应生理或环境压力。在这项研究中,我们调查了GADD45A在化疗反应中的作用。首先,通过RT 2 profiler TM PCR芯片检测顺铂处理的黑色素瘤细胞中DNA修复基因的mRNA表达。我们发现GADD45A的表达呈剂量和时间依赖性上调。此外,GADD45A抑制黑素瘤细胞对顺铂敏感,并增强了顺铂诱导的DNA损伤。流式细胞仪表明,下调GADD45A释放了顺铂诱导的G2 / M阻滞并增加了细胞凋亡。通过使用MEK抑制剂,表明顺铂处理后GADD45A受MAPK-ERK途径调节。因此,GADD45A的诱导可能在人类黑素瘤癌症的化学治疗反应中起重要作用,并且可以作为黑素瘤治疗的新分子靶标。

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