Triptolide enhances carboplatin-induced apoptosis by inhibiting nucleotide excision repair (NER) activity in melanoma

雷公藤内酯醇通过抑制黑色素瘤中的核苷酸切除修复 (NER) 活性增强卡铂诱导的细胞凋亡

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作者:Geng Wang, Hongmin Guo, Yan Ren, Weiyi Chen, Yixuan Wang, Jianing Li, Hua Liu, Jingjun Xing, Yanru Zhang, Na Li

Discussion

This study reveals the NER inhibitor TPL which has great potential in treating melanoma, either alone or in combination with CBP.

Methods

Melanoma cell lines and xenograft mouse model were used to uncover the antitumor effects and the underlying molecular mechanisms of the alone or combined treatment of TPL and CBP in melanoma. Cell viability, migration, invasion, apoptosis, and DNA damage were detected by conventional methods. The rate-limiting proteins of the NER pathway were quantitated using PCR and Western blot. Fluorescent reporter plasmids were used to test the NER repair capacity.

Results

Our results showed that the presence of TPL in CBP treatment could selectively inhibit NER pathway activity, and TPL exerts a synergistic effect with CBP to inhibit viability, migration, invasion, and induce apoptosis of A375 and B16 cells. Moreover, combined treatment with TPL and CBP significantly inhibited tumor progression in nude mice by suppressing cell proliferation and inducing apoptosis.

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