Toxicology and applied pharmacology · 2018
Triptolide enhances chemotherapeutic efficacy of antitumor drugs in non-small-cell lung cancer cells by inhibiting Nrf2-ARE activity.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Zhu Jiayu, Wang Huihui, Chen Feng, Lv Hang, Xu Zijin, Fu Jingqi, Hou Yongyong, Xu Yuanyuan, Pi Jingbo
Аннотация
Non-small cell lung cancer (NSCLC) has a high mortality rate worldwide. Various treatments strategies have been used against NSCLC including individualized chemotherapies, but innate or acquired cancer cell drug resistance remains a major obstacle. Recent studies revealed that the Kelch-like ECH associated protein 1/Nuclear factor erythroid 2-related factor 2 (Keap1/Nrf2) pathway is intimately involved in cancer progression and chemoresistance. Thus, antagonizing Nrf2 would seem to be a viable strategy in cancer therapy. In the present study a traditional Chinese medicine, triptolide, was identified that markedly inhibited expression and transcriptional activity of Nrf2 in various cancer cells, including NSCLC and liver cancer cells. Consequently, triptolide made cancer cells more chemosensitivity toward antitumor drugs both in vitro and in a xenograft tumor model system using lung carcinoma cells. These results suggest that triptolide blocks chemoresistance in cancer cells by targeting the Nrf2 pathway. Triptolide should be further investigated in clinical cancer trials.
Предметные рубрики MeSH
A549 CellsAnimalsAntineoplastic AgentsAntineoplastic Agents, AlkylatingAntineoplastic Combined Chemotherapy ProtocolsAntioxidant Response ElementsCarcinoma, Non-Small-Cell LungDiterpenesDose-Response Relationship, DrugDrug Resistance, NeoplasmEpoxy CompoundsHep G2 CellsHumansLung NeoplasmsMaleMiceMice, Inbred C57BLNF-E2-Related Factor 2PhenanthrenesTreatment OutcomeTumor BurdenXenograft Model Antitumor Assays