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芹菜素通过抑制肿瘤干细胞增强顺铂对肺癌的抗肿瘤作用。

Apigenin Enhanced Antitumor Effect of Cisplatin in Lung Cancer via Inhibition of Cancer Stem Cells.

机构信息

Department of Respiratory Medicine, Affiliated Center Hospital of Shenyang Medical College, Shenyang, P. R. China.

Laboratory of Microbiology, School of Basic Medical Science, Shenyang Medical College, Shenyang, P. R. China.

出版信息

Nutr Cancer. 2021;73(8):1489-1497. doi: 10.1080/01635581.2020.1802494. Epub 2020 Aug 6.

Abstract

Cancer stem cell theory has been proposed to explain tumor heterogeneity and the carcinogenesis process. Highly tumorigenic lung cancer stem cells develop resistance to cisplatin (CDDP), a common chemotherapy drug. Herein, we attempted to clarify whether apigenin (API) can improve the antitumor efficiency of CDDP in lung cancer using cancer stem cells. Lung cancer stem cells were identified as CD 133 positive cancer cells in non-small cell lung cancer (NSCLC) A549, H1299 cells and CDDP-resistant NSCLC A549R cells. The cytotoxic effect of API was measured in CDDP-treated A549, H1299, and A549R cells. API repressed CD 133 positive cells and enhanced the antitumor effect of CDDP in A549, H1299, and A549R cells. The synergistic antitumor effect of API and CDDP was blocked by addition of the p53 inhibitor Pifithrin-α, and siRNA targeting the gene in A549R cells. Furthermore, API eliminates CDDP-induced CSC via p53, since A549R cells lacking p53 and Pifithrin-α addition derepressed the decrease in CD 133 positive cells after API treatment in CDDP-treated A549 and A549R cells. The findings indicate that API might eliminate cancer stem cells and enhance the antitumor effects of CDDP in NSCLC via p53.

摘要

癌症干细胞理论被提出以解释肿瘤异质性和致癌过程。高度致瘤性肺癌干细胞对顺铂(CDDP)这种常见的化疗药物产生耐药性。在此,我们试图通过癌症干细胞来阐明芹菜素(API)是否可以提高 CDDP 在肺癌中的抗肿瘤效率。肺癌干细胞被鉴定为非小细胞肺癌(NSCLC)A549、H1299 细胞和 CDDP 耐药性 NSCLC A549R 细胞中的 CD133 阳性癌细胞。API 在 CDDP 处理的 A549、H1299 和 A549R 细胞中测量细胞毒性作用。API 抑制 CD133 阳性细胞,并增强 A549、H1299 和 A549R 细胞中 CDDP 的抗肿瘤作用。API 和 CDDP 的协同抗肿瘤作用被添加 p53 抑制剂 Pifithrin-α和 A549R 细胞中针对基因的 siRNA 阻断。此外,API 通过 p53 消除 CDDP 诱导的 CSC,因为缺乏 p53 的 A549R 细胞和添加 Pifithrin-α 后,在 CDDP 处理的 A549 和 A549R 细胞中,API 处理后 CD133 阳性细胞的减少被去抑制。这些发现表明,API 可能通过 p53 消除肺癌干细胞并增强 NSCLC 中 CDDP 的抗肿瘤作用。

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