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姜黄素通过增加 ROS 和细胞周期停滞逆转 NNMT 诱导的结直肠癌细胞对 5-氟尿嘧啶的耐药性。

Curcumin Reverses NNMT-Induced 5-Fluorouracil Resistance via Increasing ROS and Cell Cycle Arrest in Colorectal Cancer Cells.

机构信息

Department of Clinical Laboratory, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou 310016, China.

Key Laboratory of Precision Medicine in Diagnosis and Monitoring Research of Zhejiang Province, Hangzhou 310016, China.

出版信息

Biomolecules. 2021 Aug 31;11(9):1295. doi: 10.3390/biom11091295.

Abstract

Nicotinamide -methyltransferase (NNMT) plays multiple roles in improving the aggressiveness of colorectal cancer (CRC) and enhancing resistance to 5-Fluorouracil (5-FU), making it an attractive therapeutic target. Curcumin (Cur) is a promising natural compound, exhibiting multiple antitumor effects and potentiating the effect of 5-FU. The aim of the present study is to explore the effect of Cur on attenuating NNMT-induced resistance to 5-FU in CRC. A panel of CRC cell lines with different NNMT expressions are used to characterize the effect of Cur. Herein, it is observed that Cur can depress the expression of NNMT and p-STAT3 in CRC cells. Furthermore, Cur can induce inhibition of cell proliferation, G2/M phase cell cycle arrest, and reactive oxygen species (ROS) generation, especially in high-NNMT-expression CRC cell lines. Cur can also re-sensitize high-NNMT-expression CRC cells to 5-FU both in vitro and in vivo. In summary, it is proposed that Cur can reverse NNMT-induced cell proliferation and 5-FU resistance through ROS generation and cell cycle arrest. Given that Cur has long been used, we suppose that Cur is a promising anticancer drug candidate with minimal side effects for human CRC therapy and can attenuate NNMT-induced resistance to 5-FU.

摘要

烟酰胺 -N- 甲基转移酶(NNMT)在提高结直肠癌(CRC)的侵袭性和增强对 5-氟尿嘧啶(5-FU)的耐药性方面发挥多种作用,使其成为有吸引力的治疗靶点。姜黄素(Cur)是一种很有前途的天然化合物,具有多种抗肿瘤作用,并增强 5-FU 的作用。本研究旨在探讨姜黄素对减轻 NNMT 诱导的 CRC 对 5-FU 耐药性的影响。使用一组具有不同 NNMT 表达的 CRC 细胞系来表征 Cur 的作用。在此,观察到 Cur 可以下调 CRC 细胞中 NNMT 和 p-STAT3 的表达。此外,Cur 可以诱导细胞增殖抑制、G2/M 期细胞周期阻滞和活性氧(ROS)生成,尤其是在高 NNMT 表达的 CRC 细胞系中。Cur 还可以在体外和体内重新使高 NNMT 表达的 CRC 细胞对 5-FU 敏感。总之,提出 Cur 可以通过 ROS 生成和细胞周期阻滞来逆转 NNMT 诱导的细胞增殖和 5-FU 耐药性。鉴于 Cur 长期以来一直被使用,我们假设 Cur 是一种很有前途的抗癌药物候选物,对人类 CRC 治疗的副作用最小,可以减轻 NNMT 诱导的对 5-FU 的耐药性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d366/8470329/b8188001b2d8/biomolecules-11-01295-g0A1.jpg

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