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二甲双胍增强5-氟尿嘧啶和奥沙利铂对结肠癌细胞及裸鼠的治疗效果。

Metformin Enhancement of Therapeutic Effects of 5-Fluorouracil and Oxaliplatin in Colon Cancer Cells and Nude Mice.

作者信息

Yip Kwan-Ling, Tsai Tsen-Ni, Yang I-Ping, Miao Zhi-Feng, Chen Yen-Cheng, Li Ching-Chun, Su Wei-Chih, Chang Tsung-Kun, Huang Ching-Wen, Tsai Hsiang-Lin, Yeh Yung-Sung, Wang Jaw-Yuan

机构信息

Division of Colorectal Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.

Department of Nursing, Shu-Zen College of Medicine and Management, Kaohsiung 82144, Taiwan.

出版信息

Biomedicines. 2022 Apr 20;10(5):955. doi: 10.3390/biomedicines10050955.

Abstract

Studies have demonstrated that metformin has antitumor effects in addition to therapeutic effects on hyperglycemia; however, few studies have explored the effects of metformin in chemotherapy. Therefore, we hypothesized that the administration of metformin would enhance the therapeutic effects of 5-fluorouracil and oxaliplatin (FuOx) to inhibit the growth of colorectal cancer (CRC) cells in vitro and in vivo. The results of our in vitro experiments demonstrated that metformin significantly increased the effects of FuOx with respect to cell proliferation (p < 0.05), colony formation (p < 0.05), and migration (p < 0.01) and induced cell cycle arrest in the G0/G1 phase in HT29 cells and the S phase in SW480 and SW620 cells (p < 0.05). Flow cytometry analysis revealed that metformin combined with FuOx induced late apoptosis (p < 0.05) by mediating mitochondria-related Mcl-1 and Bim protein expression. Furthermore, in vivo, metformin combined with FuOx more notably reduced tumor volume than FuOx or metformin alone did in BALB/c mice (p < 0.05). These findings demonstrate that metformin may act as an adjunctive agent to enhance the chemosensitivity of CRC cells to FuOx. However, further clinical trials are warranted to validate the clinical implications of the findings.

摘要

研究表明,二甲双胍除了对高血糖有治疗作用外,还具有抗肿瘤作用;然而,很少有研究探讨二甲双胍在化疗中的作用。因此,我们假设给予二甲双胍会增强5-氟尿嘧啶和奥沙利铂(FuOx)的治疗效果,从而在体外和体内抑制结直肠癌(CRC)细胞的生长。我们的体外实验结果表明,二甲双胍在细胞增殖(p < 0.05)、集落形成(p < 0.05)和迁移(p < 0.01)方面显著增强了FuOx的作用,并使HT29细胞的细胞周期停滞在G0/G1期,使SW480和SW620细胞的细胞周期停滞在S期(p < 0.05)。流式细胞术分析显示,二甲双胍与FuOx联合使用通过介导与线粒体相关的Mcl-1和Bim蛋白表达诱导晚期凋亡(p < 0.05)。此外,在体内,二甲双胍与FuOx联合使用比单独使用FuOx或二甲双胍更显著地减小了BALB/c小鼠的肿瘤体积(p < 0.05)。这些发现表明,二甲双胍可能作为一种辅助药物来增强CRC细胞对FuOx的化疗敏感性。然而,需要进一步的临床试验来验证这些发现的临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e68f/9138369/49a1bc632eba/biomedicines-10-00955-g001.jpg

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