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吉西他滨与甲硝唑联合使用是一种治疗胆管癌癌干细胞样肿瘤的有前景的治疗策略。

Combined Gemcitabine and Metronidazole Is a Promising Therapeutic Strategy for Cancer Stem-like Cholangiocarcinoma.

作者信息

Kawamoto Makoto, Umebayashi Masayo, Tanaka Hiroto, Koya Norihiro, Nakagawa Sinichiro, Kawabe Ken, Onishi Hideya, Nakamura Masafumi, Morisaki Takashi

机构信息

Department of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Anticancer Res. 2018 May;38(5):2739-2748. doi: 10.21873/anticanres.12516.

Abstract

BACKGROUND/AIM: Metronidazole (MNZ) is a common antibiotic that exerts disulfiram-like effects when taken together with alcohol. However, the relationship between MNZ and aldehyde dehydrogenase (ALDH) activity remains unclear. This study investigated whether MNZ reduces cancer stemness by suppressing ALDH activity and accordingly reducing the malignancy of cholangiocarcinoma (CCA).

MATERIALS AND METHODS

We developed gemcitabine (GEM)-resistant TFK-1 cells and originally established CCA cell line from a patient with GEM-resistant CCA. Using these cell lines, we analyzed the impacts of MNZ for cancer stem cell markers, invasiveness, and chemosensitivity.

RESULTS

MNZ reduced ALDH activity in GEM-resistant CCA cells, leading to decreased invasiveness and enhanced chemosensitivity. MNZ diminished the invasiveness by inducing mesenchymal-epithelial transition and enhancing chemosensitivity by increasing ENT1 (equilibrative nucleoside transporter 1) and reducing RRM1 (ribonucleotide reductase M1).

CONCLUSION

MNZ reduced cancer stemness in GEM-resistant CCA cells. Combined GEM and MNZ would be a promising therapeutic strategy for cancer stem-like CAA.

摘要

背景/目的:甲硝唑(MNZ)是一种常见抗生素,与酒精同时服用时会产生双硫仑样效应。然而,MNZ与醛脱氢酶(ALDH)活性之间的关系仍不清楚。本研究调查了MNZ是否通过抑制ALDH活性从而降低胆管癌(CCA)的恶性程度来减少癌症干性。

材料与方法

我们构建了吉西他滨(GEM)耐药的TFK-1细胞,并从一名GEM耐药CCA患者中最初建立了CCA细胞系。使用这些细胞系,我们分析了MNZ对癌症干细胞标志物、侵袭性和化疗敏感性的影响。

结果

MNZ降低了GEM耐药CCA细胞中的ALDH活性,导致侵袭性降低和化疗敏感性增强。MNZ通过诱导间充质-上皮转化降低侵袭性,并通过增加ENT1(平衡核苷转运体1)和降低RRM1(核糖核苷酸还原酶M1)增强化疗敏感性。

结论

MNZ降低了GEM耐药CCA细胞中的癌症干性。联合使用GEM和MNZ可能是治疗癌症干细胞样CAA的一种有前景的治疗策略。

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