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虫草素通过下调癌症干细胞样特性增强吉西他滨对胆管癌的治疗潜力。

Cordycepin Enhanced Therapeutic Potential of Gemcitabine against Cholangiocarcinoma via Downregulating Cancer Stem-Like Properties.

作者信息

Lee Hong Kyu, Na Yun-Jung, Seong Su-Min, Ahn Dohee, Choi Kyung-Chul

机构信息

Laboratory of Biochemistry and Immunology, College of Veterinary Medicine, Chungbuk National University, Cheongju 28644, Republic of Korea.

出版信息

Biomol Ther (Seoul). 2024 May 1;32(3):369-378. doi: 10.4062/biomolther.2023.198. Epub 2024 Apr 9.

Abstract

Cordycepin, a valuable bioactive component isolated from , has been reported to possess anti-cancer potential and the property to enhance the effects of chemotherapeutic agents in various types of cancers. However, the ability of cordycepin to chemosensitize cholangiocarcinoma (CCA) cells to gemcitabine has not yet been evaluated. The current study was performed to evaluate the above, and the mechanisms associated with it. The study analyzed the effects of cordycepin in combination with gemcitabine on the cancer stem-like properties of the CCA SNU478 cell line, including its anti-apoptotic, migratory, and antioxidant effects. In addition, the combination of cordycepin and gemcitabine was evaluated in the CCA xenograft model. The cordycepin treatment significantly decreased SNU478 cell viability and, in combination with gemcitabine, additively reduced cell viability. The cordycepin and gemcitabine co-treatment significantly increased the Annexin V+ population and downregulated B-cell lymphoma 2 (Bcl-2) expression, suggesting that the decreased cell viability in the cordycepin+gemcitabine group may result from an increase in apoptotic death. In addition, the cordycepin and gemcitabine co-treatment significantly reduced the migratory ability of SNU478 cells in the wound healing and trans-well migration assays. It was observed that the cordycepin and gemcitabine cotreatment reduced the CD44CD133 population in SNU478 cells and the expression level of sex determining region Y-box 2 (Sox-2), indicating the downregulation of the cancer stem-like population. Cordycepin also enhanced oxidative damage mediated by gemcitabine in MitoSOX staining associated with the upregulated Kelch like ECH Associated Protein 1 (Keap1)/nuclear factor erythroid 2-related factor 2 (Nrf2) expression ratio. In the SNU478 xenograft model, co-administration of cordycepin and gemcitabine additively delayed tumor growth. These results indicate that cordycepin potentiates the chemotherapeutic property of gemcitabine against CCA, which results from the downregulation of its cancer-stem-like properties. Hence, the combination therapy of cordycepin and gemcitabine may be a promising therapeutic strategy in the treatment of CCA.

摘要

虫草素是从[来源未提及]中分离出的一种有价值的生物活性成分,据报道具有抗癌潜力,并能增强化疗药物对各种癌症的治疗效果。然而,虫草素使胆管癌细胞(CCA)对吉西他滨产生化疗增敏作用的能力尚未得到评估。本研究旨在评估上述作用及其相关机制。该研究分析了虫草素与吉西他滨联合使用对CCA SNU478细胞系癌症干细胞样特性的影响,包括其抗凋亡、迁移和抗氧化作用。此外,还在CCA异种移植模型中评估了虫草素与吉西他滨的联合作用。虫草素处理显著降低了SNU478细胞的活力,与吉西他滨联合使用时,可进一步降低细胞活力。虫草素与吉西他滨联合处理显著增加了膜联蛋白V阳性细胞群体,并下调了B细胞淋巴瘤2(Bcl-2)的表达,这表明虫草素+吉西他滨组细胞活力的降低可能是由于凋亡死亡增加所致。此外,在伤口愈合和Transwell迁移试验中,虫草素与吉西他滨联合处理显著降低了SNU478细胞的迁移能力。观察到虫草素与吉西他滨联合处理降低了SNU478细胞中CD44+CD133+细胞群体以及性别决定区Y盒2(Sox-2)的表达水平,表明癌症干细胞样群体的下调。虫草素还增强了吉西他滨介导的线粒体超氧化物染色中的氧化损伤,这与Kelch样ECH相关蛋白1(Keap1)/核因子红细胞2相关因子2(Nrf2)表达比值上调有关。在SNU478异种移植模型中,虫草素与吉西他滨联合给药可进一步延迟肿瘤生长。这些结果表明,虫草素增强了吉西他滨对CCA的化疗作用,这是由于其癌症干细胞样特性的下调所致。因此,虫草素与吉西他滨的联合治疗可能是治疗CCA的一种有前景的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b090/11063483/f55a419971b8/bt-32-3-368-f1.jpg

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