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白花丹素通过增加人舌鳞癌细胞内 ROS 增强顺铂的抗癌疗效。

Plumbagin Enhances the Anticancer Efficacy of Cisplatin by Increasing Intracellular ROS in Human Tongue Squamous Cell Carcinoma.

机构信息

Department of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Nanchang University, Nanchang, 330006 Jiangxi, China.

Department of Pathology, The First Affiliated Hospital of Nanchang University, Nanchang, 330006 Jiangxi, China.

出版信息

Oxid Med Cell Longev. 2020 Mar 25;2020:5649174. doi: 10.1155/2020/5649174. eCollection 2020.

Abstract

Cisplatin is widely used in the treatment of tongue squamous cell carcinoma (TSCC), but its clinical efficacy is limited by drug resistance and toxic side effects. Hence, a novel compound capable of enhancing the anticancer effect of cisplatin while reducing the side effects is urgently needed. We have previously shown that plumbagin (PLB), an anticancer phytochemical, is able to inhibit the growth of TSCC and . The objective of this study was to investigate the effect of PLB in reversing the resistance of TSCC to cisplatin as well as its molecular mechanisms. Here, we found that PLB enhances cisplatin-induced cytotoxicity, apoptosis, and autophagy in CAL27 and cisplatin-resistant CAL27/CDDP cells. PLB could inhibit the viability and growth of TSCC cells by increasing the production of intracellular reactive oxygen species (ROS). In addition, the combination treatment of PLB and cisplatin resulted in a synergistic inhibition of TSCC viability, apoptosis, and autophagy by increasing intracellular ROS, which may be achieved by activating JNK and inhibiting AKT/mTOR signaling pathways. Finally, the synergistic treatment was also demonstrated . Therefore, PLB combined with cisplatin is a potential therapeutic strategy against therapy TSCC cisplatin resistance.

摘要

顺铂广泛用于治疗舌鳞状细胞癌(TSCC),但其临床疗效受到耐药性和毒副作用的限制。因此,迫切需要一种能够增强顺铂抗癌作用同时降低副作用的新型化合物。我们之前已经表明,抗癌植物化学物质白花丹素(PLB)能够抑制 TSCC 和 的生长。本研究的目的是探讨 PLB 逆转 TSCC 对顺铂耐药性的作用及其分子机制。在这里,我们发现 PLB 增强了 CAL27 和耐顺铂的 CAL27/CDDP 细胞中顺铂诱导的细胞毒性、细胞凋亡和自噬。PLB 可以通过增加细胞内活性氧物质(ROS)的产生来抑制 TSCC 细胞的活力和生长。此外,PLB 和顺铂的联合治疗通过增加细胞内 ROS 导致 TSCC 活力、凋亡和自噬的协同抑制,这可能通过激活 JNK 和抑制 AKT/mTOR 信号通路来实现。最后,还证明了协同治疗的效果。因此,PLB 联合顺铂是治疗 TSCC 顺铂耐药的一种有潜力的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d866/7136784/2c86c9e733f1/OMCL2020-5649174.001.jpg

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