Xu Yafei, Kong Weimiao, Zhao Simin, Xiong Dan, Wang Yejun
Department of Cell Biology and Genetics, Shenzhen University Health Science Center, 1066 Xue Yuan Road, Xili, Nanshan District, Shenzhen, Guangdong 518060, China.
Youth Innovation Team of Medical Bioinformatics, Shenzhen University Health Science Center, 1066 Xue Yuan Road, Xili, Nanshan District, Shenzhen, Guangdong 518060, China.
Carcinogenesis. 2024 Aug 12;45(8):556-568. doi: 10.1093/carcin/bgae032.
Cisplatin (DDP)-based combined chemotherapy or concurrent chemoradiotherapy is the mainstay treatment for advanced-stage nasopharyngeal carcinoma (NPC), but needs improvement due to its severe side effects. Capsaicin (CAP) can enhance the anti-tumor activity of cytotoxic drugs. The aim of this study was to investigate the anti-metastasis activity of CAP in combination with DDP in NPC. Herein, CAP and DDP showed synergistic cytotoxic effects on NPC cells. CAP alone and DDP alone inhibited NPC migration and invasion in vitro and in vivo, and the combination of CAP and DDP had the greatest effect. Moreover, CAP upregulated the mRNA and protein expressions of serpin family B member 2 (SERPINB2). Further results showed that both SERPINB2 mRNA and protein expressions were downregulated in NPC cell lines and tissues and SERPINB2 overexpression inhibited NPC migration and invasion in vitro and in vivo, while silencing SERPINB2 acted oppositely. In addition, SERPINB2 was abnormally expressed in head and neck squamous cell carcinoma and other multiple cancers, and downregulation of SERPINB2 predicted poor prognosis in head and neck squamous cell carcinoma according to the Cancer Genome Atlas database. We further found that SERPINB2 overexpression inhibited epithelial-mesenchymal transition (EMT) and the phosphorylated extracellular signal-regulated kinase (p-ERK), and the inhibitory effect was enhanced by CAP and DDP. Altogether, our results suggest that the combined inhibition of CAP and DDP on NPC metastasis may be related to the inhibition of epithelial-mesenchymal transition and ERK signals mediated by SERPINB2, and CAP may help to improve the efficacy of DDP in the treatment of NPC and develop new therapeutic approaches.
以顺铂(DDP)为基础的联合化疗或同步放化疗是晚期鼻咽癌(NPC)的主要治疗方法,但由于其严重的副作用而需要改进。辣椒素(CAP)可增强细胞毒性药物的抗肿瘤活性。本研究的目的是探讨CAP联合DDP对鼻咽癌的抗转移活性。在此,CAP和DDP对NPC细胞显示出协同细胞毒性作用。单独使用CAP和单独使用DDP在体外和体内均抑制NPC的迁移和侵袭,且CAP与DDP联合使用效果最佳。此外,CAP上调了丝氨酸蛋白酶抑制剂家族B成员2(SERPINB2)的mRNA和蛋白表达。进一步的结果表明,SERPINB2的mRNA和蛋白表达在NPC细胞系和组织中均下调,SERPINB2的过表达在体外和体内均抑制NPC的迁移和侵袭,而沉默SERPINB2则起相反作用。此外,SERPINB2在头颈部鳞状细胞癌和其他多种癌症中异常表达,根据癌症基因组图谱数据库,SERPINB2的下调预示着头颈部鳞状细胞癌的预后不良。我们进一步发现,SERPINB2的过表达抑制上皮-间质转化(EMT)和磷酸化细胞外信号调节激酶(p-ERK),且CAP和DDP可增强这种抑制作用。总之,我们的结果表明,CAP和DDP联合抑制NPC转移可能与抑制由SERPINB2介导的上皮-间质转化和ERK信号有关,且CAP可能有助于提高DDP治疗NPC的疗效并开发新的治疗方法。
Cancer Commun (Lond). 2018-5-3
Biochim Biophys Acta Mol Basis Dis. 2024-10