Di Giacomo Silvia, Gullì Marco, Facchinetti Roberta, Minacori Marco, Mancinelli Romina, Percaccio Ester, Scuderi Caterina, Eufemi Margherita, Di Sotto Antonella
Department of Physiology and Pharmacology "V. Erspamer", Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome, Italy.
Department of Biochemical Science "A. Rossi Fanelli", Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome, Italy.
Pharmaceutics. 2022 Jun 14;14(6):1264. doi: 10.3390/pharmaceutics14061264.
A combination of anticancer drugs and chemosensitizing agents has been approached as a promising strategy to potentiate chemotherapy and reduce toxicity in aggressive and chemoresistant cancers, like hepatocellular carcinoma (HCC), cholangiocarcinoma (CCA), and pancreatic ductal adenocarcinoma (PDAC). In the present study, the ability of caryophyllane sesquiterpenes to potentiate sorafenib efficacy was studied in HCC, CCA, and PDAC cell models, focusing on the modulation of STAT3 signaling and ABC transporters; tolerability studies in normal cells were also performed. Results showed that the combination of sorafenib and caryophyllane sesquiterpenes synergized the anticancer drug, especially in pancreatic Bx-PC3 adenocarcinoma cells; a similar trend, although with lower efficacy, was found for the standard ABC transporter inhibitors. Synergistic effects were associated with a modulation of MDR1 (or Pgp) and MRP transporters, both at gene and protein level; moreover, activation of STAT3 cascade and cell migration appeared significantly affected, suggesting that the STAT3/ABC-transporters axis finely regulated efficacy and chemoresistance to sorafenib, thus appearing as a suitable target to overcome drawbacks of sorafenib-based chemotherapy in hepato-biliary-pancreatic cancers. Present findings strengthen the interest in caryophyllane sesquiterpenes as chemosensitizing and chemopreventive agents and contribute to clarifying drug resistance mechanisms in HCC, CCA, and PDAC cancers and to developing possible novel therapeutic strategies.
将抗癌药物与化学增敏剂联合使用,已被视为一种有前景的策略,可增强化疗效果,并降低侵袭性和化疗耐药性癌症(如肝细胞癌(HCC)、胆管癌(CCA)和胰腺导管腺癌(PDAC))的毒性。在本研究中,在HCC、CCA和PDAC细胞模型中研究了石竹烯倍半萜增强索拉非尼疗效的能力,重点关注STAT3信号传导和ABC转运蛋白的调节;还对正常细胞进行了耐受性研究。结果表明,索拉非尼与石竹烯倍半萜联合使用可增强抗癌药物的效果,尤其是在胰腺Bx-PC3腺癌细胞中;对于标准ABC转运蛋白抑制剂,也发现了类似趋势,尽管效果较低。协同效应与MDR1(或Pgp)和MRP转运蛋白在基因和蛋白质水平的调节有关;此外,STAT3级联反应的激活和细胞迁移也受到显著影响,这表明STAT3/ABC转运蛋白轴精细调节了对索拉非尼的疗效和化疗耐药性,因此似乎是克服肝胆胰癌中基于索拉非尼化疗缺点的合适靶点。目前的研究结果增强了人们对石竹烯倍半萜作为化学增敏剂和化学预防剂的兴趣,并有助于阐明HCC、CCA和PDAC癌症中的耐药机制,以及开发可能的新型治疗策略。