| Literature DB >> 31985119 |
Xiao-Zhong Liao1,2, Ying Gao2, Ling-Ling Sun1, Jia-Hui Liu2, Han-Rui Chen1, Ling Yu1, Zhuang-Zhong Chen1, Wen-Hui Chen3, Li-Zhu Lin1.
Abstract
Cisplatin (DDP) is one of the first-line chemotherapeutic agents for non-small cell lung cancer (NSCLC). However, repeated use of cisplatin in clinical practice often induces chemoresistance. The aims of this study were to investigate whether rosmarinic acid (RA) could reverse multidrug resistance (MDR) in NSCLC and to explore the underlying mechanisms. Our data demonstrated that RA significantly inhibited NSCLC cell proliferation and cell colony formation in a dose-dependent manner, induced G1 phase cell cycle arrest and apoptosis, and increased the sensitivity of cell lines resistant to DDP. Mechanistically, RA inhibited NSCLC cell growth, arrested cell cycle, and induced apoptosis by activating MAPK and inhibiting the expression of P-gp and MDR1, which correspondingly enhanced p21 and p53 expression. We observed that the growth of xenograft tumors derived from NSCLC cell lines in nude mice was significantly inhibited by combination therapy. We demonstrate that RA is a potentially effective MDR reversal agent for NSCLC, based on downregulation of MDR1 mRNA expression and P-gp. Together, these results emphasize the putative role of RA as a resistance reversal agent in NSCLC.Entities:
Keywords: MAPK; cisplatin; multidrug resistance; non-small cell lung cancer; rosmarinic acid
Year: 2020 PMID: 31985119 DOI: 10.1002/ptr.6584
Source DB: PubMed Journal: Phytother Res ISSN: 0951-418X Impact factor: 5.878