| Literature DB >> 32124474 |
Xiaomei Tao1,2,3, Yefeng Yin1, Dongbo Lian1, Hongyan Gu1, Wen Chen4, Lu Yang1, Gang Yin1, Pengfei Liu1, Lili Li1, Yuanyuan Wei1, Zhengzheng Xie1, Fei Liu5, Hangshuo Sui6, Dan Yan1,2,3, Weiwei Tao7.
Abstract
Cancer stem cells have been identified as the major cause of cancer initiation and progression. To investigate the effects of puerarin 6″-O-xyloside (PXY), derived from Pueraria lobata (Willd.) Ohwi, on lung cancer stem cells, we enriched and identified a subpopulation of lung cancer stem-like cells (LCSLCs) derived from lung adenocarcinoma A549 cells with traits including high self-renewal and invasive capability in vitro, elevated tumourigenicity in vivo, and high expression of stem cell markers CD44, CD133 and aldehyde dehydrogenase 1 (ALDH1). We found that PXY could impair cell viability, suppress self-renewal and invasive capability, and decrease CD133, CD44 and ALDH1 mRNA expression in LCSLCs in a dose-dependent manner. Furthermore, we showed that PXY suppressed the self-renewal and invasive capability of LCSLCs at least in part through suppressing the activation of Akt/c-Myc signalling. In conclusion, PXY can block the traits of LCSLCs, indicating that PXY may be a candidate compound for lung adenocarcinoma therapy via eliminating LCSLCs.Entities:
Keywords: Akt/c-Myc signalling; Puerarin 6″-O-xyloside; cell invasion; lung cancer stem-like cells; self-renewal
Year: 2020 PMID: 32124474 DOI: 10.1111/1440-1681.13294
Source DB: PubMed Journal: Clin Exp Pharmacol Physiol ISSN: 0305-1870 Impact factor: 2.557