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首页> 外文期刊>Integrative cancer therapies. >Effects of Withania somnifera and Tinospora cordifolia Extracts on the Side Population Phenotype of Human Epithelial Cancer Cells
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Effects of Withania somnifera and Tinospora cordifolia Extracts on the Side Population Phenotype of Human Epithelial Cancer Cells

机译:茄子和茄子提取物对人上皮癌细胞侧群表型的影响

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Recent reports suggest the existence of a subpopulation of stem-like cancer cells, termed as cancer stem cells (CSCs), which bear functional and phenotypic resemblance with the adult, tissue-resident stem cells. Side population (SP) assay based on differential efflux of Hoechst 33342 has been effectively used for the isolation of CSCs. The drug resistance properties of SP cells are typically due to the increased expression of ABC transporters leading to drug efflux. Conventionally used chemotherapeutic drugs may often leads to an enrichment of SP, revealing their inability to target the drug-resistant SP and CSCs. Thus, identification of agents that can reduce the SP phenotype is currently in vogue in cancer therapeutics. Withania somnifera (WS) and Tinospora cordifolia (TC) have been used in Ayurveda for treating various diseases, including cancer. In the current study, we have investigated the effects of ethanolic (ET) extracts of WS and TC on the cancer SP phenotype. Interestingly, we found significant decrease in SP on treatment with TC-ET, but not with WS-ET. The SP-inhibitory TC-ET was further fractionated into petroleum ether (TC-PET), dichloromethane (TC-DCM), and n-butyl alcohol (TC-nBT) fractions using bioactivity-guided fractionation. Our data revealed that TC-PET and TC-DCM, but not TC-nBT, significantly inhibited SP in a dose-dependent manner. Furthermore, flow cytometry–based functional assays revealed that TC-PET and TC-DCM significantly inhibited ABC-B1 and ABC-G2 transporters and sensitized cancer cells toward chemotherapeutic drug-mediated cytotoxicity. Thus, the TC-PET and TC-DCM may harbor phytochemicals with the potential to reverse the drug-resistant phenotype, thus improving the efficacy of cancer chemotherapy.
机译:最近的报道表明,存在着干细胞样癌细胞的亚群,称为癌症干细胞(CSCs),其功能和表型与成年的组织驻留干细胞相似。基于Hoechst 33342差分流出的侧群(SP)分析已有效地用于分离CSC。 SP细胞的耐药性通常是由于ABC转运蛋白表达增加导致药物外排。常规使用的化学治疗药物可能经常导致SP的富集,这表明它们无法靶向耐药SP和CSC。因此,目前可以在癌症治疗剂中鉴定可以降低SP表型的药物。在印度草医学中,Withania somnifera(WS)和Tinospora cordifolia(TC)已用于治疗各种疾病,包括癌症。在当前的研究中,我们已经研究了WS和TC的乙醇(ET)提取物对癌症SP表型的影响。有趣的是,我们发现用TC-ET而非SP-WS-ET可以显着降低SP。抑制SP的TC-ET使用生物活性指导分馏进一步分为石油醚(TC-PET),二氯甲烷(TC-DCM)和正丁醇(TC-nBT)馏分。我们的数据显示,TC-PET和TC-DCM而非TC-nBT以剂量依赖性方式显着抑制SP。此外,基于流式细胞仪的功能分析表明,TC-PET和TC-DCM显着抑制ABC-B1和ABC-G2转运蛋白,并使癌细胞对化疗药物介导的细胞毒性敏感。因此,TC-PET和TC-DCM可能包含具有逆转耐药表型潜力的植物化学物质,从而提高了癌症化学疗法的功效。

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