...
首页> 外文期刊>Molecules >Chelerythrine Chloride Downregulates β-Catenin and Inhibits Stem Cell Properties of Non-Small Cell Lung Carcinoma
【24h】

Chelerythrine Chloride Downregulates β-Catenin and Inhibits Stem Cell Properties of Non-Small Cell Lung Carcinoma

机译:Chererythrine氯化物下调β-catenin并抑制非小细胞肺癌的干细胞性能

获取原文
           

摘要

Plant secondary metabolites have been seen as alternatives to seeking new medicines for treating various diseases. Phytochemical scientists remain hopeful that compounds isolated from natural sources could help alleviate the leading problem in oncology—the lung malignancy that kills an estimated two million people annually. In the present study, we characterized a medicinal compound benzophenanthridine alkaloid, called chelerythrine chloride for its anti-tumorigenic activities. Cell viability assays confirmed its cytotoxicity and anti-proliferative activity in non-small cell lung carcinoma (NSCLC) cell lines. Immunofluorescence staining of β-catenin revealed that there was a reduction of nuclear content as well as overall cellular content of β-catenin after treating NCI-H1703 with chelerythrine chloride. In functional characterizations, we observed favorable inhibitory activities of chelerythrine chloride in cancer stem cell (CSC) properties, which include soft agar colony-forming, migration, invasion, and spheroid forming abilities. Interesting observations in chelerythrine chloride treatment noted that its action abides to certain concentration-specific-targeting behavior in modulating β-catenin expression and apoptotic cell death. The downregulation of β-catenin implicates the downregulation of CSC transcription factors like SOX2 and MYC. In conclusion, chelerythrine chloride has the potential to mitigate cancer growth due to inhibitory actions toward the tumorigenic activity of CSC in lung cancer and it can be flexibly adjusted according to concentration to modulate specific targeting in different cell lines.
机译:植物次生代谢产物被视为寻求治疗各种疾病的新药的替代品。植物化学科学家仍然希望从自然来源中分离的化合物可以帮助缓解肿瘤学中的主要问题 - 肺部恶性肿瘤每年损失估计的200万人。在本研究中,我们以抗致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致致荷的活性的药物化合物苯并苯蒽醌生物碱。细胞活力测定证实了非小细胞肺癌(NSCLC)细胞系中的其细胞毒性和抗增殖活性。 β-catenin的免疫荧光染色表明,在用Chelerythrine氯化物处理NCI-H1703后,核含量和β-catenin的总细胞含量降低。在功能性表征中,我们观察到癌症干细胞(CSC)性质中的Chelerythrine氯化物的有利抑制活性,包括软琼脂形成,迁移,侵袭和球状形成能力。在Chelerythrine氯化物处理中的有趣观察指出,其作用在调节β-catenin表达和凋亡细胞死亡中均致力于某些浓度特异性靶向行为。 β-catenin的下调意味着Sox2和Myc等CSC转录因子的下调。总之,十三萜氯化物具有减轻由于肺癌中CSC致致致致致瘤活性的抑制作用而减轻癌症生长,并且可以根据浓度灵活地调整以调节不同细胞系中的特异性靶向。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号