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姜黄素在增敏顺铂对非小细胞肺癌细胞系来源的肿瘤干细胞样细胞群的作用中的协同作用。

Synergistic Roles of Curcumin in Sensitising the Cisplatin Effect on a Cancer Stem Cell-Like Population Derived from Non-Small Cell Lung Cancer Cell Lines.

机构信息

Lung Stem Cell and Gene Therapy Group, Regenerative Medicine Cluster, Advanced Medical and Dental Institute (IPPT), Universiti Sains Malaysia, Sains@Bertam Kepala Batas, Penang 13200, Malaysia.

Analytical Biochemistry Research Centre (ABrC), Universiti Sains Malaysia, Penang 11800, Malaysia.

出版信息

Molecules. 2021 Feb 18;26(4):1056. doi: 10.3390/molecules26041056.

DOI:10.3390/molecules26041056
PMID:33670440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7922800/
Abstract

Cancer stem cells (CSCs) represent a small subpopulation within a tumour. These cells possess stem cell-like properties but also initiate resistance to cytotoxic agents, which contributes to cancer relapse. Natural compounds such as curcumin that contain high amounts of polyphenols can have a chemosensitivity effect that sensitises CSCs to cytotoxic agents such as cisplatin. This study was designed to investigate the efficacy of curcumin as a chemo-sensitiser in CSCs subpopulation of non-small cell lung cancer (NSCLC) using the lung cancer adenocarcinoma human alveolar basal epithelial cells A549 and H2170. The ability of curcumin to sensitise lung CSCs to cisplatin was determined by evaluating stemness characteristics, including proliferation activity, colony formation, and spheroid formation of cells treated with curcumin alone, cisplatin alone, or the combination of both at 24, 48, and 72 h. The mRNA level of genes involved in stemness was analysed using quantitative real-time polymerase chain reaction. Liquid chromatography-mass spectrometry was used to evaluate the effect of curcumin on the CSC niche. A combined treatment of A549 subpopulations with curcumin reduced cellular proliferation activity at all time points. Curcumin significantly ( < 0.001) suppressed colonies formation by 50% and shrank the spheroids in CSC subpopulations, indicating inhibition of their self-renewal capability. This effect also was manifested by the down-regulation of , , and . Curcumin also regulated the niche of CSCs by inhibiting chemoresistance proteins, aldehyde dehydrogenase, metastasis, angiogenesis, and proliferation of cancer-related proteins. These results show the potential of using curcumin as a therapeutic approach for targeting CSC subpopulations in non-small cell lung cancer.

摘要

癌症干细胞(CSC)是肿瘤中的一小部分亚群。这些细胞具有干细胞样特性,但也会引发对细胞毒性药物的耐药性,从而导致癌症复发。含有大量多酚的天然化合物如姜黄素可以产生化疗增敏作用,使 CSC 对顺铂等细胞毒性药物敏感。本研究旨在使用肺癌腺癌人肺泡基底上皮细胞 A549 和 H2170 研究姜黄素作为非小细胞肺癌(NSCLC)CSC 亚群的化疗增敏剂的功效。通过评估单独用姜黄素、顺铂或两者联合处理细胞 24、48 和 72 小时后的干细胞特性,包括增殖活性、集落形成和球体形成,来确定姜黄素使肺 CSC 对顺铂敏感的能力。使用实时定量聚合酶链反应分析参与干细胞特性的基因的 mRNA 水平。使用液相色谱-质谱联用评估姜黄素对 CSC 生态位的影响。A549 亚群联合用姜黄素处理可降低所有时间点的细胞增殖活性。姜黄素显著(<0.001)抑制集落形成 50%,并缩小 CSC 亚群中的球体,表明其自我更新能力受到抑制。这种作用还表现为下调 、 和 。姜黄素还通过抑制化学抗性蛋白、醛脱氢酶、转移、血管生成和与癌症相关蛋白的增殖来调节 CSCs 的生态位。这些结果表明,使用姜黄素作为针对非小细胞肺癌 CSC 亚群的治疗方法具有潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/02ac4d31b778/molecules-26-01056-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/e459d8190a69/molecules-26-01056-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/7c61e8de1aca/molecules-26-01056-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/ecee725b1ae9/molecules-26-01056-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/2b7170d3f0eb/molecules-26-01056-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/3d1e916c2140/molecules-26-01056-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/02ac4d31b778/molecules-26-01056-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/e459d8190a69/molecules-26-01056-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/7c61e8de1aca/molecules-26-01056-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/ecee725b1ae9/molecules-26-01056-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/2b7170d3f0eb/molecules-26-01056-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/3d1e916c2140/molecules-26-01056-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4300/7922800/02ac4d31b778/molecules-26-01056-g006.jpg

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