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作 者:汪润坤 金燕(综述) 许斌(审校)[2] WANG Runkun;JIN Yan;XU Bin(Department of Oncology,No.1 People Hospital of Guangshui,Suizhou Hubei 432700;Cancer Center,Renmin Hospital of Wuhan University,Wuhan 430060,China)
机构地区:[1]广水市第一人民医院肿瘤科,湖北随州432700 [2]武汉大学人民医院肿瘤中心,武汉430060
出 处:《临床与病理杂志》2022年第5期1239-1246,共8页Journal of Clinical and Pathological Research
摘 要:临床上肿瘤患者在接受化疗和靶向治疗后体内形成耐药的肿瘤细胞。这类细胞具有增殖缓慢、细胞代谢调节性强、表型可塑性高和对肿瘤微环境的适应性强等特征。这些特征背后的分子机制与肿瘤细胞产生耐药相关。耐药细胞的减速机制可以发生在细胞内,也可以通过微环境介导。耐药细胞可以通过线粒体呼吸,调控蛋白质合成,和增强抗氧化途径的方式来调节细胞代谢。耐药细胞通过上皮间质转化和转分化来改变细胞表型。耐药细胞通过和肿瘤微环境中的肿瘤相关巨噬细胞、肿瘤相关成纤维细胞等其他细胞相互作用,增强其对微环境的适应能力。结合临床现状,开发可靠的临床前肿瘤耐药细胞模型对进一步研究肿瘤耐药细胞的特性和寻找临床治疗新策略具有重要意义。Cancer patients with receiving chemotherapy and targeted therapy have persistent cancer cells remaining in their bodies.These cells are labelled by their slow proliferation,high metabolic plasticity,high phenotypic plasticity,and strong adaptability to the tumor microenvironment.The molecular mechanisms of these characteristics promote the development of drug resistance in persistent cancer cells.The slow proliferation mechanism of persistent cancer cells can occur intracellularly or be triggered by microenvironment.Cell metabolism is regulated by mitochondrial respiration,protein synthesis,and antioxidant pathways in persistent cancer cells.The phenotype of persistent cancer cells is changed by epithelial-to-mesenchymal transition and transdifferentiation.Tumorassociated macrophages,cancer-associated fibroblasts and other cells in the microenvironment interact with persistent cancer cells to enhance their adaptability to the microenvironment.At the present clinical situation,the development of a reliable preclinical cancer models is of great significance to further study the characteristics of persistent cancer cells so that new clinical strategies targeting persistent cancer cells for doctors to carry out.
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