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In vitro and in vivo antiproliferative activity of metformin on stem-like cells isolated from spontaneous canine mammary carcinomas: translational implications for human tumors

机译:二甲双胍对自发性自发性乳腺癌分离的干样细胞的体外和体内抗增殖活性:对人类肿瘤的翻译意义

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摘要

BackgroundCancer stem cells (CSCs) are considered the cell subpopulation responsible for breast cancer (BC) initiation, growth, and relapse. CSCs are identified as self-renewing and tumor-initiating cells, conferring resistance to chemo- and radio-therapy to several neoplasias. Nowadays, th (about 10mM)e pharmacological targeting of CSCs is considered an ineludible therapeutic goal. The antidiabetic drug metformin was reported to suppress in vitro and in vivo CSC survival in different tumors and, in particular, in BC preclinical models. However, few studies are available on primary CSC cultures derived from human postsurgical BC samples, likely because of the limited amount of tissue available after surgery. In this context, comparative oncology is acquiring a relevant role in cancer research, allowing the analysis of larger samples from spontaneous pet tumors that represent optimal models for human cancer.
机译:背景癌症干细胞(CSC)被认为是导致乳腺癌(BC)引发,生长和复发的细胞亚群。 CSC被鉴定为自我更新和肿瘤引发的细胞,赋予多种瘤形成对化学疗法和放射疗法的抵抗力。如今,CSC的药理靶向(约10mM)被认为是不可理解的治疗目标。据报道,抗糖尿病药物二甲双胍可抑制不同肿瘤,特别是在BC临床前模型中的体外和体内CSC存活。然而,关于人类手术后BC样本衍生的原代CSC培养物的研究很少,这可能是因为手术后可用的组织数量有限。在这种情况下,比较肿瘤学正在癌症研究中发挥重要作用,从而可以分析代表人类癌症最佳模型的自发性宠物肿瘤的较大样本。

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