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间充质干细胞对肺癌细胞系异质细胞群体的影响差异。

Differential effects of mesenchymal stem cells on a heterogeneous cell population within lung cancer cell lines.

机构信息

Department of Respiratory, Southwest Hospital, Third Military Medical University of PLA, Shapingba District, Chongqing, China.

出版信息

Mol Cell Biochem. 2013 Jun;378(1-2):107-16. doi: 10.1007/s11010-013-1600-3. Epub 2013 Mar 3.

Abstract

Although mesenchymal stem cells (MSCs) promote lung cancer growth in vivo, in vitro studies indicate that they inhibit the proliferation of lung cancer cells. Because malignant tumors contain a heterogeneous cell population with variable capacity for self-renewal, the aim of this study was to determine whether the inconsistencies between in vitro and in vivo studies are a result of differential effects of MSCs on the heterogeneous cell population within lung cancer cell lines. Human MSCs were isolated from the bone marrow, and their cell surface antigen expression and multi-lineage differentiation capacity was examined at passage 10. CD133+ cells were isolated from A549 and H446 cell lines using immunomagnetic separation. The effects of MSCs on the growth and microsphere formation of heterogeneous cell populations within two lung cancer cell lines (A549 and H446) were compared. MSCs inhibited the in vitro proliferation of both cell lines, but significantly accelerated tumor formation and stimulated tumor growth in vivo (P < 0.05). In CD133+ cells isolated from both A549 and H446 cells, co-culture with MSCs for 1-3 days significantly increased their proliferation (P < 0.05). MSCs also significantly increased microsphere formation in both cell lines (P < 0.05). Selective stimulation of CD133+ cell growth may account for the discrepant effects of MSCs on lung cancer progression.

摘要

虽然间充质干细胞(MSCs)在体内促进肺癌生长,但体外研究表明它们抑制肺癌细胞的增殖。由于恶性肿瘤包含具有不同自我更新能力的异质性细胞群体,本研究旨在确定体外和体内研究之间的不一致是否是由于 MSCs 对肺癌细胞系内异质性细胞群体的不同影响所致。从骨髓中分离出人间充质干细胞,并在第 10 代时检查其细胞表面抗原表达和多谱系分化能力。使用免疫磁珠分离法从 A549 和 H446 细胞系中分离出 CD133+细胞。比较了 MSCs 对两种肺癌细胞系(A549 和 H446)内异质性细胞群体的生长和微球体形成的影响。MSCs 抑制了两种细胞系的体外增殖,但显着加速了肿瘤的形成并刺激了体内肿瘤的生长(P <0.05)。在从 A549 和 H446 细胞中分离出的 CD133+细胞中,与 MSCs 共培养 1-3 天显着增加了它们的增殖(P <0.05)。MSCs 还显着增加了两种细胞系中的微球体形成(P <0.05)。CD133+细胞生长的选择性刺激可能解释了 MSCs 对肺癌进展的不同影响。

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