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生物工程化类癌干细胞的设计与表征

Design and Characterization of Bioengineered Cancer-Like Stem Cells.

作者信息

Cho Sungpil, Park Hongsuk, Jarboe Elke A, Peterson C Matthew, Bae You Han, Janát-Amsbury Margit M

机构信息

Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Salt Lake City, Utah, United States of America.

Department of Bioengineering, Salt Lake City, Utah, United States of America.

出版信息

PLoS One. 2015 Oct 21;10(10):e0141172. doi: 10.1371/journal.pone.0141172. eCollection 2015.

Abstract

Cancer stem cells (CSCs) are a small subset of cancer cells responsible for maintenance and progression of several types of cancer. Isolation, propagation, and the differentiation of CSCs in the proper stem niches expose the intrinsic difficulties for further studies. Here we show that induced cancer like stem cells (iCLSCs) can be generated by in vitro oncogenic manipulation of mouse embryonic stem cells (mESCs) with well-defined oncogenic elements; SV40 LTg and HrasV12 by using a mouse stem virus long terminal repeat (MSCV-LTR)-based retroviral system. The reprogrammed mESCs using both oncogenes were characterized through their oncogenic gene expression, the enhancement of proliferation, and unhampered maintenance of stem properties in vitro and in vivo. In addition, these transformed cells resulted in the formation of malignant, immature ovarian teratomas in vivo. To successfully further expand these properties to other organs and species, more research needs to be done to fully understand the role of a tumor- favorable microenvironment. Our current study has provided a novel approach to generate induced cancer like stem cells through in vitro oncogenic reprogramming and successfully initiated organ-specific malignant tumor formation in an orthotopic small animal cancer model.

摘要

癌症干细胞(CSCs)是一小部分癌细胞,负责多种癌症的维持和进展。在合适的干细胞生态位中分离、增殖和分化CSCs给进一步研究带来了内在困难。在此,我们表明,通过使用基于小鼠干细胞病毒长末端重复序列(MSCV-LTR)的逆转录病毒系统,用明确的致癌元件(SV40 LTg和HrasV12)对小鼠胚胎干细胞(mESCs)进行体外致癌操作,可以产生诱导性类癌干细胞(iCLSCs)。使用这两种癌基因对重编程的mESCs进行了表征,通过其致癌基因表达、增殖增强以及在体外和体内对干细胞特性的不受阻碍的维持。此外,这些转化细胞在体内导致了恶性、不成熟的卵巢畸胎瘤的形成。为了成功地将这些特性进一步扩展到其他器官和物种,需要进行更多研究以充分了解有利于肿瘤的微环境的作用。我们目前的研究提供了一种通过体外致癌重编程产生诱导性类癌干细胞的新方法,并在原位小动物癌症模型中成功启动了器官特异性恶性肿瘤的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/154d/4619203/cef3a59e740e/pone.0141172.g001.jpg

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