Permanently Blocked Stem Cells Derived From Breast Cancer Cell Lines

Author:

Sajithlal Gangadharan B.1,Rothermund Kristi1,Zhang Fang2,Dabbs David J.3,Latimer Jean J.45,Grant Stephen G.46,Prochownik Edward V.147

Affiliation:

1. Section of Hematology/Oncology, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA

2. The Department of Pharmacology and Chemical Biology, Pittsburgh, Pennsylvania, USA

3. The Department of Pathology, McGee-Women's Hospital, Pittsburgh, Pennsylvania, USA

4. The University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania, USA

5. The Department of Obstetrics, Gynecology and Reproductive Sciences, Pittsburgh, Pennsylvania, USA

6. The Department of Environmental and Occupational Health, and Pittsburgh, Pennsylvania, USA

7. The Department of Microbiology and Molecular Genetics, The University of Pittsburgh Medical Center (UPMC), Pittsburgh, Pennsylvania, USA

Abstract

Abstract Cancer stem cells (CSCs) are thought to be resistant to standard chemotherapeutic drugs and the inimical conditions of the tumor microenvironment. Obtaining CSCs in sufficient quantities and maintaining their undifferentiated state have been major hurdles to their further characterization and to the identification of new pharmaceuticals that preferentially target these cells. We describe here the tagging of CSC-like populations from four human breast cancer cell lines with green fluorescent protein (GFP) under the control of the Oct3/4 stem cell-specific promoter. As expected, GFP was expressed by the CSC-enriched populations. However, an unanticipated result was that these cells remained blocked in a CSC-like state and tended to be resistant to chemotherapeutic drugs as well as acidotic and hypoxic conditions. These CSC-like cells possessed several other in vitro attributes of CSCs and were able to reproducibly generate tumors in immunocompromised mice from as few as 100 cells. Moreover, the tumors derived from these cells were comprised almost exclusively of pure CSCs. The ability of the Oct3/4 promoter to block CSC differentiation underscores its potential general utility for obtaining highly purified CSC populations, although the mechanism by which it does so remains undefined and subject to further study. Nonetheless, such stable cell lines should be extremely valuable tools for studying basic questions pertaining to CSC biology and for the initial identification of novel CSC-specific chemotherapeutic agents, which can then be verified in primary CSCs.

Funder

NIH

Children's Hospital of Pittsburgh of UPMC

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

Reference59 articles.

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