Understanding the mechanisms involved in the induction and maintenance of cancer stem cells (CSCs) is critical for developing therapies that can target CSCs effectively. Increasing evidence has suggested such mechanisms are often shared by both CSCs and normal stem cells. Therefore, studies in normal stem cells yield important insights into the cancer stem cell biology. The epithelial-mesenchymal transition has been shown to confer differentiated mammary epithelial cells stem cell-like properties (Mani et al. Cell 2008). However, it is not clear whether the EMT plays a role in bona fide mammary stem cell induction and maintenance. It is also not yet rigorously demonstrated that the EMT can induce breast cancer stem cells. In addition, the mechanism by which the EMT activates stem-cell program is unknown. To examine the role of the EMT in the induction of stem cells, primary mammary epithelial cells (MECs) and cancer cells will be induced to undergo transient EMTs, and then tested for increases in stem cell activities. The ability of EMTs in converting differentiated cells into stem cells will also be tested. Loss-of-function approaches, including gene knock-out and knock-down, will be used to test the requirement of EMT- inducing factors in the maintenance of mammary stem cells and breast cancer stem cells. The involvement of stem cell-related signaling pathways in mediating the activation of the stem-cell program by the EMT will be also examined in this proposal. Positive outcomes ofthese studies will lead to better understanding ofthe biology of normal stem cells and cancer stem cells and help developing cancer stem cell-targeted therapies. In addition, understanding the link of EMT and bona fide stem cells will help generating normal epithelial stem cells for research and therapeutic uses.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32CA144404-02
Application #
8193999
Study Section
Special Emphasis Panel (ZRG1-F09-A (20))
Program Officer
Jakowlew, Sonia B
Project Start
2010-09-15
Project End
2013-09-14
Budget Start
2011-09-15
Budget End
2012-09-14
Support Year
2
Fiscal Year
2011
Total Cost
$58,682
Indirect Cost
Name
Whitehead Institute for Biomedical Research
Department
Type
DUNS #
120989983
City
Cambridge
State
MA
Country
United States
Zip Code
02142
Guo, Wenjun; Keckesova, Zuzana; Donaher, Joana Liu et al. (2012) Slug and Sox9 cooperatively determine the mammary stem cell state. Cell 148:1015-28
Scheel, Christina; Eaton, Elinor Ng; Li, Sophia Hsin-Jung et al. (2011) Paracrine and autocrine signals induce and maintain mesenchymal and stem cell states in the breast. Cell 145:926-40