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Identifying an ovarian cancer cell hierarchy regulated by bone morphogenetic protein 2
Author(s) -
YunJung Choi,
Patrick Ingram,
Kun Yang,
Lan Coffman,
M. R. S. Iyengar,
Shoumei Bai,
Dafydd G. Thomas,
Euisik Yoon,
Ronald J. Buckanovich
Publication year - 2015
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1507899112
Subject(s) - bone morphogenetic protein 2 , aldehyde dehydrogenase , cancer stem cell , cancer research , biology , ovarian cancer , cell growth , progenitor cell , cancer cell , microbiology and biotechnology , cellular differentiation , stem cell , cancer , in vitro , genetics , gene
Significance Significant controversy persists regarding a hierarchical vs. stochastic model of cancer. Using a microfluidic single-cell culture device, we define for the first time, to our knowledge, the differentiation capacity of primary human ovarian cancer cells. We demonstrate that ovarian cancer follows a hierarchical model with rare stochastic events. Defining the differentiation capacity allowed us to explain apparently paradoxical actions of bone morphologenetic protein 2 (BMP2); BMP2 suppresses growth in vitro by suppressing bulk cell proliferation, but promotes growth in vivo by promoting cancer stem-like cell (CSC) expansion. This work supports BMP2 signaling as a critical therapeutic target regulating ovarian CSC growth.

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