Differential Radiosensitizing Effect of Valproic Acid in Differentiation Versus Self-Renewal Promoting Culture Conditions

Purpose It has been shown that valproic acid (VA) enhances the proliferation and self-renewal of normal hematopoietic stem cells and that breast cancer stem/progenitor cells can be resistant to radiation. From these data, we hypothesized that VA would fail to radiosensitize breast cancer stem/progen...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2010-03, Vol.76 (3), p.889-895
Hauptverfasser: Debeb, Bisrat G., D.V.M., Ph.D, Xu, Wei, Ph.D, Mok, Henry, M.D., Ph.D, Li, Li, B.S, Robertson, Fredika, Ph.D, Ueno, Naoto T., M.D., Ph.D, Reuben, Jim, Ph.D, Lucci, Anthony, M.D, Cristofanilli, Massimo, M.D, Woodward, Wendy A., M.D., Ph.D
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Sprache:eng
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Zusammenfassung:Purpose It has been shown that valproic acid (VA) enhances the proliferation and self-renewal of normal hematopoietic stem cells and that breast cancer stem/progenitor cells can be resistant to radiation. From these data, we hypothesized that VA would fail to radiosensitize breast cancer stem/progenitor cells grown to three-dimensional (3D) mammospheres. Methods and Materials We used the MCF7 breast cancer cell line grown under stem cell-promoting culture conditions (3D mammosphere) and standard nonstem cell monolayer culture conditions (two-dimensional) to examine the effect of pretreatment with VA on radiation sensitivity in clonogenic survival assays and on the expression of embryonic stem cell transcription factors. Results 3D-cultured MCF-7 cells expressed higher levels of Oct4, Nanog, and Sox2. The 3D passage enriched self-renewal and increased radioresistance in the 3D mammosphere formation assays. VA radiosensitized adherent cells but radioprotected 3D cells in single-fraction clonogenic assays. Moreover, fractionated radiation sensitized VA-treated adherent MCF7 cells but did not have a significant effect on VA-treated single cells grown to mammospheres. Conclusion We have concluded that VA might preferentially radiosensitize differentiated cells compared with those expressing stem cell surrogates and that stem cell-promoting culture is a useful tool for in vitro evaluation of novel cancer therapeutic agents and radiosensitizers.
ISSN:0360-3016
1879-355X
DOI:10.1016/j.ijrobp.2009.09.052