Please use this identifier to cite or link to this item: https://doi.org/10.1111/jnc.12199
Title: Inhibition of neuronal nitric oxide synthase activity promotes migration of human-induced pluripotent stem cell-derived neural stem cells toward cancer cells
Authors: Chen, C.
Wang, Y.
Goh, S.S.L.
Yang, J.
Lam, D.H.
Choudhury, Y.
Tay, F.C.
Du, S.
Tan, W.K.
Purwanti, Y.I.
Fan, W.
Wang, S. 
Keywords: Boyden chamber assay
microarray analysis
Neural stem cells
neuronal nitric oxide synthase
tumor tropism
Issue Date: Aug-2013
Citation: Chen, C., Wang, Y., Goh, S.S.L., Yang, J., Lam, D.H., Choudhury, Y., Tay, F.C., Du, S., Tan, W.K., Purwanti, Y.I., Fan, W., Wang, S. (2013-08). Inhibition of neuronal nitric oxide synthase activity promotes migration of human-induced pluripotent stem cell-derived neural stem cells toward cancer cells. Journal of Neurochemistry 126 (3) : 318-330. ScholarBank@NUS Repository. https://doi.org/10.1111/jnc.12199
Abstract: The breakthrough in derivation of human-induced pluripotent stem cells (hiPSCs) provides an approach that may help overcome ethical and allergenic challenges posed in numerous medical applications involving human cells, including neural stem/progenitor cells (NSCs). Considering the great potential of NSCs in targeted cancer gene therapy, we investigated in this study the tumor tropism of hiPSC-derived NSCs and attempted to enhance the tropism by manipulation of biological activities of proteins that are involved in regulating the migration of NSCs toward cancer cells. We first demonstrated that hiPSC-NSCs displayed tropism for both glioblastoma cells and breast cancer cells in vitro and in vivo. We then compared gene expression profiles between migratory and non-migratory hiPSC-NSCs toward these cancer cells and observed that the gene encoding neuronal nitric oxide synthase (nNOS) was down-regulated in migratory hiPSC-NSCs. Using nNOS inhibitors and nNOS siRNAs, we demonstrated that this protein is a relevant regulator in controlling migration of hiPSC-NSCs toward cancer cells, and that inhibition of its activity or down-regulation of its expression can sensitize poorly migratory NSCs and be used to improve their tumor tropism. These findings suggest a novel application of nNOS inhibitors in neural stem cell-mediated cancer therapy. © 2013 International Society for Neurochemistry.
Source Title: Journal of Neurochemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/100931
ISSN: 00223042
DOI: 10.1111/jnc.12199
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