TY - JOUR
T1 - Loss-of-function screens of druggable targetome against cancer stem-like cells
AU - Song, Mee
AU - Lee, Hani
AU - Nam, Myung Hee
AU - Jeong, Euna
AU - Kim, Somin
AU - Hong, Yourae
AU - Kim, Nayoung
AU - Yim, Hwa Young
AU - Yoo, Young Ji
AU - Kim, Jung Seok
AU - Kim, Jin Seok
AU - Cho, Yong Yeon
AU - Mills, Gordon B.
AU - Kim, Woo Young
AU - Yoon, Sukjoon
N1 - Publisher Copyright:
© The Author(s).
PY - 2017/2
Y1 - 2017/2
N2 - Cancer stem-like cells (CSLCs) contribute to the initiation andrecurrence of tumorsandto their resistance to conventional therapies. In this study, small interfering RNA (siRNA)-based screening of ∼4800 druggable genes in 3-dimensionalCSLCcultures in comparison to 2-dimensional bulk cultures of U87 glioma cells revealed 3 groups of genes essential for the following: survival of the CSLC population only, bulk-cultured population only, or both populations.While diverse biologic processes were associatedwith siRNAs reducing the bulk-cultured population, CSLC-eliminating siRNAs were enriched in a few functional categories, such as lipid metabolism, protein metabolism, and gene expression. Interestingly, siRNAs that selectively reduced CSLC only were found to target genes for cholesterol and unsaturated fatty acid synthesis. The lipidomic profile of CSLCs revealed increased levels of monounsaturated lipids. Pharmacologic blockage of these target pathways reduced CSLCs, and this effect was eliminated by addition of downstream metabolite products. The present CSLC-sensitive target categories provide a useful resource that can be exploited for the selective elimination ofCSLCs.-Song, M., Lee, H., Nam, M.-H., Jeong, E., Kim, S., Hong, Y., Kim, N., Yim, H. Y., Yoo, Y.-J., Kim, J. S., Kim, J.-S., Cho, Y.-Y., Mills, G. B., Kim, W.-Y., Yoon, S. Loss-offunction screens of druggable targetome against cancer stem-like cells. FASEB J. 31, 625-635 (2017).www.fasebj.org.
AB - Cancer stem-like cells (CSLCs) contribute to the initiation andrecurrence of tumorsandto their resistance to conventional therapies. In this study, small interfering RNA (siRNA)-based screening of ∼4800 druggable genes in 3-dimensionalCSLCcultures in comparison to 2-dimensional bulk cultures of U87 glioma cells revealed 3 groups of genes essential for the following: survival of the CSLC population only, bulk-cultured population only, or both populations.While diverse biologic processes were associatedwith siRNAs reducing the bulk-cultured population, CSLC-eliminating siRNAs were enriched in a few functional categories, such as lipid metabolism, protein metabolism, and gene expression. Interestingly, siRNAs that selectively reduced CSLC only were found to target genes for cholesterol and unsaturated fatty acid synthesis. The lipidomic profile of CSLCs revealed increased levels of monounsaturated lipids. Pharmacologic blockage of these target pathways reduced CSLCs, and this effect was eliminated by addition of downstream metabolite products. The present CSLC-sensitive target categories provide a useful resource that can be exploited for the selective elimination ofCSLCs.-Song, M., Lee, H., Nam, M.-H., Jeong, E., Kim, S., Hong, Y., Kim, N., Yim, H. Y., Yoo, Y.-J., Kim, J. S., Kim, J.-S., Cho, Y.-Y., Mills, G. B., Kim, W.-Y., Yoon, S. Loss-offunction screens of druggable targetome against cancer stem-like cells. FASEB J. 31, 625-635 (2017).www.fasebj.org.
KW - CSLC sphere culture
KW - Lipid profile
KW - Network analysis
KW - siRNA screening
UR - http://www.scopus.com/inward/record.url?scp=85011286354&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85011286354&partnerID=8YFLogxK
U2 - 10.1096/fj.201600953
DO - 10.1096/fj.201600953
M3 - Article
C2 - 27811063
AN - SCOPUS:85011286354
SN - 0892-6638
VL - 31
SP - 625
EP - 935
JO - FASEB Journal
JF - FASEB Journal
IS - 2
ER -