TY - JOUR
T1 - The effects of restricted glycolysis on stem-cell like characteristics of breast cancer cells
AU - Banerjee, Arindam
AU - Arvinrad, Pardis
AU - Darley, Matthew
AU - Laversin, Stéphanie A.
AU - Parker, Rachel
AU - Rose-Zerilli, Matthew J.J.
AU - Townsend, Paul A.
AU - Cutress, Ramsey I.
AU - Beers, Stephen A.
AU - Houghton, Franchesca D.
AU - Birts, Charles N.
AU - Blaydes, Jeremy P.
PY - 2018/5/1
Y1 - 2018/5/1
N2 - Altered glycolysis is a characteristic of many cancers, and can also be associated with changes in stem cell-like cancer (SCLC) cell populations. We therefore set out to directly examine the effect of glycolysis on SCLC cell phenotype, using a model where glycolysis is stably reduced by adapting the cells to a sugar source other than glucose. Restricting glycolysis using this approach consistently resulted in cells with increased oncogenic potential; including an increase in SCLC cells, proliferation in 3D matrigel, invasiveness, chemoresistance, and altered global gene expression. Tumorigenicity in vivo was also markedly increased. SCLC cells exhibited increased dependence upon alternate metabolic pathways. They also became c-KIT dependent, indicating that their apparent state of maturation is regulated by glycolysis. Single-cell mRNA sequencing identified altered networks of metabolic-, stem- and signaling- gene expression within SCLC-enriched populations in response to glycolytic restriction. Therefore, reduced glycolysis, which may occur in niches within tumors where glucose availability is limiting, can promote tumor aggressiveness by increasing SCLC cell populations, but can also introduce novel, potentially exploitable, vulnerabilities in SCLC cells.
AB - Altered glycolysis is a characteristic of many cancers, and can also be associated with changes in stem cell-like cancer (SCLC) cell populations. We therefore set out to directly examine the effect of glycolysis on SCLC cell phenotype, using a model where glycolysis is stably reduced by adapting the cells to a sugar source other than glucose. Restricting glycolysis using this approach consistently resulted in cells with increased oncogenic potential; including an increase in SCLC cells, proliferation in 3D matrigel, invasiveness, chemoresistance, and altered global gene expression. Tumorigenicity in vivo was also markedly increased. SCLC cells exhibited increased dependence upon alternate metabolic pathways. They also became c-KIT dependent, indicating that their apparent state of maturation is regulated by glycolysis. Single-cell mRNA sequencing identified altered networks of metabolic-, stem- and signaling- gene expression within SCLC-enriched populations in response to glycolytic restriction. Therefore, reduced glycolysis, which may occur in niches within tumors where glucose availability is limiting, can promote tumor aggressiveness by increasing SCLC cell populations, but can also introduce novel, potentially exploitable, vulnerabilities in SCLC cells.
KW - Breast cancer stem cell-like cells
KW - Chemoresistance
KW - Glycolysis
KW - Metabolism
KW - Single-cell mRNA-seq
UR - http://www.scopus.com/inward/record.url?scp=85046775317&partnerID=8YFLogxK
U2 - 10.18632/oncotarget.25299
DO - 10.18632/oncotarget.25299
M3 - Article
AN - SCOPUS:85046775317
SN - 1949-2553
VL - 9
SP - 23274
EP - 23288
JO - Oncotarget
JF - Oncotarget
IS - 33
ER -