TY - JOUR
T1 - NF-κB non-cell-autonomously regulates cancer stem cell populations in the basal-like breast cancer subtype
AU - Yamamoto, Mizuki
AU - Taguchi, Yuu
AU - Ito-Kureha, Taku
AU - Semba, Kentaro
AU - Yamaguchi, Noritaka
AU - Inoue, Jun Ichiro
N1 - Funding Information:
We thank T. Akiyama, J. Gohda and A. Niida for their helpful input and K. Miyazaki for secretarial assistance. This work was partially supported by a grant-in-aid for Scientific Research on Innovative Areas and by a contract research fund for the Program of Japan Initiative for Global Research Network on Infectious Diseases from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (J-i.I.), by the Takeda Science Foundation (J.-i.I.). M.Y. is a research fellow of the Japan Society for the Promotion of Science.
PY - 2013
Y1 - 2013
N2 - Patients with triple-negative breast cancer display the highest rates of early relapse of all patients with breast cancer. The basal-like subtype, a subgroup of triple-negative breast cancer, exhibits high levels of constitutively active NF-κB signalling. Here we show that NF-κB activation, induced by inflammatory cytokines or by epigenetically dysregulated NIK expression, cell-autonomously upregulates JAG1 expression in non-cancer stem cells. This upregulation stimulates NOTCH signalling in cancer stem cells in trans, leading to an expansion of cancer stem cell populations. Among breast cancers, the NF-κB-dependent induction of JAG1 and the NOTCH-dependent expansion of the cancer stem cell population occur only in the basal-like subtype. Collectively, our results indicate that NF-κB has a non-cell-autonomous role in regulating cancer stem cell populations by forming intratumoural microenvironments composed of JAG1-expressing non-cancer stem cells with a basal-like subtype.
AB - Patients with triple-negative breast cancer display the highest rates of early relapse of all patients with breast cancer. The basal-like subtype, a subgroup of triple-negative breast cancer, exhibits high levels of constitutively active NF-κB signalling. Here we show that NF-κB activation, induced by inflammatory cytokines or by epigenetically dysregulated NIK expression, cell-autonomously upregulates JAG1 expression in non-cancer stem cells. This upregulation stimulates NOTCH signalling in cancer stem cells in trans, leading to an expansion of cancer stem cell populations. Among breast cancers, the NF-κB-dependent induction of JAG1 and the NOTCH-dependent expansion of the cancer stem cell population occur only in the basal-like subtype. Collectively, our results indicate that NF-κB has a non-cell-autonomous role in regulating cancer stem cell populations by forming intratumoural microenvironments composed of JAG1-expressing non-cancer stem cells with a basal-like subtype.
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U2 - 10.1038/ncomms3299
DO - 10.1038/ncomms3299
M3 - Article
C2 - 23934482
AN - SCOPUS:84883097117
SN - 2041-1723
VL - 4
JO - Nature communications
JF - Nature communications
M1 - 2299
ER -