Author
Listed:
- Tackhoon Kim
(Korea Advanced Institute of Science and Technology
Korea Advanced Institute of Science and Technology)
- Suk-Jin Yang
(Medical Genomics Research Center, Korea Research Institute of Bioscience and Biotechnology)
- Daehee Hwang
(Korea Advanced Institute of Science and Technology
Korea Advanced Institute of Science and Technology)
- Jinhoi Song
(Therapeutic Antibody Research Center, Korea Research Institute of Bioscience and Biotechnology)
- Minchul Kim
(Korea Advanced Institute of Science and Technology
Korea Advanced Institute of Science and Technology)
- Sang Kyum Kim
(Yonsei University College of Medicine)
- Keunsoo Kang
(Korea Advanced Institute of Science and Technology)
- Jaebum Ahn
(Korea Advanced Institute of Science and Technology
Korea Advanced Institute of Science and Technology)
- Daeyoup Lee
(Korea Advanced Institute of Science and Technology)
- Mi-young Kim
(Korea Advanced Institute of Science and Technology)
- Seyun Kim
(Korea Advanced Institute of Science and Technology)
- Ja Seung Koo
(Yonsei University College of Medicine)
- Sang Seok Koh
(Dong-A University)
- Seon-Young Kim
(Medical Genomics Research Center, Korea Research Institute of Bioscience and Biotechnology)
- Dae-Sik Lim
(Korea Advanced Institute of Science and Technology)
Abstract
The switch between stem/progenitor cell expansion and differentiation is critical for organ homeostasis. The mammalian Hippo pathway effector and oncoprotein YAP expands undifferentiated stem/progenitor cells in various tissues. However, the YAP-associated transcription factors and downstream targets underlying this stemness-promoting activity are poorly understood. Here we show that the SRF–IL6 axis is the critical mediator of YAP-induced stemness in mammary epithelial cells and breast cancer. Specifically, serum response factor (SRF)-mediated binding and recruitment of YAP to mammary stem cell (MaSC) signature-gene promoters induce numerous MaSC signature genes, among which the target interleukin (IL)-6 is critical for YAP-induced stemness. High SRF–YAP/TAZ expression is correlated with IL6-enriched MaSC/basal-like breast cancer (BLBC). Finally, we show that this high SRF expression enables YAP to more efficiently induce IL6 and stemness in BLBC compared with luminal-type breast cancer. Collectively, our results establish the importance of SRF–YAP–IL6 signalling in promoting MaSC-like properties in a BLBC-specific manner.
Suggested Citation
Tackhoon Kim & Suk-Jin Yang & Daehee Hwang & Jinhoi Song & Minchul Kim & Sang Kyum Kim & Keunsoo Kang & Jaebum Ahn & Daeyoup Lee & Mi-young Kim & Seyun Kim & Ja Seung Koo & Sang Seok Koh & Seon-Young , 2015.
"A basal-like breast cancer-specific role for SRF–IL6 in YAP-induced cancer stemness,"
Nature Communications, Nature, vol. 6(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms10186
DOI: 10.1038/ncomms10186
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