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EMBO J. 2017 Nov 15;36(22):3325-3335. doi: 10.15252/embj.201797609. Epub 2017 Sep 28.

LncRNA wires up Hippo and Hedgehog signaling to reprogramme glucose metabolism.

Author information

1
College of Life Sciences, Zhejiang University, Hangzhou, Zhejiang, China.
2
Department of Developmental and Cell Biology, University of California, Irvine, Irvine, CA, USA.
3
Division of Surgical Science, Department of Surgery, School of Medicine, Duke University, Durham, NC, USA.
4
Department of Developmental and Cell Biology, University of California, Irvine, Irvine, CA, USA wenqiw6@uci.edu linaifu@zju.edu.cn.
5
College of Life Sciences, Zhejiang University, Hangzhou, Zhejiang, China wenqiw6@uci.edu linaifu@zju.edu.cn.

Abstract

The Hippo pathway plays essential roles in organ size control and cancer prevention via restricting its downstream effector, Yes-associated protein (YAP). Previous studies have revealed an oncogenic function of YAP in reprogramming glucose metabolism, while the underlying mechanism remains to be fully clarified. Accumulating evidence suggests long noncoding RNAs (lncRNAs) as attractive therapeutic targets, given their roles in modulating various cancer-related signaling pathways. In this study, we report that lncRNA breast cancer anti-estrogen resistance 4 (BCAR4) is required for YAP-dependent glycolysis. Mechanistically, YAP promotes the expression of BCAR4, which subsequently coordinates the Hedgehog signaling to enhance the transcription of glycolysis activators HK2 and PFKFB3. Therapeutic delivery of locked nucleic acids (LNAs) targeting BCAR4 attenuated YAP-dependent glycolysis and tumor growth. The expression levels of BCAR4 and YAP are positively correlated in tissue samples from breast cancer patients, where high expression of both BCAR4 and YAP is associated with poor patient survival outcome. Taken together, our study not only reveals the mechanism by which YAP reprograms glucose metabolism, but also highlights the therapeutic potential of targeting YAP-BCAR4-glycolysis axis for breast cancer treatment.

KEYWORDS:

HK2; Hippo pathway; LncRNA; Yes‐associated protein; glycolysis

PMID:
28963395
PMCID:
PMC5686550
[Available on 2018-11-15]
DOI:
10.15252/embj.201797609
[Indexed for MEDLINE]

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