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

Published

Journal Article

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.

Full Text

Duke Authors

Cited Authors

  • Zheng, X; Han, H; Liu, G-P; Ma, Y-X; Pan, R-L; Sang, L-J; Li, R-H; Yang, L-J; Marks, JR; Wang, W; Lin, A

Published Date

  • November 2017

Published In

Volume / Issue

  • 36 / 22

Start / End Page

  • 3325 - 3335

PubMed ID

  • 28963395

Pubmed Central ID

  • 28963395

Electronic International Standard Serial Number (EISSN)

  • 1460-2075

International Standard Serial Number (ISSN)

  • 0261-4189

Digital Object Identifier (DOI)

  • 10.15252/embj.201797609

Language

  • eng