Regulation of Hippo signaling by metabolic pathways in cancer

Biochim Biophys Acta Mol Cell Res. 2022 Apr;1869(4):119201. doi: 10.1016/j.bbamcr.2021.119201. Epub 2022 Jan 11.

Abstract

Hippo signaling is known to maintain balance between cell proliferation and apoptosis via tight regulation of factors, such as metabolic cues, cell-cell contact, and mechanical cues. Cells directly recognize glucose, lipids, and other metabolic cues and integrate multiple signaling pathways, including Hippo signaling, to adjust their proliferation and apoptosis depending on nutrient conditions. Therefore, the dysregulation of the Hippo signaling pathway can promote tumor initiation and progression. Alteration in metabolic cues is considered a major factor affecting the risk of cancer formation and progression. It has recently been shown that the dysregulation of the Hippo signaling pathway, through diverse routes activated by metabolic cues, can lead to cancer with a poor prognosis. In addition, unique crosstalk between metabolic pathways and Hippo signaling pathways can inhibit the effect of anticancer drugs and promote drug resistance. In this review, we describe an integrated perspective of the relationship between the Hippo signaling pathway and metabolic signals in the context of cancer. We also characterize the mechanisms involved in changes in metabolism that are linked to the Hippo signaling pathway in the cancer microenvironment and propose several novel targets for anticancer drug treatment.

Keywords: Drug resistance; Glucose; Hippo signaling pathway; Lipids; Metabolism.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Glucose / metabolism
  • Hippo Signaling Pathway* / drug effects
  • Hippo Signaling Pathway* / genetics
  • Humans
  • Lipid Metabolism / genetics
  • Metabolic Networks and Pathways* / genetics
  • Neoplasms / drug therapy
  • Neoplasms / metabolism
  • Neoplasms / pathology*
  • Receptors, G-Protein-Coupled / metabolism
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Antineoplastic Agents
  • Receptors, G-Protein-Coupled
  • TOR Serine-Threonine Kinases
  • Glucose