Physiological and pathological roles of Hic‑5 in several organs (Review)

Int J Mol Med. 2022 Nov;50(5):138. doi: 10.3892/ijmm.2022.5194. Epub 2022 Oct 12.

Abstract

Integrins allow cells to adhere to the extracellular matrix and promote the recruitment of other integrins, resulting in the formation of focal adhesion sites at the binding sites. Focal adhesion sites play essential roles in the assembly of the cytoskeleton and are vital in shaping the structure of cells. They also play other regulatory roles by influencing numerous biological functions, such as cell proliferation and apoptosis. Hydrogen peroxide‑inducible clone 5 (Hic‑5) is a member of the Paxillin family of proteins and is an adhesive plaque scaffolding protein. Its expression can be detected in both vascular and smooth muscle cells. Thus, it plays an essential role in vascular remodeling, as well as in fibrotic diseases. Hic‑5 functions as a coactivator of steroid receptors, thus playing a role in steroid hormone‑dependent diseases. It also plays a vital role in the invasive metastasis of various types of cancer. Moreover, several studies have demonstrated that Hic‑5 plays a critical role in transcriptional regulation, as well as in numerous signaling pathways. Therefore, the inhibition of the functions of Hic‑5 may prevent the development or halt the progression of several diseases. Its use as a therapeutic target in future investigations may thus aid in the treatment of several diseases, including various types of cancer. The present review article focused on the expression and functions of Hic‑5 in different organs, with the aim of highlighting novel possibilities for future research.

Keywords: focal adhesion sites; hydrogen peroxide‑inducible clone 5; pathological function; physiological function.

Publication types

  • Review

MeSH terms

  • Cell Adhesion / physiology
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism
  • Hormones
  • Hydrogen Peroxide* / metabolism
  • Integrins* / metabolism
  • Paxillin / metabolism
  • Phosphorylation

Substances

  • Hormones
  • Integrins
  • Paxillin
  • Hydrogen Peroxide
  • Focal Adhesion Protein-Tyrosine Kinases

Grants and funding

The present study was supported by grants from the National Natural Science Foundation of China (grant nos. 81960507, 82073087 and 82160112), and the Collaborative Innovation Center of Chinese Ministry of Education (2020-39), the Science and Technology Bureau fund of Zunyi City [grant no. ZUN SHI KE HE HZ ZI (2019)93-Hao] and the Science and Technology Plan Project of Guizhou Province [grant nos. QIAN KE HE JI CHU-ZK (2021) YI BAN451 and QIAN KE HE LH ZI (2017)7095 HAO].