Roles of protein tyrosine phosphatases in hepatocellular carcinoma progression (Review)

Oncol Rep. 2023 Mar;49(3):48. doi: 10.3892/or.2023.8485. Epub 2023 Jan 20.

Abstract

Hepatocellular carcinoma (HCC) represents almost 80% of all liver cancers, is the sixth most common cancer and is the second‑highest cause of cancer‑related deaths worldwide. Protein tyrosine phosphatases (PTPs), which are encoded by the largest family of phosphatase genes, play critical roles in cellular responses and are implicated in various signaling pathways. Moreover, PTPs are dysregulated and involved in various cellular processes in numerous cancers, including HCC. Kinases and phosphatases are coordinators that modulate cell activities and regulate signaling responses. There are multiple interacting signaling networks, and coordination of these signaling networks in response to a stimulus determines the physiological outcome. Numerous issues, such as drug resistance and inflammatory reactions in the tumor microenvironment, are implicated in cancer progression, and the role of PTPs in these processes has not been well elucidated. Therefore, the present review focused on discussing the relationship of PTPs with inflammatory cytokines and chemotherapy/targeted drug resistance, providing detailed information on how PTPs can modulate inflammatory reactions and drug resistance to influence progression in HCC.

Keywords: drug resistance; hepatocellular carcinoma; inflammation; protein tyrosine phosphatases.

Publication types

  • Review

MeSH terms

  • Carcinoma, Hepatocellular* / drug therapy
  • Carcinoma, Hepatocellular* / genetics
  • Humans
  • Inflammation
  • Liver Neoplasms* / drug therapy
  • Liver Neoplasms* / genetics
  • Protein Tyrosine Phosphatases / genetics
  • Protein Tyrosine Phosphatases / metabolism
  • Signal Transduction / genetics
  • Tumor Microenvironment

Substances

  • Protein Tyrosine Phosphatases

Grants and funding

The present study was supported by the Ministry of Science and Technology of the Republic of China (grant nos. MOST 109-2320-B-006-067. and MOST 110-2320-B-039-044).