Knockdown of GSG2 inhibits the development and progression of non-small cell lung cancer in vitro and in vivo

Cell Cycle. 2023 Jan;22(2):153-164. doi: 10.1080/15384101.2022.2110441. Epub 2022 Aug 16.

Abstract

Lung cancer has been recognized as the most common malignant neoplasm of the respiratory system with extremely high morbidity, among which non-small cell lung cancer (NSCLC) accounts for the majority. Many published literatures have revealed the roles of GSG2 in the progression of ovarian cancer, bladder cancer and breast cancer. However, there were no reports on the relationship between GSG2 and NSCLC. Herein, GSG2 was identified as a potential tumor promoter in NSCLC development, whose abundant expression was observed in NSCLC tissues compared with adjacent nonmalignant tissues and statistically correlated with more advanced tumor stage, more malignant grade and higher risk of lymphatic metastasis. Subsequent in vitro loss-of-function experiments indicated that GSG2 depletion could arrest cell cycle and suppress cell proliferation and migration while enhancing cell apoptosis. At the same time, the suppressive effects of GSG2 depletion on NSCLC development were verified by in vivo experiments. In conclusion, the current study identified GSG2 as a tumor promoter in development and progression of NSCLC, which could work as a novel therapeutic target for NSCLC.

Keywords: GSG2; NSCLC; cell apoptosis; cell migration; cell proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinogens
  • Carcinoma, Non-Small-Cell Lung* / pathology
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Proliferation / genetics
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Lung Neoplasms* / pathology
  • MicroRNAs* / metabolism

Substances

  • Carcinogens
  • MicroRNAs

Grants and funding

The work was supported by the Cams Initiative For Innovative Medicine (cams-i2m) [2017-i2m-003] []; Beijing hope run special fund of cancer foundation of china lc2017b20 [].