GTSE1 promotes prostate cancer cell proliferation via the SP1/FOXM1 signaling pathway

Lab Invest. 2021 May;101(5):554-563. doi: 10.1038/s41374-020-00510-4. Epub 2020 Dec 16.

Abstract

G2 and S phase-expressed-1 (GTSE1) has been implicated in the pathogenesis of several malignant tumors. However, its specific role in prostate cancer (PCa) remains unclear. In this study, RNA-Seq data from patients with PCa and controls were downloaded from the FIREBROWSE database, and it was found that the GTSE1 mRNA level was significantly upregulated in PCa. Moreover, patients with higher GTSE1 mRNA levels had higher Gleason scores (P < 0.001), a more advanced pT stage (P = 0.011), and a more advanced pN stage (P = 0.006) as well as a shorter time to biochemical recurrence (P = 0.005). In addition, overexpression of GTSE1 could promote proliferation in LNCaP cells, whereas silencing GTSE1 could inhibit the growth of C4-2 cells in vitro and in vivo. Mechanistically, GTSE1 enhanced the expression of FOXM1 by upregulating the SP1 protein level, a transcription factor of FOXM1, which ultimately promoted PCa cell proliferation. In summary, GTSE1 is a new candidate oncogene in the development and progression of PCa, and it can promote PCa cell proliferation via the SP1/FOXM1 signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Proliferation
  • Forkhead Box Protein M1 / metabolism*
  • Humans
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Microtubule-Associated Proteins / genetics*
  • Prostatic Neoplasms / etiology*
  • Prostatic Neoplasms / metabolism
  • Signal Transduction
  • Sp1 Transcription Factor / metabolism*

Substances

  • FOXM1 protein, human
  • Forkhead Box Protein M1
  • GTSE1 protein, human
  • Microtubule-Associated Proteins
  • Sp1 Transcription Factor
  • SP1 protein, human