Increased expression of SRPK1 (serine/arginine-rich protein-specific kinase 1) is associated with progression and unfavorable prognosis in cervical squamous cell carcinoma

Bioengineered. 2022 Mar;13(3):6100-6112. doi: 10.1080/21655979.2022.2034705.

Abstract

Previous studies suggest that SRPK1 (serine/arginine-rich protein-specific kinase 1) is involved in tumorigenesis and closely related to unfavorable outcomes. However, its expression pattern in cervical squamous cell carcinoma (CESC) remains uncovered. In this study, we initially investigated the clinical significance and function of SRPK1 in human CESC. Data mining and analysis on SRPK1 mRNA expression in CESC samples were conducted using TCGA database, which indicated that SRPK1 mRNA was significantly upregulated in CESC samples. Protein expression of SRPK1 was tested by immunohistochemistry in a retrospective cohort (n = 122), revealing a higher SRPK1 protein abundance in CESC specimens whose aberrant up-regulation was obviously related to worse survival. Cox proportional hazards regression analysis further confirmed the role of SRPK1 as an independent prognostic factor of CESC. Cellular experiments validated that SRPK1 may function through enhancing CESC proliferation, migration, and invasion. In conclusion, aberrant up-regulation of SRPK1 is remarkably related to progression and unfavorable prognosis of CESC, which can serve as a novel prognostic biomarker and therapeutic target for CESC.

Keywords: Cervical squamous cell carcinoma; invasion; prognosis; proliferation; serine/arginine-rich protein-specific kinase 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arginine
  • Carcinoma, Squamous Cell* / diagnosis
  • Carcinoma, Squamous Cell* / genetics
  • Carcinoma, Squamous Cell* / metabolism
  • Female
  • Humans
  • Prognosis
  • Protein Serine-Threonine Kinases / genetics
  • RNA, Messenger / genetics
  • Retrospective Studies
  • Serine
  • Uterine Cervical Neoplasms* / metabolism

Substances

  • Arginine
  • Protein Serine-Threonine Kinases
  • RNA, Messenger
  • Serine
  • SRPK1 protein, human

Grants and funding

This study was supported by the National Natural Science Foundation of China (No. 81860528).