Cohesin subunits, STAG1 and STAG2, and cohesin regulatory factor, PDS5b, in oral squamous cells carcinomas

Josiane Alves França1, Marina Gonçalves Diniz2, Vanessa Fátima Bernardes1

  • 1Department of Pathology, Biological Sciences Institute, Universidade Federal de Minas Gerais-UFMG, Belo Horizonte, Brazil.

Abstract

Insights

Loss of heterozygosity at STAG1 and STAG2 occurs in oral squamous cell carcinoma (OSCC), but gene expression remains similar to normal tissue. PDS5B protein levels were high in OSCC but did not correlate with proliferation markers.

Area of Science:

  • Genetics and Molecular Biology
  • Oncology
  • Cell Biology

Background:

  • The cohesin complex, including STAG1/STAG2, regulates sister chromatid cohesion and is influenced by PDS5B, a cell proliferation inhibitor.
  • Alterations in STAG1, STAG2, and PDS5B have been implicated in various tumors.
  • This study investigates these genes in oral squamous cell carcinoma (OSCC).

Purpose of the Study:

  • To assess molecular alterations of STAG1, STAG2, and PDS5B in OSCC.
  • To predict gene expression based on cell cycle gene profiles.
  • To examine the relationship between PDS5B protein expression and proliferation markers (Ki-67, p53).

Main Methods:

  • Loss of heterozygosity (LOH) analysis for STAG1 and STAG2 using polymorphic markers in 15 OSCC samples.
  • Quantitative PCR (qPCR) to compare STAG1, STAG2, and PDS5B transcript levels between OSCC and normal oral mucosa (NM).
  • Immunohistochemical analysis of PDS5B, Ki-67, and p53 in 62 OSCC samples and multiple linear regression using an 84-gene cell cycle array.

Main Results:

  • LOH was detected at STAG1 and STAG2 loci in a subset of OSCC samples.
  • Transcriptional levels of STAG1, STAG2, and PDS5B were similar between OSCC and NM.
  • High PDS5B, p53, and Ki-67 immunoexpression was observed, but PDS5B levels did not correlate with Ki-67 or p53.
  • A potential relationship was found between STAG1 and CUL3 expression.

Conclusions:

  • While LOH occurs at STAG1 and STAG2 in OSCC, their transcriptional levels are comparable to normal tissue.
  • High PDS5B protein expression in OSCC does not appear to be associated with the proliferation index.
  • Further research may explore the role of STAG1 and CUL3 interactions in OSCC.

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