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Updated: Mar 19, 2026

Modeling Oral-Esophageal Squamous Cell Carcinoma in 3D Organoids
Published on: December 23, 2022
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.
Background:
Cohesin complex is responsible for sister chromatid cohesion. STAG1/STAG2 is part of the complex, which is regulated by PDS5B. Alterations in these genes were described in tumors. PDS5B is a negative regulator of cell proliferation. We aimed to assess molecular alterations in these genes in oral squamous cell carcinoma (OSCC) and predict their expression by the expression of 84 cell cycle genes. In addition, we investigated whether pds5b protein expression impacted ki-67 and p53 immunopositivity.
Methods:
We assessed loss of heterozygosity (LOH) at STAG1 and STAG2 loci in 15 OSCC using three polymorphic markers. Associations between the immunoexpression of pds5b and ki-67 and p53 were tested in 62 samples. Differences between transcriptional levels of STAG1, STAG2, and PDS5B between OSCC and normal oral mucosa (NM) were evaluated by qPCR. An 84 cell cycle genes qPCR array was carried with OSCC samples, and STAG1, STAG2, and PDS5B were independently used as response variables in multiple linear regression models.
Results:
Loss of heterozygosity in at least one marker was observed in three samples. pds5b, p53, and ki-67 were highly expressed, and no association was found between pds5b immunoexpression and ki-67 or p53 (P > 0.05). OSCC and NM showed similar transcriptional levels of STAG1, STAG2, and PDS5B. STAG1 and CUL3 expression seem to be related (P = 0.004).
Conclusions:
There is LOH at STAG1 and STAG2 loci in OSCC, but OSCC and NM showed similar transcriptional levels of STAG1, STAG2, and PDS5B. pds5b immunoexpression in OSCC was high, but it was not associated with proliferation cell index.
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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