Frontiers in Oncology (May 2021)

Dysregulation of Transcription Factor Networks Unveils Different Pathways in Human Papillomavirus 16-Positive Squamous Cell Carcinoma and Adenocarcinoma of the Uterine Cervix

  • Saloe Bispo,
  • Ticiana D. J. Farias,
  • Patricia Savio de Araujo-Souza,
  • Patricia Savio de Araujo-Souza,
  • Ricardo Cintra,
  • Hellen Geremias dos Santos,
  • Natasha Andressa Nogueira Jorge,
  • Natasha Andressa Nogueira Jorge,
  • Mauro Antônio Alves Castro,
  • Gabriel Wajnberg,
  • Gabriel Wajnberg,
  • Nicole de Miranda Scherer,
  • Maria Luiza Nogueira Dias Genta,
  • Jesus Paula Carvalho,
  • Luisa Lina Villa,
  • Luisa Lina Villa,
  • Laura Sichero,
  • Fabio Passetti,
  • Fabio Passetti

DOI
https://doi.org/10.3389/fonc.2021.626187
Journal volume & issue
Vol. 11

Abstract

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Squamous cell carcinoma (SCC) and adenocarcinoma (ADC) are the most common histological types of cervical cancer (CC). The worse prognosis of ADC cases highlights the need for better molecular characterization regarding differences between these CC types. RNA-Seq analysis of seven SCC and three ADC human papillomavirus 16-positive samples and the comparison with public data from non-tumoral human papillomavirus-negative cervical tissue samples revealed pathways exclusive to each histological type, such as the epithelial maintenance in SCC and the maturity-onset diabetes of the young (MODY) pathway in ADC. The transcriptional regulatory network analysis of cervical SCC samples unveiled a set of six transcription factor (TF) genes with the potential to positively regulate long non-coding RNA genes DSG1-AS1, CALML3-AS1, IGFL2-AS1, and TINCR. Additional analysis revealed a set of MODY TFs regulated in the sequence predicted to be repressed by miR-96-5p or miR-28-3p in ADC. These microRNAs were previously described to target LINC02381, which was predicted to be positively regulated by two MODY TFs upregulated in cervical ADC. Therefore, we hypothesize LINC02381 might act by decreasing the levels of miR-96-5p and miR-28-3p, promoting the MODY activation in cervical ADC. The novel TF networks here described should be explored for the development of more efficient diagnostic tools.

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