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Pyknon-Containing Transcripts Are Downregulated in Colorectal Cancer Tumors, and Loss of PYK44 Is Associated With Worse Patient Outcome.
Evangelista, Adriane Feijó; de Menezes, Weder Pereira; Berardinelli, Gustavo Noriz; Dos Santos, Wellington; Scapulatempo-Neto, Cristovam; Guimarães, Denise Peixoto; Calin, George A; Reis, Rui Manuel.
Afiliação
  • Evangelista AF; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, Brazil.
  • de Menezes WP; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, Brazil.
  • Berardinelli GN; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, Brazil.
  • Dos Santos W; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, Brazil.
  • Scapulatempo-Neto C; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, Brazil.
  • Guimarães DP; Department of Pathology, Barretos Cancer Hospital, Barretos, Brazil.
  • Calin GA; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, Brazil.
  • Reis RM; Department of Endoscopy, Barretos Cancer Hospital, Barretos, Brazil.
Front Genet ; 11: 581454, 2020.
Article em En | MEDLINE | ID: mdl-33304384
Pyknons are specific human/primate-specific DNA motifs at least 16 nucleotides long that are repeated in blocks in intergenic and intronic regions of the genome and can be located in a new class of non-coding RNAs of variable length. Recent studies reported that pyknon deregulation could be involved in the carcinogenesis process, including colorectal cancer. We evaluated the expression profile of a set of 12 pyknons in a set of molecularly characterized colorectal cancer (CRC) patients. The pyknons (PYK10, PYK14, PYK17, PYK26, PYK27, PYK40, PYK41, PYK42, PYK43, PYK44, PYK83, and PYK90) expression was determined by qRT-PCR. A pilot analysis of 20 cases was performed, and consistent results were obtained for PYK10, PYK17, PYK42, PYK44, and PYK83. Further, the expression of the selected pyknons was evaluated in 73 CRC cases. Moreover, in 52 patients, we compared the expression profile in both tumor and normal tissues. All five pyknons analyzed showed significantly lower expression levels in the tumor compared to normal tissue. It was observed an association between expression of PYK10 with TP53 mutations (p = 0.029), PYK17 to histologic grade (p = 0.035), and PYK44 to clinical staging (p = 0.016). Moreover, levels of PYK44 were significantly associated with the patient's poor overall survival (p = 0.04). We reported the significant downregulation of pyknons motifs in tumor tissue compared with the normal counterpart, and the association of lower PYK44 expression with worse patient outcome. Further studies are needed to extend and validate these findings and determine the clinical-pathological impact.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article