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The role of NFKB1/NFKBIA genetic variants in HPV infection: A cross-sectional cohort study.
Sena, Michelle Mota; Trugilo, Kleber Paiva; Okuyama, Nádia Calvo Martins; Pereira, Érica Romão; Cezar-Dos-Santos, Fernando; Ferreira, Rodolfo Sanches; Esposito, Aline; Pereira, Ana Paula Lombardi; d'Oliveira Couto-Filho, José; Watanabe, Maria Angelica Ehara; de Oliveira, Karen Brajão.
Afiliación
  • Sena MM; Laboratory of Molecular Genetics and Immunology, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, PR 445 Km 380 Celso Garcia Cid highway, Londrina, Paraná, Brazil.
  • Trugilo KP; Laboratory of Molecular Genetics and Immunology, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, PR 445 Km 380 Celso Garcia Cid highway, Londrina, Paraná, Brazil.
  • Okuyama NCM; Laboratory of Molecular Genetics and Immunology, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, PR 445 Km 380 Celso Garcia Cid highway, Londrina, Paraná, Brazil.
  • Pereira ÉR; Laboratory of Molecular Genetics and Immunology, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, PR 445 Km 380 Celso Garcia Cid highway, Londrina, Paraná, Brazil.
  • Cezar-Dos-Santos F; Laboratory of Molecular Genetics and Immunology, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, PR 445 Km 380 Celso Garcia Cid highway, Londrina, Paraná, Brazil.
  • Ferreira RS; Laboratory of Molecular Genetics and Immunology, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, PR 445 Km 380 Celso Garcia Cid highway, Londrina, Paraná, Brazil.
  • Esposito A; Laboratory of Molecular Genetics and Immunology, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, PR 445 Km 380 Celso Garcia Cid highway, Londrina, Paraná, Brazil.
  • Pereira APL; Laboratory of Molecular Genetics and Immunology, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, PR 445 Km 380 Celso Garcia Cid highway, Londrina, Paraná, Brazil.
  • d'Oliveira Couto-Filho J; Londrina Cancer Hospital, Londrina, 86.015-520, PR, Brazil; Department of Gynecology and Obstetrics, State University of Londrina, Londrina, PR, 86.057-970, Brazil. Electronic address: jcouto@sercomtel.com.br.
  • Watanabe MAE; Laboratory of Studies and Polymorphisms Analysis, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, PR 445 Km 380 Celso Garcia Cid highway, Londrina, Paraná, Brazil. Electronic address: maewatuel@gmail.com.
  • de Oliveira KB; Laboratory of Molecular Genetics and Immunology, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, PR 445 Km 380 Celso Garcia Cid highway, Londrina, Paraná, Brazil. Electronic address: karen.brajao@uel.br.
Exp Mol Pathol ; 124: 104716, 2022 02.
Article en En | MEDLINE | ID: mdl-34767808
ABSTRACT
Human Papillomavirus (HPV) is the most frequent etiological agent sexually transmitted. In the context of the immune response, NF-kB pathway plays an important role controlling the expression of several genes essential to cellular activity and structural and/or functional changes in components of this pathway can promote the development of several tumors. Thus, the study purpose was to evaluate the influence of NFKB1 rs28362491 and NFKBIA rs696 genetic variants on HPV infection and cervical lesions development. In this study 334 patients were recruited, of whom 48.8% (n = 163) were HPV infected, and considered our case group. HPV-DNA was detected by polymerase chain reaction (PCR) and the genetic variants were assessed in blood cells and tumor tissues paraffin embedded samples through restriction fragment length polymorphism analysis. Among women who were recruited for this study who were infected, 37.4% presented precursor lesions and 16.8% were diagnosed with cervical cancer (CC). The present study did not observe significant effects of the interaction between such genetic variants on HPV infection, nor on the development of lesions and progression to CC. Further studies will be important to investigate if under some circumstance the NFKB1 rs28362491 and NFKBIA rs696 genetic variants influence the progression of HPV-associated lesions.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Infecciones por Papillomavirus / Inhibidor NF-kappaB alfa Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Middle aged Idioma: En Revista: Exp Mol Pathol Año: 2022 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Asunto principal: Infecciones por Papillomavirus / Inhibidor NF-kappaB alfa Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Middle aged Idioma: En Revista: Exp Mol Pathol Año: 2022 Tipo del documento: Article País de afiliación: Brasil