AI Article Synopsis

  • - Cervical cancer is a leading cancer in women, mainly linked to HPV types 16 and 18, with a significant part of cases showing genetic diversity that may influence cancer progression.
  • - This study analyzed HPV16 and HPV18 genetic variations in 594 Brazilian women with invasive cervical cancer, identifying prevalent lineages before Brazil's public immunization program.
  • - Findings revealed that lineage A was most common for both HPV16 (in 217 women) and HPV18 (in 56 women), with HPV16 showing signs of recent variant expansion associated with cancer, unlike HPV18.

Article Abstract

Cervical cancer is the fourth most common cancer among women, and ∼70-80% of these cancers are associated with two human papillomavirus types: HPV16 and HPV18. Several studies have reported that intra-type diversity is associated with the progression of infection to invasive cancer. Herein, we report the genetic diversity of HPV16 and HPV18 in a cohort of 594 Brazilian women with invasive cervical cancer and describe the prevalence of lineages and intra-type diversity prior to the implementation of the public immunization program in Brazil. HPV detection and genotyping were performed using PCR, PGMY/GP primers, and DNA extracted from fresh tumors. The HPV16 (378 women) and HPV18 (80 women) lineages were identified by PCR and sequencing of the LCR and E6 fragments, followed by SNV comparison and phylogenetic analysis. In our cohort, was found a higher frequency of the lineage A (in 217 women), followed by lineage D (in 97 women) and lineages B and C (in 10 women each) for HPV16; and a higher frequency of lineage A (in 56 women) followed by lineage B (in 15 women) in HPV18. The genetic diversity of HPV16 indicated a recent expansion of specific variants or a selective advantage that is associated with invasive cancer; this pattern was not observed for HPV18.

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Source
http://dx.doi.org/10.1002/jmv.24458DOI Listing

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