Abstract

It is suggested that HPV-18 variants from the A lineage have higher oncogenic potential compared to B variants. Some studies show uneven distribution of HPV-18 variants in cervical adenocarcinomas and squamous cell carcinomas. Regarding HPV-18 variants’ functions, the few studies reported focus on E6, and none were performed using natural host cells. Here, we immortalized primary human keratinocytes (PHKs) with E6/E7 of HPV-18 A1 and B1 sublineages and functionally characterized these cells. PHK18A1 reached immortalization significantly faster than PHK18B1 and formed a higher number of colonies in monolayer and 3D cultures. Moreover, PHK18A1 showed greater invasion ability and higher resistance to apoptosis induced by actinomycin-D. Nevertheless, no differences were observed regarding morphology, proliferation after immortalization, migration, or epithelial development in raft cultures. Noteworthy, our study highlights qualitative differences among HPV-18 A1 and B1 immortalized PHKs: in contrast to PHK18A1, which formed more compact colonies and spheroids of firmly grouped cells and tended to invade and migrate as clustered cells, morphologically, PHK18B1 colonies and spheroids were looser, and migration and invasion of single cells were observed. Although these observations may be relevant for the association of these variants with cervical cancer of different histological subtypes, further studies are warranted to elucidate the mechanisms behind these findings.

Highlights

  • Human papillomavirus (HPV) responds for virtually all cases of cervical cancer (CC).Worldwide, cervical squamous cell carcinomas (SCCs) are primarily associated with HPV16 infection (60%), while HPV-16 and -18 are prevalent in adenocarcinomas (ADCs) [1]

  • We characterized the biological properties of primary human keratinocytes (PHKs) immortalized by E6/E7 of HPV-18 A1 and B1 sublineage variants

  • Two distinct PHK pools were transduced with pLNSX E6/E7 of HPV-18 A1 or B1 sublineage variants

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Summary

Introduction

Human papillomavirus (HPV) responds for virtually all cases of cervical cancer (CC).Worldwide, cervical squamous cell carcinomas (SCCs) are primarily associated with HPV16 infection (60%), while HPV-16 and -18 are prevalent in adenocarcinomas (ADCs) [1]. Based on a fragment of the long control region (LCR), HPV-18 genetic variants were initially classified into three branches of phylogenetic and geographical relatedness: African (Af), Amerindian (As + AI or American Indian or East Asian), and European (E) [2]. The nomenclature of HPV-18 variants was revised, and these are categorized into variant lineages (1–2% sequence difference; designated by letters) and sublineages (0.5–1% sequence difference; designated by numbers) based on whole-genome sequencing. HPV-16 Asian American (AA) variants are clearly associated with a higher risk of cervical neoplasia and cancer development [5,6] and a higher oncogenic potential in vitro [7,8]

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