Sex-dependent development of Kras-induced anal squamous cell carcinoma in mice.

Anal squamous cell carcinoma (SCC) will be diagnosed in an estimated 9,080 adults in the United States this year, and rates have been rising over the last several decades. Most people that develop anal SCC have associated human papillomavirus (HPV) infection (~85-95%), with approximately 5-15% of an...

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Autores principales: Morgan T Walcheck, Kristina A Matkowskyj, Anne Turco, Simon Blaine-Sauer, Manabu Nukaya, Jessica Noel, Oline K Ronnekleiv, Sean M Ronnekleiv-Kelly
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Publicado: Public Library of Science (PLoS) 2021
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spelling oai:doaj.org-article:1802886f66cf438884e52de3683ceb342021-12-02T20:04:20ZSex-dependent development of Kras-induced anal squamous cell carcinoma in mice.1932-620310.1371/journal.pone.0259245https://doaj.org/article/1802886f66cf438884e52de3683ceb342021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0259245https://doaj.org/toc/1932-6203Anal squamous cell carcinoma (SCC) will be diagnosed in an estimated 9,080 adults in the United States this year, and rates have been rising over the last several decades. Most people that develop anal SCC have associated human papillomavirus (HPV) infection (~85-95%), with approximately 5-15% of anal SCC cases occurring in HPV-negative patients from unknown etiology. This study identified and characterized the Kras-driven, female sex hormone-dependent development of anal squamous cell carcinoma (SCC) in the LSL-KrasG12D; Pdx1-Cre (KC) mouse model that is not dependent on papillomavirus infection. One hundred percent of female KC mice develop anal SCC, while no male KC mice develop tumors. Both male and female KC anal tissue express Pdx1 and Cre-recombinase mRNA, and the activated mutant KrasG12D gene. Although the driver gene mutation KrasG12D is present in anus of both sexes, only female KC mice develop Kras-mutant induced anal SCC. To understand the sex-dependent differences, KC male mice were castrated and KC female mice were ovariectomized. Castrated KC males displayed an unchanged phenotype with no anal tumor formation. In contrast, ovariectomized KC females demonstrated a marked reduction in anal SCC development, with only 15% developing anal SCC. Finally, exogenous administration of estrogen rescued the tumor development in ovariectomized KC female mice and induced tumor development in castrated KC males. These results confirm that the anal SCC is estrogen mediated. The delineation of the role of female sex hormones in mediating mutant Kras to drive anal SCC pathogenesis highlights a subtype of anal SCC that is independent of papillomavirus infection. These findings may have clinical applicability for the papillomavirus-negative subset of anal SCC patients that typically respond poorly to standard of care chemoradiation.Morgan T WalcheckKristina A MatkowskyjAnne TurcoSimon Blaine-SauerManabu NukayaJessica NoelOline K RonnekleivSean M Ronnekleiv-KellyPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 11, p e0259245 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Morgan T Walcheck
Kristina A Matkowskyj
Anne Turco
Simon Blaine-Sauer
Manabu Nukaya
Jessica Noel
Oline K Ronnekleiv
Sean M Ronnekleiv-Kelly
Sex-dependent development of Kras-induced anal squamous cell carcinoma in mice.
description Anal squamous cell carcinoma (SCC) will be diagnosed in an estimated 9,080 adults in the United States this year, and rates have been rising over the last several decades. Most people that develop anal SCC have associated human papillomavirus (HPV) infection (~85-95%), with approximately 5-15% of anal SCC cases occurring in HPV-negative patients from unknown etiology. This study identified and characterized the Kras-driven, female sex hormone-dependent development of anal squamous cell carcinoma (SCC) in the LSL-KrasG12D; Pdx1-Cre (KC) mouse model that is not dependent on papillomavirus infection. One hundred percent of female KC mice develop anal SCC, while no male KC mice develop tumors. Both male and female KC anal tissue express Pdx1 and Cre-recombinase mRNA, and the activated mutant KrasG12D gene. Although the driver gene mutation KrasG12D is present in anus of both sexes, only female KC mice develop Kras-mutant induced anal SCC. To understand the sex-dependent differences, KC male mice were castrated and KC female mice were ovariectomized. Castrated KC males displayed an unchanged phenotype with no anal tumor formation. In contrast, ovariectomized KC females demonstrated a marked reduction in anal SCC development, with only 15% developing anal SCC. Finally, exogenous administration of estrogen rescued the tumor development in ovariectomized KC female mice and induced tumor development in castrated KC males. These results confirm that the anal SCC is estrogen mediated. The delineation of the role of female sex hormones in mediating mutant Kras to drive anal SCC pathogenesis highlights a subtype of anal SCC that is independent of papillomavirus infection. These findings may have clinical applicability for the papillomavirus-negative subset of anal SCC patients that typically respond poorly to standard of care chemoradiation.
format article
author Morgan T Walcheck
Kristina A Matkowskyj
Anne Turco
Simon Blaine-Sauer
Manabu Nukaya
Jessica Noel
Oline K Ronnekleiv
Sean M Ronnekleiv-Kelly
author_facet Morgan T Walcheck
Kristina A Matkowskyj
Anne Turco
Simon Blaine-Sauer
Manabu Nukaya
Jessica Noel
Oline K Ronnekleiv
Sean M Ronnekleiv-Kelly
author_sort Morgan T Walcheck
title Sex-dependent development of Kras-induced anal squamous cell carcinoma in mice.
title_short Sex-dependent development of Kras-induced anal squamous cell carcinoma in mice.
title_full Sex-dependent development of Kras-induced anal squamous cell carcinoma in mice.
title_fullStr Sex-dependent development of Kras-induced anal squamous cell carcinoma in mice.
title_full_unstemmed Sex-dependent development of Kras-induced anal squamous cell carcinoma in mice.
title_sort sex-dependent development of kras-induced anal squamous cell carcinoma in mice.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/1802886f66cf438884e52de3683ceb34
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