Cargando…

Associations of keratinocyte cancers with snp variants in the sonic hedgehog pathway

BACKGROUND: Sonic Hedgehog (SHH) pathway dysregulation is implicated in basal cell carcinoma (BCC) development. To evaluate the possible wider role of SHH gene variants in skin carcinogenesis, we assessed associations of genes in the SHH pathway with lifetime development of any keratinocyte cancer (...

Descripción completa

Detalles Bibliográficos
Autores principales: Rodriguez-Acevedo, Astrid J., Antonsson, Annika, Liyanage, Upekha E., Hughes, Maria Celia, Gordon, Scott, van der Pols, Jolieke, Green, Adele C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063108/
https://www.ncbi.nlm.nih.gov/pubmed/35505292
http://dx.doi.org/10.1186/s12885-022-09565-6
_version_ 1784699097432719360
author Rodriguez-Acevedo, Astrid J.
Antonsson, Annika
Liyanage, Upekha E.
Hughes, Maria Celia
Gordon, Scott
van der Pols, Jolieke
Green, Adele C.
author_facet Rodriguez-Acevedo, Astrid J.
Antonsson, Annika
Liyanage, Upekha E.
Hughes, Maria Celia
Gordon, Scott
van der Pols, Jolieke
Green, Adele C.
author_sort Rodriguez-Acevedo, Astrid J.
collection PubMed
description BACKGROUND: Sonic Hedgehog (SHH) pathway dysregulation is implicated in basal cell carcinoma (BCC) development. To evaluate the possible wider role of SHH gene variants in skin carcinogenesis, we assessed associations of genes in the SHH pathway with lifetime development of any keratinocyte cancer (KC), and with developing either BCCs or squamous cell carcinomas (SCCs) exclusively, in a 25-year prospective, population-based study of 1,621 Australians. METHODS: We genotyped 795 unrelated adults with available blood samples: 311 cases with any KC (186 developing BCCs-only, 55 SCCs-only, 70 BCCs and SCCs) and 484 controls. We compared allele frequencies of 158 independent SNPs across 43 SHH genes between cases and controls, and performed a gene-based analysis. RESULTS: We found associations between SNP rs4848627 (GLI2) (related to DNA synthesis in keratinocytes) and development of any KC (OR = 1.53; 95% CI = 1.06–2.13, P < 0.01) and SCCs exclusively (OR = 2.12; 95%CI = 1.39–3.23, P < 0.01). SNP rs3217882 located in CCND2 was associated with exclusive BCC development (OR = 1.43, CI = 1.12–1.82, P < 0.01). The gene-based analysis suggested an association of PRKACG (protein kinase cAMP-activated catalytic subunit gamma) with any KC (P = 0.013). CONCLUSION: We conclude that variants located in genes in the SHH pathway may are involved in SCC as well as BCC development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09565-6.
format Online
Article
Text
id pubmed-9063108
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-90631082022-05-04 Associations of keratinocyte cancers with snp variants in the sonic hedgehog pathway Rodriguez-Acevedo, Astrid J. Antonsson, Annika Liyanage, Upekha E. Hughes, Maria Celia Gordon, Scott van der Pols, Jolieke Green, Adele C. BMC Cancer Research BACKGROUND: Sonic Hedgehog (SHH) pathway dysregulation is implicated in basal cell carcinoma (BCC) development. To evaluate the possible wider role of SHH gene variants in skin carcinogenesis, we assessed associations of genes in the SHH pathway with lifetime development of any keratinocyte cancer (KC), and with developing either BCCs or squamous cell carcinomas (SCCs) exclusively, in a 25-year prospective, population-based study of 1,621 Australians. METHODS: We genotyped 795 unrelated adults with available blood samples: 311 cases with any KC (186 developing BCCs-only, 55 SCCs-only, 70 BCCs and SCCs) and 484 controls. We compared allele frequencies of 158 independent SNPs across 43 SHH genes between cases and controls, and performed a gene-based analysis. RESULTS: We found associations between SNP rs4848627 (GLI2) (related to DNA synthesis in keratinocytes) and development of any KC (OR = 1.53; 95% CI = 1.06–2.13, P < 0.01) and SCCs exclusively (OR = 2.12; 95%CI = 1.39–3.23, P < 0.01). SNP rs3217882 located in CCND2 was associated with exclusive BCC development (OR = 1.43, CI = 1.12–1.82, P < 0.01). The gene-based analysis suggested an association of PRKACG (protein kinase cAMP-activated catalytic subunit gamma) with any KC (P = 0.013). CONCLUSION: We conclude that variants located in genes in the SHH pathway may are involved in SCC as well as BCC development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09565-6. BioMed Central 2022-05-03 /pmc/articles/PMC9063108/ /pubmed/35505292 http://dx.doi.org/10.1186/s12885-022-09565-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Rodriguez-Acevedo, Astrid J.
Antonsson, Annika
Liyanage, Upekha E.
Hughes, Maria Celia
Gordon, Scott
van der Pols, Jolieke
Green, Adele C.
Associations of keratinocyte cancers with snp variants in the sonic hedgehog pathway
title Associations of keratinocyte cancers with snp variants in the sonic hedgehog pathway
title_full Associations of keratinocyte cancers with snp variants in the sonic hedgehog pathway
title_fullStr Associations of keratinocyte cancers with snp variants in the sonic hedgehog pathway
title_full_unstemmed Associations of keratinocyte cancers with snp variants in the sonic hedgehog pathway
title_short Associations of keratinocyte cancers with snp variants in the sonic hedgehog pathway
title_sort associations of keratinocyte cancers with snp variants in the sonic hedgehog pathway
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063108/
https://www.ncbi.nlm.nih.gov/pubmed/35505292
http://dx.doi.org/10.1186/s12885-022-09565-6
work_keys_str_mv AT rodriguezacevedoastridj associationsofkeratinocytecancerswithsnpvariantsinthesonichedgehogpathway
AT antonssonannika associationsofkeratinocytecancerswithsnpvariantsinthesonichedgehogpathway
AT liyanageupekhae associationsofkeratinocytecancerswithsnpvariantsinthesonichedgehogpathway
AT hughesmariacelia associationsofkeratinocytecancerswithsnpvariantsinthesonichedgehogpathway
AT gordonscott associationsofkeratinocytecancerswithsnpvariantsinthesonichedgehogpathway
AT vanderpolsjolieke associationsofkeratinocytecancerswithsnpvariantsinthesonichedgehogpathway
AT greenadelec associationsofkeratinocytecancerswithsnpvariantsinthesonichedgehogpathway