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 (...

Full description

Bibliographic Details
Main Authors: Antonsson, A. (Author), Gordon, S. (Author), Green, A.C (Author), Hughes, M.C (Author), Liyanage, U.E (Author), Rodriguez-Acevedo, A.J (Author), van der Pols, J. (Author)
Format: Article
Language:English
Published: BioMed Central Ltd 2022
Subjects:
BCC
SCC
Online Access:View Fulltext in Publisher
LEADER 02252nam a2200265Ia 4500
001 10.1186-s12885-022-09565-6
008 220706s2022 CNT 000 0 und d
020 |a 14712407 (ISSN) 
245 1 0 |a Associations of keratinocyte cancers with snp variants in the sonic hedgehog pathway 
260 0 |b BioMed Central Ltd  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1186/s12885-022-09565-6 
520 3 |a 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. © 2022, The Author(s). 
650 0 4 |a BCC 
650 0 4 |a Case–Control study 
650 0 4 |a Genetics 
650 0 4 |a SCC 
650 0 4 |a Sonic Hedgehog pathway 
700 1 0 |a Antonsson, A.  |e author 
700 1 0 |a Gordon, S.  |e author 
700 1 0 |a Green, A.C.  |e author 
700 1 0 |a Hughes, M.C.  |e author 
700 1 0 |a Liyanage, U.E.  |e author 
700 1 0 |a Rodriguez-Acevedo, A.J.  |e author 
700 1 0 |a van der Pols, J.  |e author 
773 |t BMC Cancer