Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Aug 7:8:762.
doi: 10.3389/fcell.2020.00762. eCollection 2020.

Cryptorchidism and Testicular Tumor: Comprehensive Analysis of Common Clinical Features and Search of SNVs in the KIT and AR Genes

Affiliations

Cryptorchidism and Testicular Tumor: Comprehensive Analysis of Common Clinical Features and Search of SNVs in the KIT and AR Genes

Daniel Adrian Landero-Huerta et al. Front Cell Dev Biol. .

Abstract

Allelic variants in genes implicated in the development of testicular germ cell tumor (TGCT) could be present in patients with cryptorchidism (CO). Currently; the mechanisms explaining this relationship are still unknown. In this study the common clinical features in patients with CO and TGCT and 6 variants of KIT and AR genes associated to TGCT were analyzed. Population analyzed included 328 individuals: 91 patients with CO; 79 with TGCT, 13 of them with previous CO diagnosis, and 158 healthy males. Of the 13 patients with TGCT and history of CO, one patient (7.7%) presented the heterozygous form of the variant rs121913507 and two patients (15.4%) presented homozygote genotype for the variant rs121913506 in KIT gene. Interestingly, the heterozygous form for the variant rs121913506 of KIT gene was identifying in all of 13 patients. The rs201934623, rs774171864, and rs12014709 variants of the AR gene did not show any clinical association. Our results strongly support that genetic component in CO could be conditioning for the development of TGCT. Notably, KIT gene variants might be determinants in the pathological association between TGCT and CO.

Keywords: AR; KIT; SNVs; isolated cryptorchidism; testicular germ cell tumor.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Agarwal S., Kazi J., Mohlin S., Påhlman S., Rönnstrand L. (2014). The activation loop tyrosine 823 is essential for the transforming capacity of the c-Kit oncogenic mutant D816V. Oncogene 34 4581–4590. 10.1038/onc.2014.383 - DOI - PubMed
    1. Banks K., Tuazon E., Berhane K., Koh C., De Filippo R., Chang A., et al. (2013). Cryptorchidism and testicular germ cell tumors: comprehensive meta-analysis reveals that association between these conditions diminished over time and is modified by clinical characteristics. Front. Endocrinol. 3:182. 10.3389/fendo.2012.00182 - DOI - PMC - PubMed
    1. Barrett J., Fry B., Maller J., Daly M. (2004). Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21 263–265. 10.1093/bioinformatics/bth457 - DOI - PubMed
    1. Berney D., Looijenga L., Idrees M., Oosterhuis J., Rajpert-De Meyts E., Ulbright T., et al. (2016). Germ cell neoplasiain situ(GCNIS): evolution of the current nomenclature for testicular pre-invasive germ cell malignancy. Histopathology 69 7–10. 10.1111/his.12958 - DOI - PubMed
    1. Dalgaard M., Weinhold N., Edsgärd D., Silver J., Pers T., Nielsen J., et al. (2011). A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation. J. Med. Genet. 49 58–65. 10.1136/jmedgenet-2011-100174 - DOI - PMC - PubMed