Journal article
Heterozygous deletion at the RLN1 locus in a family with testicular germ cell cancer identified by integrating copy number variation data with phenome and interactome information : Heterozygous deletion at the RLN1 locus
To search for disease‐related copy number variations (CNVs) in families with a high frequency of germ cell tumours (GCT), we analysed 16 individuals from four families by array comparative genomic hybridization (aCGH) and applied an integrative systems biology algorithm that prioritizes risk‐associated genes among loci targeted by CNVs.
The top‐ranked candidate, RLN1, encoding a Relaxin‐H1 peptide, although only detected in one of the families, was selected for further investigations. Validation of the CNV at the RLN1 locus was performed as an association study using qPCR with 106 sporadic testicular GCT patients and 200 healthy controls.
Observed CNV frequencies of 1.9% among cases and 1.5% amongst controls were not significantly different and this was further confirmed by CNV data extracted from a genome‐wide analysis of 189 cases and 380 controls, where similar frequencies of 2.2% were observed in both groups (p = 1). Immunohistochemistry for Relaxin‐H1 (RLN1), Relaxin‐H2 (RLN2) and their cognate receptor, RXFP1, detected one, and in some cases both, of the relaxins in Leydig cells, Sertoli cells and a subset of neoplastic germ cells, whereas the receptor was present in Leydig cells and spermatids.
Collectively, the findings show that a heterozygous loss at the RLN1 locus is not a genetic factor mediating high population‐wide risk for testicular germ cell tumour, but do not exclude a contribution of this aberration in some cases of cancer. The preliminary expression data suggest a possible role of the relaxin peptides in spermatogenesis and warrant further studies.
Language: | English |
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Year: | 2011 |
Pages: | e122-32 |
ISSN: | 13652605 , 01056263 , 13504908 and 01061607 |
Types: | Journal article |
DOI: | 10.1111/j.1365-2605.2011.01188.x |
ORCIDs: | Gupta, Ramneek |
Array-comparative genomic hybridization Familial testicular germ cell cancer Relaxin peptides Relaxin receptor SDG 3 - Good Health and Well-being Systems biology
Adolescent Adult Base Sequence Comparative Genomic Hybridization DNA Copy Number Variations Family Genetic Variation Genome-Wide Association Study Humans Male Middle Aged Neoplasms, Germ Cell and Embryonal Polymerase Chain Reaction RLN1 protein, human RLN2 protein, human RXFP1 protein, human Receptors, G-Protein-Coupled Receptors, Peptide Relaxin Sequence Deletion Testicular Neoplasms