KRAS variation and risk of endometriosis
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⤵ 18 in-corpus citations
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This study genotyped 30 single-nucleotide polymorphisms in the KRAS locus in 959 endometriosis cases and controls, finding no association with disease risk.
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Abstract
Endometriosis is a common gynaecological disease with symptoms of pelvic pain and infertility which affects 7-10% of women in their reproductive years. Activation of an oncogenic allele of Kirsten rat sarcoma viral oncogene homologue (KRAS) in the reproductive tract of mice resulted in the development of endometriosis. We hypothesized that variation in KRAS may influence risk of endometriosis in humans. Thirty tagSNPs spanning a region of 60.7 kb across the KRAS locus were genotyped using iPLEX chemistry on a MALDI-TOF MassARRAY platform in 959 endometriosis cases and 959 unrelated controls, and data were analysed for association with endometriosis. Genotypes were obtained for most individuals with a mean completion rate of 99.1%. We identified six haplotype blocks across the KRAS locus in our sample. There were no significant differences between cases and controls in the frequencies of individual single-nucleotide polymorphisms (SNPs) or haplotypes. We also developed a rapid method to screen for 11 common KRAS and BRAF mutations on the Sequenom MassARRAY system. The assay detected all mutations previously identified by direct sequencing in a panel of positive controls. No germline variants for KRAS or BRAF were detected. Our results demonstrate that any risk of endometriosis in women because of common variation in KRAS must be very small.
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Cited by (18)
- Neuropeptide S receptor 1 is a nonhormonal treatment target in endometriosis 2021
- Transcriptome meta-analysis reveals differences of immune profile between eutopic endometrium from stage I-II and III-IV endometriosis independently of hormonal milieu 2020
- Lack of an Association between a Polymorphism in the KRAS 3′ Untranslated Region (rs61764370) and Endometriosis in a Large European Case-Control Study 2019
- Distinguishing the progression of an endometrioma: Benign or malignant? 2018
- Endometriosis risk alleles at 1p36.12 act through inverse regulation of<i>CDC42</i>and<i>LINC00339</i> 2016
- Endometrial vezatin and its association with endometriosis risk 2016
- Functional evaluation of genetic variants associated with endometriosis near GREB1 2015
- Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis 2014
- Women with endometriosis have a higher DNA repair capacity and diminished breast cancer risk. 2013
- A polymorphism in a let‐7 microRNA binding site of KRAS in women with endometriosis 2012
- Evaluation of polymorphisms in predicted target sites for micro RNAs differentially expressed in endometriosis 2010
- The role of iron in the pathogenesis of endometriosis 2009
- Increased Mitogen-Activated Protein Kinase Kinase/Extracellularly Regulated Kinase Activity in Human Endometrial Stromal Fibroblasts of Women with Endometriosis Reduces 3′,5′-Cyclic Adenosine 5′-Monophosphate Inhibition of Cyclin D1 2009
- Common Variation in the CYP17A1 and IFIT1 Genes on Chromosome 10 Does Not Contribute to the Risk of Endometriosis 2008
- Functional genetic polymorphisms and female reproductive disorders: Part II--endometriosis 2008
- Polymorphisms in the vascular endothelial growth factor gene and the risk of familial endometriosis 2008
- Tubal and ovarian pathways to pelvic epithelial cancer: a pathological perspective 2008
- Genetic variation in tumour necrosis factor and lymphotoxin is not associated with endometriosis in an Australian sample 2007
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