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Prostate cancer risk SNP rs10993994 is a trans-eQTL for SNHG11 mediated through MSMB

Bicak, Mesude (author)
Icahn School of Medicine at Mount Sinai
Wang, Xing (author)
Icahn School of Medicine at Mount Sinai
Gao, Xiaoni (author)
Icahn School of Medicine at Mount Sinai,Memorial Sloan-Kettering Cancer Center
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Xu, Xing (author)
Memorial Sloan-Kettering Cancer Center
Väänänen, Riina Minna (author)
University of Turku
Taimen, Pekka (author)
Turku University Hospital
Lilja, Hans (author)
Lund University,Lunds universitet,Klinisk kemi, Malmö,Forskargrupper vid Lunds universitet,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Clinical Chemistry, Malmö,Lund University Research Groups,LUCC: Lund University Cancer Centre,Other Strong Research Environments,University of Oxford,Memorial Sloan-Kettering Cancer Center
Pettersson, Kim (author)
University of Turku
Klein, Robert J. (author)
Memorial Sloan-Kettering Cancer Center,Icahn School of Medicine at Mount Sinai
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 (creator_code:org_t)
2020-02-17
2020
English 11 s.
In: Human Molecular Genetics. - : Oxford University Press (OUP). - 0964-6906 .- 1460-2083. ; 29:10, s. 1581-1591
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • How genome-wide association studies-identified single-nucleotide polymorphisms (SNPs) affect remote genes remains unknown. Expression quantitative trait locus (eQTL) association meta-analysis on 496 prostate tumor and 602 normal prostate samples with 117 SNPs revealed novel cis-eQTLs and trans-eQTLs. Mediation testing and colocalization analysis demonstrate that MSMB is a cis-acting mediator for SNHG11 (P < 0.01). Removing rs10993994 in LNCaP cell lines by CRISPR/Cas9 editing shows that the C-allele corresponds with an over 100-fold increase in MSMB expression and 5-fold increase in SNHG11 compared with the T-allele. Colocalization analysis confirmed that the same set of SNPs associated with MSMB expression is associated with SNHG11 expression (posterior probability of shared variants is 66.6% in tumor and 91.4% in benign). These analyses further demonstrate variants driving MSMB expression differ in tumor and normal, suggesting regulatory network rewiring during tumorigenesis.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

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