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Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma.


ABSTRACT: BACKGROUND:Relative telomere length in peripheral blood leukocytes has been evaluated as a potential biomarker for renal cell carcinoma (RCC) risk in several studies, with conflicting findings. OBJECTIVE:We performed an analysis of genetic variants associated with leukocyte telomere length to assess the relationship between telomere length and RCC risk using Mendelian randomization, an approach unaffected by biases from temporal variability and reverse causation that might have affected earlier investigations. DESIGN, SETTING, AND PARTICIPANTS:Genotypes from nine telomere length-associated variants for 10 784 cases and 20 406 cancer-free controls from six genome-wide association studies (GWAS) of RCC were aggregated into a weighted genetic risk score (GRS) predictive of leukocyte telomere length. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS:Odds ratios (ORs) relating the GRS and RCC risk were computed in individual GWAS datasets and combined by meta-analysis. RESULTS AND LIMITATIONS:Longer genetically inferred telomere length was associated with an increased risk of RCC (OR=2.07 per predicted kilobase increase, 95% confidence interval [CI]:=1.70-2.53, p<0.0001). As a sensitivity analysis, we excluded two telomere length variants in linkage disequilibrium (R2>0.5) with GWAS-identified RCC risk variants (rs10936599 and rs9420907) from the telomere length GRS; despite this exclusion, a statistically significant association between the GRS and RCC risk persisted (OR=1.73, 95% CI=1.36-2.21, p<0.0001). Exploratory analyses for individual histologic subtypes suggested comparable associations with the telomere length GRS for clear cell (N=5573, OR=1.93, 95% CI=1.50-2.49, p<0.0001), papillary (N=573, OR=1.96, 95% CI=1.01-3.81, p=0.046), and chromophobe RCC (N=203, OR=2.37, 95% CI=0.78-7.17, p=0.13). CONCLUSIONS:Our investigation adds to the growing body of evidence indicating some aspect of longer telomere length is important for RCC risk. PATIENT SUMMARY:Telomeres are segments of DNA at chromosome ends that maintain chromosomal stability. Our study investigated the relationship between genetic variants associated with telomere length and renal cell carcinoma risk. We found evidence suggesting individuals with inherited predisposition to longer telomere length are at increased risk of developing renal cell carcinoma.

SUBMITTER: Machiela MJ 

PROVIDER: S-EPMC5641242 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature

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Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma.

Machiela Mitchell J MJ   Hofmann Jonathan N JN   Carreras-Torres Robert R   Brown Kevin M KM   Johansson Mattias M   Wang Zhaoming Z   Foll Matthieu M   Li Peng P   Rothman Nathaniel N   Savage Sharon A SA   Gaborieau Valerie V   McKay James D JD   Ye Yuanqing Y   Henrion Marc M   Bruinsma Fiona F   Jordan Susan S   Severi Gianluca G   Hveem Kristian K   Vatten Lars J LJ   Fletcher Tony T   Koppova Kvetoslava K   Larsson Susanna C SC   Wolk Alicja A   Banks Rosamonde E RE   Selby Peter J PJ   Easton Douglas F DF   Pharoah Paul P   Andreotti Gabriella G   Freeman Laura E Beane LEB   Koutros Stella S   Albanes Demetrius D   Mannisto Satu S   Weinstein Stephanie S   Clark Peter E PE   Edwards Todd E TE   Lipworth Loren L   Gapstur Susan M SM   Stevens Victoria L VL   Carol Hallie H   Freedman Matthew L ML   Pomerantz Mark M MM   Cho Eunyoung E   Kraft Peter P   Preston Mark A MA   Wilson Kathryn M KM   Gaziano J Michael JM   Sesso Howard S HS   Black Amanda A   Freedman Neal D ND   Huang Wen-Yi WY   Anema John G JG   Kahnoski Richard J RJ   Lane Brian R BR   Noyes Sabrina L SL   Petillo David D   Colli Leandro M LM   Sampson Joshua N JN   Besse Celine C   Blanche Helene H   Boland Anne A   Burdette Laurie L   Prokhortchouk Egor E   Skryabin Konstantin G KG   Yeager Meredith M   Mijuskovic Mirjana M   Ognjanovic Miodrag M   Foretova Lenka L   Holcatova Ivana I   Janout Vladimir V   Mates Dana D   Mukeriya Anush A   Rascu Stefan S   Zaridze David D   Bencko Vladimir V   Cybulski Cezary C   Fabianova Eleonora E   Jinga Viorel V   Lissowska Jolanta J   Lubinski Jan J   Navratilova Marie M   Rudnai Peter P   Szeszenia-Dabrowska Neonila N   Benhamou Simone S   Cancel-Tassin Geraldine G   Cussenot Olivier O   Bueno-de-Mesquita H Bas HB   Canzian Federico F   Duell Eric J EJ   Ljungberg Börje B   Sitaram Raviprakash T RT   Peters Ulrike U   White Emily E   Anderson Garnet L GL   Johnson Lisa L   Luo Juhua J   Buring Julie J   Lee I-Min IM   Chow Wong-Ho WH   Moore Lee E LE   Wood Christopher C   Eisen Timothy T   Larkin James J   Choueiri Toni K TK   Lathrop G Mark GM   Teh Bin Tean BT   Deleuze Jean-Francois JF   Wu Xifeng X   Houlston Richard S RS   Brennan Paul P   Chanock Stephen J SJ   Scelo Ghislaine G   Purdue Mark P MP  

European urology 20170807 5


<h4>Background</h4>Relative telomere length in peripheral blood leukocytes has been evaluated as a potential biomarker for renal cell carcinoma (RCC) risk in several studies, with conflicting findings.<h4>Objective</h4>We performed an analysis of genetic variants associated with leukocyte telomere length to assess the relationship between telomere length and RCC risk using Mendelian randomization, an approach unaffected by biases from temporal variability and reverse causation that might have af  ...[more]

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