Abstract
Epithelial ovarian cancer (EOC) is the fifth leading cause of cancer mortality in American women. Normal ovarian physiology is intricately connected to small GTP binding proteins of the Ras superfamily (Ras, Rho, Rab, Arf, and Ran) which govern processes such as signal transduction, cell proliferation, cell motility, and vesicle transport. We hypothesized that common germline variation in genes encoding small GTPases is associated with EOC risk. We investigated 322 variants in 88 small GTPase genes in germline DNA of 18,736 EOC patients and 26,138 controls of European ancestry using a custom genotype array and logistic regression fitting log-additive models. Functional annotation was used to identify bio-features and expression quantitative trait loci that intersect with risk variants. One variant, ARHGEF10L (Rho guanine nucleotide exchange factor 10 like) rs2256787, was associated with increased endometrioid EOC risk (OR = 1.33, p = 4.46 x 10−6). Other variants of interest included another in ARHGEF10L, rs10788679, which was associated with invasive serous EOC risk (OR = 1.07, p = 0.00026) and two variants in AKAP6 (A-kinase anchoring protein 6) which were associated with risk of invasive EOC (rs1955513, OR = 0.90, p = 0.00033; rs927062, OR = 0.94, p = 0.00059). Functional annotation revealed that the two ARHGEF10L variants were located in super-enhancer regions and that AKAP6 rs927062 was associated with expression of GTPase gene ARHGAP5 (Rho GTPase activating protein 5). Inherited variants in ARHGEF10L and AKAP6, with potential transcriptional regulatory function and association with EOC risk, warrant investigation in independent EOC study populations.
Original language | English (US) |
---|---|
Article number | e0197561 |
Journal | PloS one |
Volume | 13 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2018 |
All Science Journal Classification (ASJC) codes
- General
Access to Document
Other files and links
Fingerprint
Dive into the research topics of 'Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver
}
Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility. / Earp, Madalene; Tyrer, Jonathan P.; Winham, Stacey J.; Lin, Hui Yi; Chornokur, Ganna; Dennis, Joe; Aben, Katja K.H.; Anton-Culver, Hoda; Antonenkova, Natalia; Bandera, Elisa V.; Bean, Yukie T.; Beckmann, Matthias W.; Bjorge, Line; Bogdanova, Natalia; Brinton, Louise A.; Brooks-Wilson, Angela; Bruinsma, Fiona; Bunker, Clareann H.; Butzow, Ralf; Campbell, Ian G.; Carty, Karen; Chang-Claude, Jenny; Cook, Linda S.; Cramer, Daniel W.; Cunningham, Julie M.; Cybulski, Cezary; Dansonka-Mieszkowska, Agnieszka; Despierre, Evelyn; Doherty, Jennifer A.; Dörk, Thilo; Du Bois, Andreas; Dürst, Matthias; Easton, Douglas F.; Eccles, Diana M.; Edwards, Robert P.; Ekici, Arif B.; Fasching, Peter A.; Fridley, Brooke L.; Gentry-Maharaj, Aleksandra; Giles, Graham G.; Glasspool, Rosalind; Goodman, Marc T.; Gronwald, Jacek; Harter, Philipp; Hein, Alexander; Heitz, Florian; Hildebrandt, Michelle A.T.; Hillemanns, Peter; Hogdall, Claus K.; Høgdall, Estrid; Hosono, Satoyo; Iversen, Edwin S.; Jakubowska, Anna; Jensen, Allan; Ji, Bu Tian; Jung, Audrey Y.; Karlan, Beth Y.; Kellar, Melissa; Kiemeney, Lambertus A.; Lim, Boon Kiong; Kjaer, Susanne K.; Krakstad, Camilla; Kupryjanczyk, Jolanta; Lambrechts, Diether; Lambrechts, Sandrina; Le, Nhu D.; Lele, Shashi; Lester, Jenny; Levine, Douglas A.; Li, Zheng; Liang, Dong; Lissowska, Jolanta; Lu, Karen; Lubinski, Jan; Lundvall, Lene; Massuger, Leon F.A.G.; Matsuo, Keitaro; McGuire, Valerie; McLaughlin, John R.; McNeish, Iain; Menon, Usha; Milne, Roger L.; Modugno, Francesmary; Moysich, Kirsten B.; Ness, Roberta B.; Nevanlinna, Heli; Odunsi, Kunle; Olson, Sara H.; Orlow, Irene; Orsulic, Sandra; Paul, James; Pejovic, Tanja; Pelttari, Liisa M.; Permuth, Jenny B.; Pike, Malcolm C.; Poole, Elizabeth M.; Rosen, Barry; Rossing, Mary Anne; Rothstein, Joseph H.; Runnebaum, Ingo B.; Rzepecka, Iwona K.; Schernhammer, Eva; Schwaab, Ira; Shu, Xiao Ou; Shvetsov, Yurii B.; Siddiqui, Nadeem; Sieh, Weiva; Song, Honglin; Southey, Melissa C.; Spiewankiewicz, Beata; Sucheston-Campbell, Lara; Tangen, Ingvild L.; Teo, Soo Hwang; Terry, Kathryn L.; Thompson, Pamela J.; Thomsen, Lotte; Tworoger, Shelley S.; Van Altena, Anne M.; Vergote, Ignace; Thomsen, Liv Cecilie Vestrheim; Vierkant, Robert A.; Walsh, Christine S.; Wang-Gohrke, Shan; Wentzensen, Nicolas; Whittemore, Alice S.; Wicklund, Kristine G.; Wilkens, Lynne R.; Woo, Yin Ling; Wu, Anna H.; Wu, Xifeng; Xiang, Yong Bing; Yang, Hannah; Zheng, Wei; Ziogas, Argyrios; Lee, Alice W.; Pearce, Celeste L.; Berchuck, Andrew; Schildkraut, Joellen M.; Ramus, Susan J.; Monteiro, Alvaro N.A.; Narod, Steven A.; Sellers, Thomas A.; Gayther, Simon A.; Kelemen, Linda E.; Chenevix-Trench, Georgia; Risch, Harvey A.; Pharoah, Paul D.P.; Goode, Ellen L.; Phelan, Catherine M.
In: PloS one, Vol. 13, No. 7, e0197561, 07.2018.Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility
AU - Earp, Madalene
AU - Tyrer, Jonathan P.
AU - Winham, Stacey J.
AU - Lin, Hui Yi
AU - Chornokur, Ganna
AU - Dennis, Joe
AU - Aben, Katja K.H.
AU - Anton-Culver, Hoda
AU - Antonenkova, Natalia
AU - Bandera, Elisa V.
AU - Bean, Yukie T.
AU - Beckmann, Matthias W.
AU - Bjorge, Line
AU - Bogdanova, Natalia
AU - Brinton, Louise A.
AU - Brooks-Wilson, Angela
AU - Bruinsma, Fiona
AU - Bunker, Clareann H.
AU - Butzow, Ralf
AU - Campbell, Ian G.
AU - Carty, Karen
AU - Chang-Claude, Jenny
AU - Cook, Linda S.
AU - Cramer, Daniel W.
AU - Cunningham, Julie M.
AU - Cybulski, Cezary
AU - Dansonka-Mieszkowska, Agnieszka
AU - Despierre, Evelyn
AU - Doherty, Jennifer A.
AU - Dörk, Thilo
AU - Du Bois, Andreas
AU - Dürst, Matthias
AU - Easton, Douglas F.
AU - Eccles, Diana M.
AU - Edwards, Robert P.
AU - Ekici, Arif B.
AU - Fasching, Peter A.
AU - Fridley, Brooke L.
AU - Gentry-Maharaj, Aleksandra
AU - Giles, Graham G.
AU - Glasspool, Rosalind
AU - Goodman, Marc T.
AU - Gronwald, Jacek
AU - Harter, Philipp
AU - Hein, Alexander
AU - Heitz, Florian
AU - Hildebrandt, Michelle A.T.
AU - Hillemanns, Peter
AU - Hogdall, Claus K.
AU - Høgdall, Estrid
AU - Hosono, Satoyo
AU - Iversen, Edwin S.
AU - Jakubowska, Anna
AU - Jensen, Allan
AU - Ji, Bu Tian
AU - Jung, Audrey Y.
AU - Karlan, Beth Y.
AU - Kellar, Melissa
AU - Kiemeney, Lambertus A.
AU - Lim, Boon Kiong
AU - Kjaer, Susanne K.
AU - Krakstad, Camilla
AU - Kupryjanczyk, Jolanta
AU - Lambrechts, Diether
AU - Lambrechts, Sandrina
AU - Le, Nhu D.
AU - Lele, Shashi
AU - Lester, Jenny
AU - Levine, Douglas A.
AU - Li, Zheng
AU - Liang, Dong
AU - Lissowska, Jolanta
AU - Lu, Karen
AU - Lubinski, Jan
AU - Lundvall, Lene
AU - Massuger, Leon F.A.G.
AU - Matsuo, Keitaro
AU - McGuire, Valerie
AU - McLaughlin, John R.
AU - McNeish, Iain
AU - Menon, Usha
AU - Milne, Roger L.
AU - Modugno, Francesmary
AU - Moysich, Kirsten B.
AU - Ness, Roberta B.
AU - Nevanlinna, Heli
AU - Odunsi, Kunle
AU - Olson, Sara H.
AU - Orlow, Irene
AU - Orsulic, Sandra
AU - Paul, James
AU - Pejovic, Tanja
AU - Pelttari, Liisa M.
AU - Permuth, Jenny B.
AU - Pike, Malcolm C.
AU - Poole, Elizabeth M.
AU - Rosen, Barry
AU - Rossing, Mary Anne
AU - Rothstein, Joseph H.
AU - Runnebaum, Ingo B.
AU - Rzepecka, Iwona K.
AU - Schernhammer, Eva
AU - Schwaab, Ira
AU - Shu, Xiao Ou
AU - Shvetsov, Yurii B.
AU - Siddiqui, Nadeem
AU - Sieh, Weiva
AU - Song, Honglin
AU - Southey, Melissa C.
AU - Spiewankiewicz, Beata
AU - Sucheston-Campbell, Lara
AU - Tangen, Ingvild L.
AU - Teo, Soo Hwang
AU - Terry, Kathryn L.
AU - Thompson, Pamela J.
AU - Thomsen, Lotte
AU - Tworoger, Shelley S.
AU - Van Altena, Anne M.
AU - Vergote, Ignace
AU - Thomsen, Liv Cecilie Vestrheim
AU - Vierkant, Robert A.
AU - Walsh, Christine S.
AU - Wang-Gohrke, Shan
AU - Wentzensen, Nicolas
AU - Whittemore, Alice S.
AU - Wicklund, Kristine G.
AU - Wilkens, Lynne R.
AU - Woo, Yin Ling
AU - Wu, Anna H.
AU - Wu, Xifeng
AU - Xiang, Yong Bing
AU - Yang, Hannah
AU - Zheng, Wei
AU - Ziogas, Argyrios
AU - Lee, Alice W.
AU - Pearce, Celeste L.
AU - Berchuck, Andrew
AU - Schildkraut, Joellen M.
AU - Ramus, Susan J.
AU - Monteiro, Alvaro N.A.
AU - Narod, Steven A.
AU - Sellers, Thomas A.
AU - Gayther, Simon A.
AU - Kelemen, Linda E.
AU - Chenevix-Trench, Georgia
AU - Risch, Harvey A.
AU - Pharoah, Paul D.P.
AU - Goode, Ellen L.
AU - Phelan, Catherine M.
N1 - Funding Information: Funding:Thescientificdevelopmentandfunding forthisprojectwerefundedbythefollowing:NIH R01CA-1491429(PhelanPI);theUSNational CancerInstitute(R01-CA076016);theCOGS projectisfundedthroughaEuropean Commission’sSeventhFrameworkProgramme grant(agreementnumber223175HEALTHF2 2009-223175);theGeneticAssociationsand Publisher Copyright: © This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
PY - 2018/7
Y1 - 2018/7
N2 - Epithelial ovarian cancer (EOC) is the fifth leading cause of cancer mortality in American women. Normal ovarian physiology is intricately connected to small GTP binding proteins of the Ras superfamily (Ras, Rho, Rab, Arf, and Ran) which govern processes such as signal transduction, cell proliferation, cell motility, and vesicle transport. We hypothesized that common germline variation in genes encoding small GTPases is associated with EOC risk. We investigated 322 variants in 88 small GTPase genes in germline DNA of 18,736 EOC patients and 26,138 controls of European ancestry using a custom genotype array and logistic regression fitting log-additive models. Functional annotation was used to identify bio-features and expression quantitative trait loci that intersect with risk variants. One variant, ARHGEF10L (Rho guanine nucleotide exchange factor 10 like) rs2256787, was associated with increased endometrioid EOC risk (OR = 1.33, p = 4.46 x 10−6). Other variants of interest included another in ARHGEF10L, rs10788679, which was associated with invasive serous EOC risk (OR = 1.07, p = 0.00026) and two variants in AKAP6 (A-kinase anchoring protein 6) which were associated with risk of invasive EOC (rs1955513, OR = 0.90, p = 0.00033; rs927062, OR = 0.94, p = 0.00059). Functional annotation revealed that the two ARHGEF10L variants were located in super-enhancer regions and that AKAP6 rs927062 was associated with expression of GTPase gene ARHGAP5 (Rho GTPase activating protein 5). Inherited variants in ARHGEF10L and AKAP6, with potential transcriptional regulatory function and association with EOC risk, warrant investigation in independent EOC study populations.
AB - Epithelial ovarian cancer (EOC) is the fifth leading cause of cancer mortality in American women. Normal ovarian physiology is intricately connected to small GTP binding proteins of the Ras superfamily (Ras, Rho, Rab, Arf, and Ran) which govern processes such as signal transduction, cell proliferation, cell motility, and vesicle transport. We hypothesized that common germline variation in genes encoding small GTPases is associated with EOC risk. We investigated 322 variants in 88 small GTPase genes in germline DNA of 18,736 EOC patients and 26,138 controls of European ancestry using a custom genotype array and logistic regression fitting log-additive models. Functional annotation was used to identify bio-features and expression quantitative trait loci that intersect with risk variants. One variant, ARHGEF10L (Rho guanine nucleotide exchange factor 10 like) rs2256787, was associated with increased endometrioid EOC risk (OR = 1.33, p = 4.46 x 10−6). Other variants of interest included another in ARHGEF10L, rs10788679, which was associated with invasive serous EOC risk (OR = 1.07, p = 0.00026) and two variants in AKAP6 (A-kinase anchoring protein 6) which were associated with risk of invasive EOC (rs1955513, OR = 0.90, p = 0.00033; rs927062, OR = 0.94, p = 0.00059). Functional annotation revealed that the two ARHGEF10L variants were located in super-enhancer regions and that AKAP6 rs927062 was associated with expression of GTPase gene ARHGAP5 (Rho GTPase activating protein 5). Inherited variants in ARHGEF10L and AKAP6, with potential transcriptional regulatory function and association with EOC risk, warrant investigation in independent EOC study populations.
UR - http://www.scopus.com/inward/record.url?scp=85049975237&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85049975237&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0197561
DO - 10.1371/journal.pone.0197561
M3 - Article
C2 - 29979793
AN - SCOPUS:85049975237
VL - 13
JO - PLoS One
JF - PLoS One
SN - 1932-6203
IS - 7
M1 - e0197561
ER -