Eintrag weiter verarbeiten
author_facet Kelemen, Linda E.
Goodman, Marc T.
McGuire, Valerie
Rossing, Mary Anne
Webb, Penelope M.
Köbel, Martin
Anton-Culver, Hoda
Beesley, Jonathan
Berchuck, Andrew
Brar, Sony
Carney, Michael E.
Chang-Claude, Jenny
Chenevix-Trench, Georgia
Cramer, Daniel W.
Cunningham, Julie M.
DiCioccio, Richard A.
Doherty, Jennifer A.
Easton, Douglas F.
Fredericksen, Zachary S.
Fridley, Brooke L.
Gates, Margaret A.
Gayther, Simon A.
Gentry-Maharaj, Aleksandra
Høgdall, Estrid
Kjær, Susanne Krüger
Lurie, Galina
Menon, Usha
Moorman, Patricia G.
Moysich, Kirsten
Ness, Roberta B.
Palmieri, Rachel T.
Pearce, Celeste L.
Pharoah, Paul D.P.
Ramus, Susan J.
Song, Honglin
Stram, Daniel O.
Tworoger, Shelley S.
Van Den Berg, David
Vierkant, Robert A.
Wang-Gohrke, Shan
Whittemore, Alice S.
Wilkens, Lynne R.
Wu, Anna H.
Schildkraut, Joellen M.
Sellers, Thomas A.
Goode, Ellen L.
Kelemen, Linda E.
Goodman, Marc T.
McGuire, Valerie
Rossing, Mary Anne
Webb, Penelope M.
Köbel, Martin
Anton-Culver, Hoda
Beesley, Jonathan
Berchuck, Andrew
Brar, Sony
Carney, Michael E.
Chang-Claude, Jenny
Chenevix-Trench, Georgia
Cramer, Daniel W.
Cunningham, Julie M.
DiCioccio, Richard A.
Doherty, Jennifer A.
Easton, Douglas F.
Fredericksen, Zachary S.
Fridley, Brooke L.
Gates, Margaret A.
Gayther, Simon A.
Gentry-Maharaj, Aleksandra
Høgdall, Estrid
Kjær, Susanne Krüger
Lurie, Galina
Menon, Usha
Moorman, Patricia G.
Moysich, Kirsten
Ness, Roberta B.
Palmieri, Rachel T.
Pearce, Celeste L.
Pharoah, Paul D.P.
Ramus, Susan J.
Song, Honglin
Stram, Daniel O.
Tworoger, Shelley S.
Van Den Berg, David
Vierkant, Robert A.
Wang-Gohrke, Shan
Whittemore, Alice S.
Wilkens, Lynne R.
Wu, Anna H.
Schildkraut, Joellen M.
Sellers, Thomas A.
Goode, Ellen L.
author Kelemen, Linda E.
Goodman, Marc T.
McGuire, Valerie
Rossing, Mary Anne
Webb, Penelope M.
Köbel, Martin
Anton-Culver, Hoda
Beesley, Jonathan
Berchuck, Andrew
Brar, Sony
Carney, Michael E.
Chang-Claude, Jenny
Chenevix-Trench, Georgia
Cramer, Daniel W.
Cunningham, Julie M.
DiCioccio, Richard A.
Doherty, Jennifer A.
Easton, Douglas F.
Fredericksen, Zachary S.
Fridley, Brooke L.
Gates, Margaret A.
Gayther, Simon A.
Gentry-Maharaj, Aleksandra
Høgdall, Estrid
Kjær, Susanne Krüger
Lurie, Galina
Menon, Usha
Moorman, Patricia G.
Moysich, Kirsten
Ness, Roberta B.
Palmieri, Rachel T.
Pearce, Celeste L.
Pharoah, Paul D.P.
Ramus, Susan J.
Song, Honglin
Stram, Daniel O.
Tworoger, Shelley S.
Van Den Berg, David
Vierkant, Robert A.
Wang-Gohrke, Shan
Whittemore, Alice S.
Wilkens, Lynne R.
Wu, Anna H.
Schildkraut, Joellen M.
Sellers, Thomas A.
Goode, Ellen L.
spellingShingle Kelemen, Linda E.
Goodman, Marc T.
McGuire, Valerie
Rossing, Mary Anne
Webb, Penelope M.
Köbel, Martin
Anton-Culver, Hoda
Beesley, Jonathan
Berchuck, Andrew
Brar, Sony
Carney, Michael E.
Chang-Claude, Jenny
Chenevix-Trench, Georgia
Cramer, Daniel W.
Cunningham, Julie M.
DiCioccio, Richard A.
Doherty, Jennifer A.
Easton, Douglas F.
Fredericksen, Zachary S.
Fridley, Brooke L.
Gates, Margaret A.
Gayther, Simon A.
Gentry-Maharaj, Aleksandra
Høgdall, Estrid
Kjær, Susanne Krüger
Lurie, Galina
Menon, Usha
Moorman, Patricia G.
Moysich, Kirsten
Ness, Roberta B.
Palmieri, Rachel T.
Pearce, Celeste L.
Pharoah, Paul D.P.
Ramus, Susan J.
Song, Honglin
Stram, Daniel O.
Tworoger, Shelley S.
Van Den Berg, David
Vierkant, Robert A.
Wang-Gohrke, Shan
Whittemore, Alice S.
Wilkens, Lynne R.
Wu, Anna H.
Schildkraut, Joellen M.
Sellers, Thomas A.
Goode, Ellen L.
Cancer Epidemiology, Biomarkers & Prevention
Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
Oncology
Epidemiology
author_sort kelemen, linda e.
spelling Kelemen, Linda E. Goodman, Marc T. McGuire, Valerie Rossing, Mary Anne Webb, Penelope M. Köbel, Martin Anton-Culver, Hoda Beesley, Jonathan Berchuck, Andrew Brar, Sony Carney, Michael E. Chang-Claude, Jenny Chenevix-Trench, Georgia Cramer, Daniel W. Cunningham, Julie M. DiCioccio, Richard A. Doherty, Jennifer A. Easton, Douglas F. Fredericksen, Zachary S. Fridley, Brooke L. Gates, Margaret A. Gayther, Simon A. Gentry-Maharaj, Aleksandra Høgdall, Estrid Kjær, Susanne Krüger Lurie, Galina Menon, Usha Moorman, Patricia G. Moysich, Kirsten Ness, Roberta B. Palmieri, Rachel T. Pearce, Celeste L. Pharoah, Paul D.P. Ramus, Susan J. Song, Honglin Stram, Daniel O. Tworoger, Shelley S. Van Den Berg, David Vierkant, Robert A. Wang-Gohrke, Shan Whittemore, Alice S. Wilkens, Lynne R. Wu, Anna H. Schildkraut, Joellen M. Sellers, Thomas A. Goode, Ellen L. 1055-9965 1538-7755 American Association for Cancer Research (AACR) Oncology Epidemiology http://dx.doi.org/10.1158/1055-9965.epi-09-1317 <jats:title>Abstract</jats:title> <jats:p>Background: We previously reported the risks of ovarian carcinoma for common polymorphisms in one-carbon transfer genes. We sought to replicate associations for DPYD rs1801265, DNMT3A rs13420827, MTHFD1 rs1950902, MTHFS rs17284990, and TYMS rs495139 with risk of ovarian carcinoma overall and to use the large sample of assembled cases to investigate associations by histologic type.</jats:p> <jats:p>Methods: Associations were evaluated in the Ovarian Cancer Association Consortium, including 16 studies of 5,593 epithelial ovarian carcinoma cases and 9,962 controls of white non-Hispanic origin. Odds ratios (OR) and 95% confidence intervals (CI) were adjusted for age and study site.</jats:p> <jats:p>Results: The five polymorphisms were not associated with ovarian carcinoma overall (Ptrend &amp;gt; 0.13); however, associations for the minor allele at TYMS rs495139 were observed for carcinomas of mucinous type (OR, 1.19; 95% CI, 1.03-1.39; P = 0.02), clear cell type (OR, 0.86; 95% CI, 0.75-0.99; P = 0.04), and endometrioid type (OR, 0.90; 95% CI, 0.81-0.99; P = 0.04; Pheterogeneity = 0.001). Restriction to low-grade mucinous carcinomas further strengthened the association for the mucinous type (OR, 1.32; 95% CI, 1.07-1.62; P = 0.01). TYMS rs495139 was not associated with serous type (OR, 1.06; 95% CI, 1.00-1.13; P = 0.05).</jats:p> <jats:p>Conclusions: TYMS rs495139 may be associated with a differential risk of ovarian carcinoma types, indicating the importance of accurate histopathologic classification.</jats:p> <jats:p>Impact: Biomarkers that distinguish ovarian carcinoma types are few, and TYMS rs495139 may provide a novel clue to type etiology. Cancer Epidemiol Biomarkers Prev; 19(7); 1822–30. ©2010 AACR.</jats:p> Genetic Variation in <i>TYMS</i> in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium Cancer Epidemiology, Biomarkers & Prevention
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series Cancer Epidemiology, Biomarkers & Prevention
source_id 49
title Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_unstemmed Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_full Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_fullStr Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_full_unstemmed Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_short Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_sort genetic variation in <i>tyms</i> in the one-carbon transfer pathway is associated with ovarian carcinoma types in the ovarian cancer association consortium
topic Oncology
Epidemiology
url http://dx.doi.org/10.1158/1055-9965.epi-09-1317
publishDate 2010
physical 1822-1830
description <jats:title>Abstract</jats:title> <jats:p>Background: We previously reported the risks of ovarian carcinoma for common polymorphisms in one-carbon transfer genes. We sought to replicate associations for DPYD rs1801265, DNMT3A rs13420827, MTHFD1 rs1950902, MTHFS rs17284990, and TYMS rs495139 with risk of ovarian carcinoma overall and to use the large sample of assembled cases to investigate associations by histologic type.</jats:p> <jats:p>Methods: Associations were evaluated in the Ovarian Cancer Association Consortium, including 16 studies of 5,593 epithelial ovarian carcinoma cases and 9,962 controls of white non-Hispanic origin. Odds ratios (OR) and 95% confidence intervals (CI) were adjusted for age and study site.</jats:p> <jats:p>Results: The five polymorphisms were not associated with ovarian carcinoma overall (Ptrend &amp;gt; 0.13); however, associations for the minor allele at TYMS rs495139 were observed for carcinomas of mucinous type (OR, 1.19; 95% CI, 1.03-1.39; P = 0.02), clear cell type (OR, 0.86; 95% CI, 0.75-0.99; P = 0.04), and endometrioid type (OR, 0.90; 95% CI, 0.81-0.99; P = 0.04; Pheterogeneity = 0.001). Restriction to low-grade mucinous carcinomas further strengthened the association for the mucinous type (OR, 1.32; 95% CI, 1.07-1.62; P = 0.01). TYMS rs495139 was not associated with serous type (OR, 1.06; 95% CI, 1.00-1.13; P = 0.05).</jats:p> <jats:p>Conclusions: TYMS rs495139 may be associated with a differential risk of ovarian carcinoma types, indicating the importance of accurate histopathologic classification.</jats:p> <jats:p>Impact: Biomarkers that distinguish ovarian carcinoma types are few, and TYMS rs495139 may provide a novel clue to type etiology. Cancer Epidemiol Biomarkers Prev; 19(7); 1822–30. ©2010 AACR.</jats:p>
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author Kelemen, Linda E., Goodman, Marc T., McGuire, Valerie, Rossing, Mary Anne, Webb, Penelope M., Köbel, Martin, Anton-Culver, Hoda, Beesley, Jonathan, Berchuck, Andrew, Brar, Sony, Carney, Michael E., Chang-Claude, Jenny, Chenevix-Trench, Georgia, Cramer, Daniel W., Cunningham, Julie M., DiCioccio, Richard A., Doherty, Jennifer A., Easton, Douglas F., Fredericksen, Zachary S., Fridley, Brooke L., Gates, Margaret A., Gayther, Simon A., Gentry-Maharaj, Aleksandra, Høgdall, Estrid, Kjær, Susanne Krüger, Lurie, Galina, Menon, Usha, Moorman, Patricia G., Moysich, Kirsten, Ness, Roberta B., Palmieri, Rachel T., Pearce, Celeste L., Pharoah, Paul D.P., Ramus, Susan J., Song, Honglin, Stram, Daniel O., Tworoger, Shelley S., Van Den Berg, David, Vierkant, Robert A., Wang-Gohrke, Shan, Whittemore, Alice S., Wilkens, Lynne R., Wu, Anna H., Schildkraut, Joellen M., Sellers, Thomas A., Goode, Ellen L.
author_facet Kelemen, Linda E., Goodman, Marc T., McGuire, Valerie, Rossing, Mary Anne, Webb, Penelope M., Köbel, Martin, Anton-Culver, Hoda, Beesley, Jonathan, Berchuck, Andrew, Brar, Sony, Carney, Michael E., Chang-Claude, Jenny, Chenevix-Trench, Georgia, Cramer, Daniel W., Cunningham, Julie M., DiCioccio, Richard A., Doherty, Jennifer A., Easton, Douglas F., Fredericksen, Zachary S., Fridley, Brooke L., Gates, Margaret A., Gayther, Simon A., Gentry-Maharaj, Aleksandra, Høgdall, Estrid, Kjær, Susanne Krüger, Lurie, Galina, Menon, Usha, Moorman, Patricia G., Moysich, Kirsten, Ness, Roberta B., Palmieri, Rachel T., Pearce, Celeste L., Pharoah, Paul D.P., Ramus, Susan J., Song, Honglin, Stram, Daniel O., Tworoger, Shelley S., Van Den Berg, David, Vierkant, Robert A., Wang-Gohrke, Shan, Whittemore, Alice S., Wilkens, Lynne R., Wu, Anna H., Schildkraut, Joellen M., Sellers, Thomas A., Goode, Ellen L., Kelemen, Linda E., Goodman, Marc T., McGuire, Valerie, Rossing, Mary Anne, Webb, Penelope M., Köbel, Martin, Anton-Culver, Hoda, Beesley, Jonathan, Berchuck, Andrew, Brar, Sony, Carney, Michael E., Chang-Claude, Jenny, Chenevix-Trench, Georgia, Cramer, Daniel W., Cunningham, Julie M., DiCioccio, Richard A., Doherty, Jennifer A., Easton, Douglas F., Fredericksen, Zachary S., Fridley, Brooke L., Gates, Margaret A., Gayther, Simon A., Gentry-Maharaj, Aleksandra, Høgdall, Estrid, Kjær, Susanne Krüger, Lurie, Galina, Menon, Usha, Moorman, Patricia G., Moysich, Kirsten, Ness, Roberta B., Palmieri, Rachel T., Pearce, Celeste L., Pharoah, Paul D.P., Ramus, Susan J., Song, Honglin, Stram, Daniel O., Tworoger, Shelley S., Van Den Berg, David, Vierkant, Robert A., Wang-Gohrke, Shan, Whittemore, Alice S., Wilkens, Lynne R., Wu, Anna H., Schildkraut, Joellen M., Sellers, Thomas A., Goode, Ellen L.
author_sort kelemen, linda e.
container_issue 7
container_start_page 1822
container_title Cancer Epidemiology, Biomarkers & Prevention
container_volume 19
description <jats:title>Abstract</jats:title> <jats:p>Background: We previously reported the risks of ovarian carcinoma for common polymorphisms in one-carbon transfer genes. We sought to replicate associations for DPYD rs1801265, DNMT3A rs13420827, MTHFD1 rs1950902, MTHFS rs17284990, and TYMS rs495139 with risk of ovarian carcinoma overall and to use the large sample of assembled cases to investigate associations by histologic type.</jats:p> <jats:p>Methods: Associations were evaluated in the Ovarian Cancer Association Consortium, including 16 studies of 5,593 epithelial ovarian carcinoma cases and 9,962 controls of white non-Hispanic origin. Odds ratios (OR) and 95% confidence intervals (CI) were adjusted for age and study site.</jats:p> <jats:p>Results: The five polymorphisms were not associated with ovarian carcinoma overall (Ptrend &amp;gt; 0.13); however, associations for the minor allele at TYMS rs495139 were observed for carcinomas of mucinous type (OR, 1.19; 95% CI, 1.03-1.39; P = 0.02), clear cell type (OR, 0.86; 95% CI, 0.75-0.99; P = 0.04), and endometrioid type (OR, 0.90; 95% CI, 0.81-0.99; P = 0.04; Pheterogeneity = 0.001). Restriction to low-grade mucinous carcinomas further strengthened the association for the mucinous type (OR, 1.32; 95% CI, 1.07-1.62; P = 0.01). TYMS rs495139 was not associated with serous type (OR, 1.06; 95% CI, 1.00-1.13; P = 0.05).</jats:p> <jats:p>Conclusions: TYMS rs495139 may be associated with a differential risk of ovarian carcinoma types, indicating the importance of accurate histopathologic classification.</jats:p> <jats:p>Impact: Biomarkers that distinguish ovarian carcinoma types are few, and TYMS rs495139 may provide a novel clue to type etiology. Cancer Epidemiol Biomarkers Prev; 19(7); 1822–30. ©2010 AACR.</jats:p>
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imprint American Association for Cancer Research (AACR), 2010
imprint_str_mv American Association for Cancer Research (AACR), 2010
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spelling Kelemen, Linda E. Goodman, Marc T. McGuire, Valerie Rossing, Mary Anne Webb, Penelope M. Köbel, Martin Anton-Culver, Hoda Beesley, Jonathan Berchuck, Andrew Brar, Sony Carney, Michael E. Chang-Claude, Jenny Chenevix-Trench, Georgia Cramer, Daniel W. Cunningham, Julie M. DiCioccio, Richard A. Doherty, Jennifer A. Easton, Douglas F. Fredericksen, Zachary S. Fridley, Brooke L. Gates, Margaret A. Gayther, Simon A. Gentry-Maharaj, Aleksandra Høgdall, Estrid Kjær, Susanne Krüger Lurie, Galina Menon, Usha Moorman, Patricia G. Moysich, Kirsten Ness, Roberta B. Palmieri, Rachel T. Pearce, Celeste L. Pharoah, Paul D.P. Ramus, Susan J. Song, Honglin Stram, Daniel O. Tworoger, Shelley S. Van Den Berg, David Vierkant, Robert A. Wang-Gohrke, Shan Whittemore, Alice S. Wilkens, Lynne R. Wu, Anna H. Schildkraut, Joellen M. Sellers, Thomas A. Goode, Ellen L. 1055-9965 1538-7755 American Association for Cancer Research (AACR) Oncology Epidemiology http://dx.doi.org/10.1158/1055-9965.epi-09-1317 <jats:title>Abstract</jats:title> <jats:p>Background: We previously reported the risks of ovarian carcinoma for common polymorphisms in one-carbon transfer genes. We sought to replicate associations for DPYD rs1801265, DNMT3A rs13420827, MTHFD1 rs1950902, MTHFS rs17284990, and TYMS rs495139 with risk of ovarian carcinoma overall and to use the large sample of assembled cases to investigate associations by histologic type.</jats:p> <jats:p>Methods: Associations were evaluated in the Ovarian Cancer Association Consortium, including 16 studies of 5,593 epithelial ovarian carcinoma cases and 9,962 controls of white non-Hispanic origin. Odds ratios (OR) and 95% confidence intervals (CI) were adjusted for age and study site.</jats:p> <jats:p>Results: The five polymorphisms were not associated with ovarian carcinoma overall (Ptrend &amp;gt; 0.13); however, associations for the minor allele at TYMS rs495139 were observed for carcinomas of mucinous type (OR, 1.19; 95% CI, 1.03-1.39; P = 0.02), clear cell type (OR, 0.86; 95% CI, 0.75-0.99; P = 0.04), and endometrioid type (OR, 0.90; 95% CI, 0.81-0.99; P = 0.04; Pheterogeneity = 0.001). Restriction to low-grade mucinous carcinomas further strengthened the association for the mucinous type (OR, 1.32; 95% CI, 1.07-1.62; P = 0.01). TYMS rs495139 was not associated with serous type (OR, 1.06; 95% CI, 1.00-1.13; P = 0.05).</jats:p> <jats:p>Conclusions: TYMS rs495139 may be associated with a differential risk of ovarian carcinoma types, indicating the importance of accurate histopathologic classification.</jats:p> <jats:p>Impact: Biomarkers that distinguish ovarian carcinoma types are few, and TYMS rs495139 may provide a novel clue to type etiology. Cancer Epidemiol Biomarkers Prev; 19(7); 1822–30. ©2010 AACR.</jats:p> Genetic Variation in <i>TYMS</i> in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium Cancer Epidemiology, Biomarkers & Prevention
spellingShingle Kelemen, Linda E., Goodman, Marc T., McGuire, Valerie, Rossing, Mary Anne, Webb, Penelope M., Köbel, Martin, Anton-Culver, Hoda, Beesley, Jonathan, Berchuck, Andrew, Brar, Sony, Carney, Michael E., Chang-Claude, Jenny, Chenevix-Trench, Georgia, Cramer, Daniel W., Cunningham, Julie M., DiCioccio, Richard A., Doherty, Jennifer A., Easton, Douglas F., Fredericksen, Zachary S., Fridley, Brooke L., Gates, Margaret A., Gayther, Simon A., Gentry-Maharaj, Aleksandra, Høgdall, Estrid, Kjær, Susanne Krüger, Lurie, Galina, Menon, Usha, Moorman, Patricia G., Moysich, Kirsten, Ness, Roberta B., Palmieri, Rachel T., Pearce, Celeste L., Pharoah, Paul D.P., Ramus, Susan J., Song, Honglin, Stram, Daniel O., Tworoger, Shelley S., Van Den Berg, David, Vierkant, Robert A., Wang-Gohrke, Shan, Whittemore, Alice S., Wilkens, Lynne R., Wu, Anna H., Schildkraut, Joellen M., Sellers, Thomas A., Goode, Ellen L., Cancer Epidemiology, Biomarkers & Prevention, Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium, Oncology, Epidemiology
title Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_full Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_fullStr Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_full_unstemmed Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_short Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
title_sort genetic variation in <i>tyms</i> in the one-carbon transfer pathway is associated with ovarian carcinoma types in the ovarian cancer association consortium
title_unstemmed Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium
topic Oncology, Epidemiology
url http://dx.doi.org/10.1158/1055-9965.epi-09-1317