↓ Skip to main content

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

Overview of attention for article published in JNCI: Journal of the National Cancer Institute, November 2015
Altmetric Badge

About this Attention Score

  • Good Attention Score compared to outputs of the same age (75th percentile)
  • Average Attention Score compared to outputs of the same age and source

Mentioned by

policy
1 policy source
twitter
4 X users

Readers on

mendeley
152 Mendeley
citeulike
1 CiteULike
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Article details
Title
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Published in
JNCI: Journal of the National Cancer Institute, November 2015
DOI 10.1093/jnci/djv315
Pubmed ID
Authors

Huong D. Meeks, Honglin Song, Kyriaki Michailidou, Manjeet K. Bolla, Joe Dennis, Qin Wang, Daniel Barrowdale, Debra Frost, EMBRACE, Lesley McGuffog, Steve Ellis, Bingjian Feng, Saundra S. Buys, John L. Hopper, Melissa C. Southey, Andrea Tesoriero, kConFab Investigators, Paul A. James, Fiona Bruinsma, Ian G. Campbell, Australia Ovarian Cancer Study Group, Annegien Broeks, Marjanka K. Schmidt, Frans B. L. Hogervorst, HEBON, Matthias W. Beckman, Peter A. Fasching, Olivia Fletcher, Nichola Johnson, Elinor J. Sawyer, Elio Riboli, Susana Banerjee, Usha Menon, Ian Tomlinson, Barbara Burwinkel, Ute Hamann, Frederik Marme, Anja Rudolph, Ramunas Janavicius, Laima Tihomirova, Nadine Tung, Judy Garber, Daniel Cramer, Kathryn L. Terry, Elizabeth M. Poole, Shelley S. Tworoger, Cecilia M. Dorfling, Elizabeth J. van Rensburg, Andrew K. Godwin, Pascal Guénel, Thérèse Truong, GEMO Study Collaborators, Dominique Stoppa-Lyonnet, Francesca Damiola, Sylvie Mazoyer, Olga M. Sinilnikova, Claudine Isaacs, Christine Maugard, Stig E. Bojesen, Henrik Flyger, Anne-Marie Gerdes, Thomas V. O. Hansen, Allen Jensen, Susanne K. Kjaer, Claus Hogdall, Estrid Hogdall, Inge Sokilde Pedersen, Mads Thomassen, Javier Benitez, Anna González-Neira, Ana Osorio, Miguel de la Hoya, Pedro Perez Segura, Orland Diez, Conxi Lazaro, Joan Brunet, Hoda Anton-Culver, Lee Eunjung, Esther M. John, Susan L. Neuhausen, Yuan Chun Ding, Danielle Castillo, Jeffrey N. Weitzel, Patricia A. Ganz, Robert L. Nussbaum, Salina B. Chan, Beth Y. Karlan, Jenny Lester, Anna Wu, Simon Gayther, Susan J. Ramus, Weiva Sieh, Alice S. Whittermore, Alvaro N. A. Monteiro, Catherine M. Phelan, Mary Beth Terry, Marion Piedmonte, Kenneth Offit, Mark Robson, Douglas Levine, Kirsten B. Moysich, Rikki Cannioto, Sara H. Olson, Mary B. Daly, Katherine L. Nathanson, Susan M. Domchek, Karen H. Lu, Dong Liang, Michelle A. T. Hildebrant, Roberta Ness, Francesmary Modugno, Leigh Pearce, Marc T. Goodman, Pamela J. Thompson, Hermann Brenner, Katja Butterbach, Alfons Meindl, Eric Hahnen, Barbara Wappenschmidt, Hiltrud Brauch, Thomas Brüning, Carl Blomqvist, Sofia Khan, Heli Nevanlinna, Liisa M. Pelttari, Kristiina Aittomäki, Ralf Butzow, Natalia V. Bogdanova, Thilo Dörk, Annika Lindblom, Sara Margolin, Johanna Rantala, Veli-Matti Kosma, Arto Mannermaa, Diether Lambrechts, Patrick Neven, Kathleen B. M. Claes, Tom Van Maerken, Jenny Chang-Claude, Dieter Flesch-Janys, Florian Heitz, Raymonda Varon-Mateeva, Paolo Peterlongo, Paolo Radice, Alessandra Viel, Monica Barile, Bernard Peissel, Siranoush Manoukian, Marco Montagna, Cristina Oliani, Ana Peixoto, Manuel R. Teixeira, Anita Collavoli, Emily Hallberg, Janet E. Olson, Ellen L. Goode, Steven N. Hart, Hermela Shimelis, Julie M. Cunningham, Graham G. Giles, Roger L. Milne, Sue Healey, Kathy Tucker, Christopher A. Haiman, Brian E. Henderson, Mark S. Goldberg, Marc Tischkowitz, Jacques Simard, Penny Soucy, Diana M. Eccles, Nhu Le, Anne-Lise Borresen-Dale, Vessela Kristensen, Helga B. Salvesen, Line Bjorge, Elisa V. Bandera, Harvey Risch, Wei Zheng, Alicia Beeghly-Fadiel, Hui Cai, Katri Pylkäs, Robert A. E. M. Tollenaar, Ans M. W. van der Ouweland, Irene L. Andrulis, Julia A. Knight, OCGN, Steven Narod, Peter Devilee, Robert Winqvist, Jonine Figueroa, Mark H. Greene, Phuong L., Jennifer T. Loud, Montserrat García-Closas, Minouk J. Schoemaker, Kamila Czene, Hatef Darabi, Iain McNeish, Nadeem Siddiquil, Rosalind Glasspool, Ava Kwong, Sue K. Park, Soo Hwang Teo, Sook-Yee Yoon, Keitaro Matsuo, Satoyo Hosono, Yin Ling Woo, Yu-Tang Gao, Lenka Foretova, Christian F. Singer, Christine Rappaport-Feurhauser, Eitan Friedman, Yael Laitman, Gad Rennert, Evgeny N. Imyanitov, Peter J. Hulick, Olufunmilayo I. Olopade, Leigha Senter, Edith Olah, Jennifer A. Doherty, Joellen Schildkraut, Linetta B. Koppert, Lambertus A. Kiemeney, Leon F. A. G. Massuger, Linda S. Cook, Tanja Pejovic, Jingmei Li, Ake Borg, Anna Öfverholm, Mary Anne Rossing, Nicolas Wentzensen, Karin Henriksson, Angela Cox, Simon S. Cross, Barbara J. Pasini, Mitul Shah, Maria Kabisch, Diana Torres, Anna Jakubowska, Jan Lubinski, Jacek Gronwald, Bjarni A. Agnarsson, Jolanta Kupryjanczyk, Joanna Moes-Sosnowska, Florentia Fostira, Irene Konstantopoulou, Susan Slager, Michael Jones, PRostate cancer AssoCiation group To Investigate Cancer Associated aLterations in the genome, Antonis C. Antoniou, Andrew Berchuck, Anthony Swerdlow, Georgia Chenevix-Trench, Alison M. Dunning, Paul D. P. Pharoah, Per Hall, Douglas F. Easton, Fergus J. Couch, Amanda B. Spurdle, David E. Goldgar

Abstract

The K3326X variant in BRCA2 (BRCA2*c.9976A>T; p.Lys3326*; rs11571833) has been found to be associated with small increased risks of breast cancer. However, it is not clear to what extent linkage disequilibrium with fully pathogenic mutations might account for this association. There is scant information about the effect of K3326X in other hormone-related cancers. Using weighted logistic regression, we analyzed data from the large iCOGS study including 76 637 cancer case patients and 83 796 control patients to estimate odds ratios (ORw) and 95% confidence intervals (CIs) for K3326X variant carriers in relation to breast, ovarian, and prostate cancer risks, with weights defined as probability of not having a pathogenic BRCA2 variant. Using Cox proportional hazards modeling, we also examined the associations of K3326X with breast and ovarian cancer risks among 7183 BRCA1 variant carriers. All statistical tests were two-sided. The K3326X variant was associated with breast (ORw = 1.28, 95% CI = 1.17 to 1.40, P = 5.9x10(-) (6)) and invasive ovarian cancer (ORw = 1.26, 95% CI = 1.10 to 1.43, P = 3.8x10(-3)). These associations were stronger for serous ovarian cancer and for estrogen receptor-negative breast cancer (ORw = 1.46, 95% CI = 1.2 to 1.70, P = 3.4x10(-5) and ORw = 1.50, 95% CI = 1.28 to 1.76, P = 4.1x10(-5), respectively). For BRCA1 mutation carriers, there was a statistically significant inverse association of the K3326X variant with risk of ovarian cancer (HR = 0.43, 95% CI = 0.22 to 0.84, P = .013) but no association with breast cancer. No association with prostate cancer was observed. Our study provides evidence that the K3326X variant is associated with risk of developing breast and ovarian cancers independent of other pathogenic variants in BRCA2. Further studies are needed to determine the biological mechanism of action responsible for these associations.

Login to access the Attention Digest and the Sentiment Analysis related to this output.

Timeline Attention over time Attention Score history
Login to access the full charts related to this output.
Activity
Login to access the full charts related to this output.
X Demographics

X Demographics

The data shown below were collected from the profiles of 4 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley demographics

Mendeley demographics

The data shown below were compiled from readership statistics for 152 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Login to view Mendeley reader trends over time.

Geographical breakdown

Geographical breakdown
Country Count As %
United Kingdom 1 <1%
Finland 1 <1%
Unknown 150 99%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Researcher 26 17%
Student > Ph. D. Student 16 11%
Professor 14 9%
Other 12 8%
Student > Bachelor 11 7%
Other 31 20%
Unknown 42 28%
Readers by discipline
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 40 26%
Medicine and Dentistry 32 21%
Agricultural and Biological Sciences 19 13%
Engineering 4 3%
Computer Science 3 2%
Other 10 7%
Unknown 44 29%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 6. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 18 July 2025.
All research outputs
#9,545,627
of 34,601,305 outputs
Outputs from JNCI: Journal of the National Cancer Institute
#5,042
of 9,923 outputs
Outputs of similar age
#108,448
of 440,705 outputs
Outputs of similar age from JNCI: Journal of the National Cancer Institute
#74
of 133 outputs
Altmetric has tracked 34,601,305 research outputs across all sources so far. This one has received more attention than most of these and is in the 72nd percentile.
So far Altmetric has tracked 9,923 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 21.3. This one is in the 48th percentile – i.e., 48% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 440,705 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 75% of its contemporaries.
We're also able to compare this research output to 133 others from the same source and published within six weeks on either side of this one. This one is in the 43rd percentile – i.e., 43% of its contemporaries scored the same or lower than it.