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WFRF:(Imyanitov Evgeny N)
 

Sökning: WFRF:(Imyanitov Evgeny N) > Inheritance of dele...

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  • Background: Most BRCA1 or BRCA2 mutation carriers have inherited a single (heterozygous) mutation. Transheterozygotes (TH) who have inherited deleterious mutations in both BRCA1 and BRCA2 are rare, and the consequences of transheterozygosity are poorly understood. Methods: From 32,295 female BRCA1/2 mutation carriers, we identified 93 TH (0.3 %). "Cases" were defined as TH, and "controls" were single mutations at BRCA1 (SH1) or BRCA2 (SH2). Matched SH1 "controls" carried a BRCA1 mutation found in the TH "case". Matched SH2 "controls" carried a BRCA2 mutation found in the TH "case". After matching the TH carriers with SH1 or SH2, 91 TH were matched to 9316 SH1, and 89 TH were matched to 3370 SH2. Results: The majority of TH (45.2 %) involved the three common Jewish mutations. TH were more likely than SH1 and SH2 women to have been ever diagnosed with breast cancer (BC; p = 0.002). TH were more likely to be diagnosed with ovarian cancer (OC) than SH2 (p = 0.017), but not SH1. Age at BC diagnosis was the same in TH vs. SH1 (p = 0.231), but was on average 4.5 years younger in TH than in SH2 (p < 0.001). BC in TH was more likely to be estrogen receptor (ER) positive (p = 0.010) or progesterone receptor (PR) positive (p = 0.013) than in SH1, but less likely to be ER positive (p < 0.001) or PR positive (p = 0.012) than SH2. Among 15 tumors from TH patients, there was no clear pattern of loss of heterozygosity (LOH) for BRCA1 or BRCA2 in either BC or OC. Conclusions: Our observations suggest that clinical TH phenotypes resemble SH1. However, TH breast tumor marker characteristics are phenotypically intermediate to SH1 and SH2.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

Nyckelord

BRCA1
BRCA2
Hereditary breast and ovarian cancer
Transheterozygosity

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Av författaren/redakt...
Rebbeck, Timothy ...
Friebel, Tara M.
Mitra, Nandita
Wan, Fei
Chen, Stephanie
Andrulis, Irene ...
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Apostolou, Paras ...
Arnold, Norbert
Arun, Banu K.
Barrowdale, Dani ...
Benitez, Javier
Berger, Raanan
Berthet, Pascali ...
Borg, Åke
Buys, Saundra S.
Caldes, Trinidad
Carter, Jonathan
Chiquette, Jocel ...
Claes, Kathleen ...
Couch, Fergus J.
Cybulski, Cezary
Daly, Mary B.
de la Hoya, Migu ...
Diez, Orland
Domchek, Susan M ...
Nathanson, Kathe ...
Durda, Katarzyna
Ellis, Steve
Evans, D. Gareth
Foretova, Lenka
Friedman, Eitan
Frost, Debra
Ganz, Patricia A ...
Garber, Judy
Glendon, Gord
Godwin, Andrew K ...
Greene, Mark H.
Gronwald, Jacek
Hahnen, Eric
Hallberg, Emily
Hamann, Ute
Hansen, Thomas V ...
Imyanitov, Evgen ...
Isaacs, Claudine
Jakubowska, Anna
Janavicius, Ramu ...
Jaworska-Bieniek ...
John, Esther M.
Karlan, Beth Y.
Kaufman, Bella
Kwong, Ava
Laitman, Yael
Lasset, Christin ...
Lazaro, Conxi
Lester, Jenny
Loman, Niklas
Lubinski, Jan
Manoukian, Siran ...
Mitchell, Gillia ...
Montagna, Marco
Neuhausen, Susan ...
Nevanlinna, Heli
Niederacher, Die ...
Nussbaum, Robert ...
Offit, Kenneth
Olah, Edith
Olopade, Olufunm ...
Park, Sue Kyung
Piedmonte, Mario ...
Radice, Paolo
Rappaport-Fuerha ...
Rookus, Matti A.
Seynaeve, Caroli ...
Simard, Jacques
Singer, Christia ...
Soucy, Penny
Southey, Melissa
Stoppa-Lyonnet, ...
Sukiennicki, Grz ...
Szabo, Csilla I.
Tancredi, Mariel ...
Teixeira, Manuel ...
Teo, Soo Hwang
Terry, Mary Beth
Thomassen, Mads
Tihomirova, Laim ...
Tischkowitz, Mar ...
Toland, Amanda E ...
Toloczko-Grabare ...
Tung, Nadine
van Rensburg, El ...
Villano, Danylo
Wang-Gohrke, Sha ...
Wappenschmidt, B ...
Weitzel, Jeffrey ...
Zidan, Jamal
Zorn, Kristin K.
McGuffog, Lesley
Easton, Douglas
Chenevix-Trench, ...
Antoniou, Antoni ...
Ramus, Susan J.
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MEDICIN OCH HÄLSOVETENSKAP
MEDICIN OCH HÄLS ...
och Klinisk medicin
och Cancer och onkol ...
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och Medicinsk geneti ...
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Lunds universitet

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