NUCLEAR EXPRESSION OF KU70/80 IS ASSOCIATED WITH CHEK2 GERMLINE MUTATIONS IN BREAST CANCER

被引:0
|
作者
Rosik, Jakub [1 ]
Machaj, Filip [1 ,2 ]
Bodnar, Daniel [1 ]
Hybiak, Jolanta [1 ]
Huzarski, Tomasz [3 ]
Cybulski, Cezary [3 ]
Lubinski, Jan [3 ]
Domagala, Wenancjusz [1 ]
Domagala, Pawel [1 ,4 ]
机构
[1] Pomeranian Med Univ, Dept Pathol, Szczecin, Poland
[2] Med Univ Warsaw, Dept Med Biol, Warsaw, Poland
[3] Pomeranian Med Univ, Dept Genet & Pathol, Szczecin, Poland
[4] Pomeranian Med Univ, Dept Pathol, 1 Unii Lubelskiej St, PL-71252 Szczecin, Poland
关键词
breast cancer; CHEK2; Ku70; 80; END-JOINING PATHWAY; DNA-REPAIR; IMMUNOHISTOCHEMICAL ANALYSIS; PROTEIN-KINASE; UP-REGULATION; KU; CHEK2; ESTROGEN; PKCS; RESISTANCE;
D O I
10.5114/PJP.2023.129518
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Ku70/80 protein inhibitors reduce the repair of DNA double-strand breaks via the Ku70/80 pathway, so they can be used to treat cancers with Ku70/80 over expression. Since the association of Ku70/80 with germline CHEK2 mutations in breast cancer is unknown, in this study we evaluated the expression of Ku70/80 in breast cancers with germline CHEK2 mutations.Immunohistochemistry with a Ku70/80 antibody on tissue microarrays from 225 CHEK2-associated breast cancers was used and automatically assessed with computerized image analysis.We report that the vast majority of breast cancers expressed high level of nuclear Ku70/80 and a small percentage of tumors (3.5%) were negative for Ku70/80 expression. There was a significant difference between the nuclear Ku70/80 expression in CHEK2-associated vs. CHEK2-non-associated breast cancers in all tumors (p = 0.009), and in the estrogen receptor (ER) positive subgroup of breast cancers (p = 0.03).This study is the first reporting an association of Ku70/80 expression with CHEK2 germline mutations in breast cancer. The results suggest that evaluation of Ku70/80 expression in breast cancer may improve the selection of breast cancer patients for Ku70/80 inhibitor therapy, and point to CHEK2-associated breast cancer and a subset of ER-positive breast cancer as potential suitable targets for such therapy.
引用
收藏
页码:75 / 81
页数:7
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