XRCC3 and RAD51 Expression Are Associated with Clinical Factors in Breast Cancer

被引:27
作者
Hu, Jia [1 ,2 ]
Wang, Ning [2 ]
Wang, Ya-Jie [2 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Affiliated Hosp 1, Dept Oncol 2, Beijing, Peoples R China
[2] Second Mil Med Univ, Changhai Hosp, Dept Oncol, Shanghai, Peoples R China
来源
PLOS ONE | 2013年 / 8卷 / 08期
关键词
IONIZING-RADIATION; REPAIR; RECEPTOR; CELLS; CARCINOMA; SURVIVAL; GENE; EGFR; PROGESTERONE; METAANALYSIS;
D O I
10.1371/journal.pone.0072104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aims: XRCC3 and RAD51 are two important members in homologous recombination repair pathway. This study was performed to detect the expressions of these two molecules in breast cancer and explore their correlations with clinicopathological factors. Methods and Results: Immunohistochemistry was used to detect protein expressions of XRCC3 and RAD51 in 248 cases of breast cancer tissue and 78 cases of adjacent non-cancerous tissue. Data showed that expressions for both XRCC3 and RAD51 were significantly increased in breast cancer. High XRCC3 expression was associated with large tumor size and positive PR and HER2 status, while high RAD51 expression was associated with axillary lymph node metastasis and positive PR and HER2 status. The result of multivariate analysis demonstrated that HER2, PR and RAD51 were significantly association with XRCC3. And besides XRCC3, axillary lymph node metastasis and PR were significantly correlated with RAD51. Conclusions: XRCC3 and RAD51 were significantly associated with clinicopathological factors and they might play important roles in the development and progress of breast cancer.
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页数:6
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共 32 条
  • [21] The Effect of a DNA Repair Gene on Cellular Invasiveness: Xrcc3 Over-Expression in Breast Cancer Cells
    Martinez-Marignac, Veronica L.
    Rodrigue, Amelie
    Davidson, David
    Couillard, Martin
    Al-Moustafa, Ala-Eddin
    Abramovitz, Mark
    Foulkes, William D.
    Masson, Jean-Yves
    Aloyz, Raquel
    [J]. PLOS ONE, 2011, 6 (01):
  • [22] Breast cancer outcomes by steroid hormone receptor status assessed visually and by computer image analysis
    Mohammed, Zahra M. A.
    Edwards, Joanne
    Orange, Clare
    Mallon, Elizabeth
    Doughty, Julie C.
    McMillan, Donald C.
    Going, James J.
    [J]. HISTOPATHOLOGY, 2012, 61 (02) : 283 - 292
  • [23] Perturbation of sheep ovarian surface epithelial cells by ovulation: evidence for roles of progesterone and poly(ADP-ribose) polymerase in the restoration of DNA integrity
    Murdoch, WJ
    [J]. JOURNAL OF ENDOCRINOLOGY, 1998, 156 (03) : 503 - 508
  • [24] In tumor cells regulation of DNA double strand break repair through EGF receptor involves both NHEJ and HR and is independent of p53 and K-Ras status
    Myllynen, Laura
    Rieckmann, Thorsten
    Dahm-Daphi, Jochen
    Kasten-Pisula, Ulla
    Petersen, Cordula
    Dikomey, Ekkehard
    Kriegs, Matte
    [J]. RADIOTHERAPY AND ONCOLOGY, 2011, 101 (01) : 147 - 151
  • [25] XRCC3 5'-UTR and IVS5-14 polymorphisms and breast cancer susceptibility: a meta-analysis
    Qiu, Li-Xin
    Mao, Chen
    Yao, Lei
    Yu, Ke-Da
    Zhan, Ping
    Chen, Bo
    Liu, Hai-Guang
    Yuan, Hui
    Zhang, Jian
    Xue, Kai
    Hu, Xi-Chun
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 2010, 122 (02) : 489 - 493
  • [26] Links between DNA double strand break repair and breast cancer:: Accumulating evidence from both familial and nonfamilial cases
    Ralhan, Ranju
    Kaur, Jatinder
    Kreienberg, Rolf
    Wiesmueller, Lisa
    [J]. CANCER LETTERS, 2007, 248 (01) : 1 - 17
  • [27] Rad51 overexpression promotes alternative double-strand break repair pathways and genome instability
    Richardson, C
    Stark, JM
    Ommundsen, M
    Jasin, M
    [J]. ONCOGENE, 2004, 23 (02) : 546 - 553
  • [28] ErbB2 expression through heterodimerization with erbB1 is necessary for ionizing radiation- but not EGF-induced activation of Akt survival pathway
    Toulany, Mamoud
    Minjgee, Minjmaa
    Kehlbach, Rainer
    Chen, Jianyong
    Baumann, Michael
    Rodemann, H. Peter
    [J]. RADIOTHERAPY AND ONCOLOGY, 2010, 97 (02) : 338 - 345
  • [29] Ten genes for inherited breast cancer
    Walsh, Tom
    King, Mary-Claire
    [J]. CANCER CELL, 2007, 11 (02) : 103 - 105
  • [30] In vitro evidence for homologous recombinational repair in resistance to melphalan
    Wang, ZM
    Chen, ZP
    Xu, ZY
    Christodoulopoulos, G
    Bello, V
    Mohr, G
    Aloyz, R
    Panasci, LC
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (19) : 1473 - 1478