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
  • [1] Testing for erbB-2 by immunohistochemistry in breast cancer
    Allred, DC
    Swanson, PE
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2000, 113 (02) : 171 - 175
  • [2] Ang KK, 2002, CANCER RES, V62, P7350
  • [3] Altered expression of DNA double-strand break detection and repair proteins in breast carcinomas
    Angèle, S
    Treilleux, I
    Brémond, A
    Tanière, P
    Hall, J
    [J]. HISTOPATHOLOGY, 2003, 43 (04) : 347 - 353
  • [4] [Anonymous], NCCN CLIN PRACT GUID
  • [5] High RAD51 mRNA expression characterize estrogen receptor-positive/progesteron receptor-negative breast cancer and is associated with patient's outcome
    Barbano, Raffaela
    Copetti, Massimiliano
    Perrone, Giuseppe
    Pazienza, Valerio
    Muscarella, Lucia Anna
    Balsamo, Teresa
    Storlazzi, Clelia Tiziana
    Ripoli, Maria
    Rinaldi, Monica
    Valori, Vanna Maria
    Latiano, Tiziana Pia
    Maiello, Evaristo
    Stanziale, Pietro
    Carella, Massimo
    Mangia, Alessandra
    Pellegrini, Fabio
    Bisceglia, Michele
    Muda, Andrea Onetti
    Altomare, Vittorio
    Murgo, Roberto
    Fazio, Vito Michele
    Parrella, Paola
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2011, 129 (03) : 536 - 545
  • [6] Aberrations of the MRE11-RAD50-NBS1 DNA damage sensor complex in human breast cancer: MRE11 as a candidate familial cancer-predisposing gene
    Bartkova, Jirina
    Tommiska, Johanna
    Oplustilova, Lenka
    Aaltonen, Kirsimari
    Tamminen, Anitta
    Heikkinen, Tuomas
    Mistrik, Martin
    Aittomaki, Kristiina
    Blomqvist, Carl
    Heikkila, Paivi
    Lukas, Jiri
    Nevanlinna, Heli
    Bartek, Jiri
    [J]. MOLECULAR ONCOLOGY, 2008, 2 (04) : 296 - 316
  • [7] Studies on the inhibition of feline EGFR in squamous cell carcinoma Enhancement of radiosensitivity and rescue of resistance to small molecule inhibitors
    Bergkvist, Gura T.
    Argyle, David J.
    Pang, Lisa Y.
    Muirhead, Rhona
    Yool, Donald A.
    [J]. CANCER BIOLOGY & THERAPY, 2011, 11 (11) : 927 - 937
  • [8] Xrcc3 is required for assembly of Rad51 complexes in vivo
    Bishop, DK
    Ear, U
    Bhattacharyya, A
    Calderone, C
    Beckett, M
    Weichselbaum, RR
    Shinohara, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (34) : 21482 - 21488
  • [9] Cuatrecasas M, 2006, HISTOL HISTOPATHOL, V21, P149, DOI 10.14670/HH-21.149
  • [10] Pro-survival AKT and ERK signaling from EGFR and mutant EGFRvIII enhances DNA double-strand break repair in human glioma cells
    Golding, Sarah E.
    Morgan, Rhiannon N.
    Adams, Bret R.
    Hawkins, Amy J.
    Povirk, Lawrence F.
    Valerie, Kristoffer
    [J]. CANCER BIOLOGY & THERAPY, 2009, 8 (08) : 730 - 738