Perspectives on the role of breast cancer susceptibility gene in breast cancer

被引:4
作者
Wu, Nan [1 ]
Wei, Lijuan [1 ]
Li, Lijuan [1 ]
Li, Fangxuan [1 ]
Yu, Jinpu [3 ]
Liu, Juntian [1 ,2 ]
机构
[1] Tianjin Med Univ Canc Inst & Hosp, Canc Prevent Ctr, Natl Clin Res Ctr Canc, Key Lab Canc Prevent & Therapy, Tianjin 300060, Peoples R China
[2] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Dept Breast Canc 2, Key Lab Canc Prevent & Therapy, Tianjin 300060, Peoples R China
[3] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Key Lab Canc Prevent & Therapy, Mol Diagnost, Tianjin 300060, Peoples R China
关键词
Breast cancer; Breast cancer susceptibility gene 1/2; Immune cell infiltration; Immune checkpoint; Clinicopathologic features; Prognosis; LYMPHOCYTE-ACTIVATION GENE-3; TUMOR-INFILTRATING LYMPHOCYTES; T-CELLS; IMMUNE CHECKPOINT; BRCA2; MUTATIONS; PHASE-I; PD-1; OVARIAN; SAFETY; RISKS;
D O I
10.1007/s10147-021-02098-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Breast cancer susceptibility gene 1/2 can repair damaged DNA through homologous recombination. Besides, the local immune microenvironment of breast cancer is closely linked to the prognosis of patients. But the relationship of breast cancer susceptibility gene 1/2 expression and local immunosuppressive microenvironment in breast cancer is not clear. The aim of this study was to discuss the correlation between them. Methods The fresh primary breast tumors and paired normal tissues of 156 cases of breast cancer patients as well as peripheral blood of 156 cases among them in Tianjin Medical University Cancer Institute and Hospital from January 2014 to October 2018 were collected. The association between breast cancer susceptibility gene 1/2 germline mutation and immune status of microenvironment in situ was analyzed. Results The results indicated that the germline mutation of breast cancer susceptibility gene 1/2 was inconsistent with the breast cancer susceptibility gene 1/2 protein expression, and the proportion of immune cells in patients with negative expression of breast cancer susceptibility gene 1/2 protein was higher than patients with positive expression of breast cancer susceptibility gene 1/2 protein (p < 0.05). And the expression of programmed cell death protein 1, cytotoxic T-Lymphocyte Antigen 4, programmed death ligand-1 of CD3(+) T cells in patients with negative expression of breast cancer susceptibility gene 1/2 protein was higher than patients with positive expression of breast cancer susceptibility gene 1/2 protein (p < 0.05). The breast cancer susceptibility gene 1 protein expression was significantly correlated with family history of breast cancer patients (p = 0.006), local lymph node metastases (p = 0.001), and TNM staging (p <= 0.001). The breast cancer susceptibility gene 2 protein expression was significantly related to local lymph node metastases (p <= 0.001), III stage rate(p = 0.003) and molecular subtyping (p <= 0.001). Besides, the 5 years disease free survival was worse for G1 group and pathological III stage patients than other groups and other TNM stage patients. Conclusion In short, the immune therapy may be a potential therapy method for breast cancer patients with negative expression of breast cancer susceptibility gene 1/2 protein.
引用
收藏
页码:495 / 511
页数:17
相关论文
共 81 条
[1]   Signatures of mutational processes in human cancer [J].
Alexandrov, Ludmil B. ;
Nik-Zainal, Serena ;
Wedge, David C. ;
Aparicio, Samuel A. J. R. ;
Behjati, Sam ;
Biankin, Andrew V. ;
Bignell, Graham R. ;
Bolli, Niccolo ;
Borg, Ake ;
Borresen-Dale, Anne-Lise ;
Boyault, Sandrine ;
Burkhardt, Birgit ;
Butler, Adam P. ;
Caldas, Carlos ;
Davies, Helen R. ;
Desmedt, Christine ;
Eils, Roland ;
Eyfjord, Jorunn Erla ;
Foekens, John A. ;
Greaves, Mel ;
Hosoda, Fumie ;
Hutter, Barbara ;
Ilicic, Tomislav ;
Imbeaud, Sandrine ;
Imielinsk, Marcin ;
Jaeger, Natalie ;
Jones, David T. W. ;
Jones, David ;
Knappskog, Stian ;
Kool, Marcel ;
Lakhani, Sunil R. ;
Lopez-Otin, Carlos ;
Martin, Sancha ;
Munshi, Nikhil C. ;
Nakamura, Hiromi ;
Northcott, Paul A. ;
Pajic, Marina ;
Papaemmanuil, Elli ;
Paradiso, Angelo ;
Pearson, John V. ;
Puente, Xose S. ;
Raine, Keiran ;
Ramakrishna, Manasa ;
Richardson, Andrea L. ;
Richter, Julia ;
Rosenstiel, Philip ;
Schlesner, Matthias ;
Schumacher, Ton N. ;
Span, Paul N. ;
Teague, Jon W. .
NATURE, 2013, 500 (7463) :415-+
[2]   Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history:: A combined analysis of 22 studies [J].
Antoniou, A ;
Pharoah, PDP ;
Narod, S ;
Risch, HA ;
Eyfjord, JE ;
Hopper, JL ;
Loman, N ;
Olsson, H ;
Johannsson, O ;
Borg, Å ;
Pasini, B ;
Radice, P ;
Manoukian, S ;
Eccles, DM ;
Tang, N ;
Olah, E ;
Anton-Culver, H ;
Warner, E ;
Lubinski, J ;
Gronwald, J ;
Gorski, B ;
Tulinius, H ;
Thorlacius, S ;
Eerola, H ;
Nevanlinna, H ;
Syrjäkoski, K ;
Kallioniemi, OP ;
Thompson, D ;
Evans, C ;
Peto, J ;
Lalloo, F ;
Evans, DG ;
Easton, DF .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (05) :1117-1130
[3]  
Antoniou AC, 2014, NEW ENGL J MED, V371, P1651, DOI [10.1056/NEJMoa1400382, 10.1056/NEJMc1410673#SA1, 10.1056/NEJMc1410673]
[4]  
Ascierto PA, 2017, ANN ONCOL, V28
[5]   Genomics Comparisons across cancers [J].
Ashworth, Alan ;
Hudson, Thomas J. .
NATURE, 2013, 502 (7471) :306-307
[6]   The 2018 Nobel Prize in Physiology or Medicine: An exemplar of bench to bedside in immunology [J].
Ballas, Zuhair K. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2018, 142 (06) :1752-1753
[7]   BRCA in breast cancer: ESMO Clinical Practice Guidelines [J].
Balmana, J. ;
Diez, O. ;
Rubio, I. T. ;
Cardoso, F. .
ANNALS OF ONCOLOGY, 2011, 22 :vi31-vi34
[8]   Effect of BRCA germline mutations on breast cancer prognosis: A systematic review and meta-analysis [J].
Baretta, Zora ;
Mocellin, Simone ;
Goldin, Elena ;
Olopade, Olufunmilayo I. ;
Huo, Dezheng .
MEDICINE, 2016, 95 (40)
[9]   Prevalence and mutational determinants of high tumor mutation burden in breast cancer [J].
Barroso-Sousa, R. ;
Jain, E. ;
Cohen, O. ;
Kim, D. ;
Buendia-Buendia, J. ;
Winer, E. ;
Lin, N. ;
Tolaney, S. M. ;
Wagle, N. .
ANNALS OF ONCOLOGY, 2020, 31 (03) :387-394
[10]   MEK Inhibitor Selumetinib (AZD6244; ARRY-142886) Prevents Lung Metastasis in a Triple-Negative Breast Cancer Xenograft Model [J].
Bartholomeusz, Chandra ;
Xie, Xuemei ;
Pitner, Mary Kathryn ;
Kondo, Kimie ;
Dadbin, Ali ;
Lee, Jangsoon ;
Saso, Hitomi ;
Smith, Paul D. ;
Dalby, Kevin N. ;
Ueno, Naoto T. .
MOLECULAR CANCER THERAPEUTICS, 2015, 14 (12) :2773-2781