Literature DB >> 19781322

Nuclear corepressor 1 expression predicts response to first-line endocrine therapy for breast cancer patients on relapse.

Zhen-huan Zhang1, Hiroko Yamashita, Tatsuya Toyama, Yutaka Yamamoto, Teru Kawasoe, Mutsuko Ibusuki, Saori Tomita, Hiroshi Sugiura, Shunzo Kobayashi, Yoshitaka Fujii, Hirotaka Iwase.   

Abstract

BACKGROUND: Estrogen receptor alpha (ER alpha) is the most important endocrine therapy responsiveness predictor for women with breast cancer. The accuracy of the prediction of the response to endocrine therapy was thought to be affected by involving the estrogen receptor coregulatory proteins and cross-talk between ER and other growth factor-signaling networks. Nuclear corepressor 1 (NCOR1) is one of the ER a transcription repressor. The objective of the study is to investigate the expression of NCOR1 at the protein level and pursue its predictive value for breast cancer endocrine therapy.
METHODS: In the present study, the level of expression of NCOR1 protein has been assessed by immunohistochemistry in 104 cases of invasive carcinoma of the breast. Associations between NCOR1 protein expression and different clinicopathological factors and survival were sought.
RESULTS: It was found that NCOR1 was expressed at significantly higher levels in responsive patients treated with endocrine therapy as first-line treatment on relapse. Responsive patients also had a significantly longer post-relapse survival and overall survival. No NCOR1 expression difference was found between patient by age, tumor size, lymph node status, different histological grade groups and human epidermal growth factor receptor 2 (HER2) status. Multivariate analysis showed that NCOR1 is an independent prognostic factor for over-all survival.
CONCLUSIONS: In breast cancer, NCOR1 protein expression level predicts response to endocrine therapy as first-line treatment for breast cancer patients on relapse and NCOR1 protein level assay may increase the accuracy in the endocrine treatment determination and, therefore, improving the patients survival.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19781322

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN: 0366-6999            Impact factor:   2.628


  4 in total

Review 1.  Minireview: The Link Between ERα Corepressors and Histone Deacetylases in Tamoxifen Resistance in Breast Cancer.

Authors:  Stéphanie Légaré; Mark Basik
Journal:  Mol Endocrinol       Date:  2016-07-20

2.  PDCD2 and NCoR1 as putative tumor suppressors in gastric gastrointestinal stromal tumors.

Authors:  Wei Wang; Xiao-Wen Song; Xian-Min Bu; Ning Zhang; Cheng-Hai Zhao
Journal:  Cell Oncol (Dordr)       Date:  2015-11-20       Impact factor: 6.730

Review 3.  The interaction between ER and NFκB in resistance to endocrine therapy.

Authors:  Leen Sas; Filip Lardon; Peter B Vermeulen; Jan Hauspy; Peter Van Dam; Patrick Pauwels; Luc Y Dirix; Steven J Van Laere
Journal:  Breast Cancer Res       Date:  2012-08-31       Impact factor: 6.466

4.  TNFα Enhances Tamoxifen Sensitivity through Dissociation of ERα-p53-NCOR1 Complexes in ERα-Positive Breast Cancer.

Authors:  Hyunhee Kim; Seung-Ho Park; Jangho Lee; Gi-Jun Sung; Ji-Hye Song; Sungmin Kwak; Ji-Hoon Jeong; Min-Jeong Kong; Jin-Taek Hwang; Hyo-Kyoung Choi; Kyung-Chul Choi
Journal:  Cancers (Basel)       Date:  2021-05-26       Impact factor: 6.639

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.