Literature DB >> 16144914

Estrogen-responsive finger protein as a new potential biomarker for breast cancer.

Takashi Suzuki1, Tomohiko Urano, Tohru Tsukui, Kuniko Horie-Inoue, Takuya Moriya, Takanori Ishida, Masami Muramatsu, Yasuyoshi Ouchi, Hironobu Sasano, Satoshi Inoue.   

Abstract

PURPOSE: Estrogen-responsive finger protein (Efp) is a member of RING finger-B box-Coiled Coil family and is also a downstream target of estrogen receptor alpha. Previously, Efp was shown to mediate estrogen-induced cell growth, which suggests possible involvement in the development of human breast carcinomas. In this study, we examined expression of Efp in breast carcinoma tissues and correlated these findings with various clinicopathologic variables. EXPERIMENTAL
DESIGN: Thirty frozen specimens of breast carcinomas were used for immunohistochemistry and laser capture microdissection/real-time PCR of Efp. Immunohistochemistry for Efp was also done in 151 breast carcinoma specimens fixed with formalin and embedded in paraffin wax.
RESULTS: Efp immunoreactivity was detected in breast carcinoma cells and was significantly associated with the mRNA level (n = 30). Efp immunoreactivity was positively associated with lymph node status or estrogen receptor alpha status and negatively correlated with histologic grade or 14-3-3sigma immunoreactivity (n = 151). Moreover, Efp immunoreactivity was significantly correlated with poor prognosis of breast cancer patients, and multivariate analyses of disease-free survival and overall survival for 151 breast cancer patients showed that Efp immunoreactivity was the independent marker.
CONCLUSIONS: Our data suggest that Efp immunoreactivity is a significant prognostic factor in breast cancer patients. These findings may account for an oncogenic role of Efp in the tumor progression of breast carcinoma.

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Year:  2005        PMID: 16144914     DOI: 10.1158/1078-0432.CCR-05-0040

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  26 in total

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2.  Crystal structure of the TRIM25 B30.2 (PRYSPRY) domain: a key component of antiviral signalling.

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Review 3.  TRIMming p53's anticancer activity.

Authors:  S Elabd; G Meroni; C Blattner
Journal:  Oncogene       Date:  2016-02-22       Impact factor: 9.867

4.  Oestrogen causes ATBF1 protein degradation through the oestrogen-responsive E3 ubiquitin ligase EFP.

Authors:  Xue-Yuan Dong; Xiaoying Fu; Songqing Fan; Peng Guo; Dan Su; Jin-Tang Dong
Journal:  Biochem J       Date:  2012-06-15       Impact factor: 3.857

Review 5.  Novel RING E3 ubiquitin ligases in breast cancer.

Authors:  Angelika Burger; Yutaka Amemiya; Richard Kitching; Arun K Seth
Journal:  Neoplasia       Date:  2006-08       Impact factor: 5.715

6.  TRIM proteins and cancer.

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Journal:  Nat Rev Cancer       Date:  2011-10-07       Impact factor: 60.716

7.  Oestrogen causes degradation of KLF5 by inducing the E3 ubiquitin ligase EFP in ER-positive breast cancer cells.

Authors:  Ke-Wen Zhao; Deepa Sikriwal; Xueyuan Dong; Peng Guo; Xiaodong Sun; Jin-Tang Dong
Journal:  Biochem J       Date:  2011-07-15       Impact factor: 3.857

8.  Prognostic value of ISG15 mRNA level in drinkers with esophageal squamous cell cancers.

Authors:  Jun Tao; Ping Hua; Jing Wen; Yi Hu; Hong Yang; Xuan Xie
Journal:  Int J Clin Exp Pathol       Date:  2015-09-01

9.  TRIM25 enhances cell growth and cell survival by modulating p53 signals via interaction with G3BP2 in prostate cancer.

Authors:  Ken-Ichi Takayama; Takashi Suzuki; Tomoaki Tanaka; Tetsuya Fujimura; Satoru Takahashi; Tomohiko Urano; Kazuhiro Ikeda; Satoshi Inoue
Journal:  Oncogene       Date:  2018-01-30       Impact factor: 9.867

10.  The RNA-binding protein repertoire of embryonic stem cells.

Authors:  S Chul Kwon; Hyerim Yi; Katrin Eichelbaum; Sophia Föhr; Bernd Fischer; Kwon Tae You; Alfredo Castello; Jeroen Krijgsveld; Matthias W Hentze; V Narry Kim
Journal:  Nat Struct Mol Biol       Date:  2013-08-04       Impact factor: 15.369

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