Literature DB >> 7931823

Studies of c-jun oncogene expression in human breast using a new monoclonal antibody, NCL-DK4.

D G Tiniakos1, L E Scott, I P Corbett, N H Piggott, C H Horne.   

Abstract

A new monoclonal antibody to human c-jun oncoprotein, designated NCL-DK4, has been produced. NCL-DK4 has been proved to be highly effective for use on formalin-fixed, paraffin-embedded tissues, enabling the study of c-jun expression at a cellular level in both normal and neoplastic human tissues. The expression of c-jun oncogene has been examined in normal, benign, and malignant breast tissues, and c-jun-specific immunoreactivity in carcinomas has been related to histological type, tumour grade, c-erbB-2, oestrogen receptor, progesterone receptor, and epidermal growth factor receptor expression. Normal and benign breast tissues showed c-jun-specific immunostaining, which was weaker and in fewer cells compared with the c-jun immunoreactivity observed in breast carcinomas. No relationship was found between the degree of immunostaining and the extent of proliferative changes in benign breast tissues. Ninety per cent of all breast carcinomas studied showed c-jun-specific nuclear staining. There were no statistically significant differences in the intensity of c-jun immunoreactivity among grade I, II, and III infiltrating ductal carcinomas. There was no significant relationship between c-jun oncoprotein expression and c-erbB-2, oestrogen, progesterone, and epidermal growth factor receptor immunoreactivity.

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Year:  1994        PMID: 7931823     DOI: 10.1002/path.1711720106

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  6 in total

1.  COP1 and GSK3β cooperate to promote c-Jun degradation and inhibit breast cancer cell tumorigenesis.

Authors:  Jing Shao; Yong Teng; Ravi Padia; Sungguan Hong; Hyangsoon Noh; Xiayang Xie; Jeff S Mumm; Zheng Dong; Han-Fei Ding; John Cowell; Jaejik Kim; Jiahuai Han; Shuang Huang
Journal:  Neoplasia       Date:  2013-09       Impact factor: 5.715

2.  c-Jun/AP-1 overexpression reprograms ERα signaling related to tamoxifen response in ERα-positive breast cancer.

Authors:  Huan He; Indranil Sinha; Rongrong Fan; Lars-Arne Haldosen; Feifei Yan; Chunyan Zhao; Karin Dahlman-Wright
Journal:  Oncogene       Date:  2018-02-22       Impact factor: 9.867

3.  JAB1/CSN5: a new player in cell cycle control and cancer.

Authors:  Terry J Shackleford; Francois X Claret
Journal:  Cell Div       Date:  2010-10-18       Impact factor: 5.130

Review 4.  Oestrogen and growth factor cross-talk and endocrine insensitivity and acquired resistance in breast cancer.

Authors:  R I Nicholson; J M Gee
Journal:  Br J Cancer       Date:  2000-02       Impact factor: 7.640

5.  p53 protein as a prognostic indicator in breast carcinoma: a comparison of four antibodies for immunohistochemistry.

Authors:  G M Horne; J J Anderson; D G Tiniakos; G G McIntosh; M D Thomas; B Angus; J A Henry; T W Lennard; C H Horne
Journal:  Br J Cancer       Date:  1996-01       Impact factor: 7.640

6.  Tristetraprolin induces cell cycle arrest in breast tumor cells through targeting AP-1/c-Jun and NF-κB pathway.

Authors:  Li Xu; Huan Ning; Ling Gu; Qinghong Wang; Wenbao Lu; Hui Peng; Weiguang Cui; Baoling Ying; Christina R Ross; Gerald M Wilson; Lin Wei; William S M Wold; Jianguo Liu
Journal:  Oncotarget       Date:  2015-12-08
  6 in total

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