Literature DB >> 1627814

pS2 expression in primary breast carcinomas: relationship to clinical and histological features and survival.

A D Thor1, F C Koerner, S M Edgerton, W C Wood, M A Stracher, L H Schwartz.   

Abstract

pS2 protein expression has been reported to have prognostic significance in human breast carcinomas and to correlate with estrogen receptor positivity, although these findings have not been confirmed by all investigators. pS2 positivity was compared to various clinical and histologic parameters in a retrospective study of 290 patients (median follow-up 7.2 years) and significantly correlated with tumor grade and estrogen receptor content (p = 0.001 and p = 0.0007, respectively). Significant associations between pS2 positivity and lymph node metastases, T stage, histologic tumor type, and patient age were not observed. Univariate and multivariate analyses (controlling for estrogen receptor content, T and N stage) of the patient population at large showed that pS2 positivity was not predictive of disease-free or overall survival. Univariate analysis of lymph node negative patients demonstrated that both pS2 and estrogen receptor positivity were significantly associated with a better outcome. Multivariate analysis of these patients, however, showed that only estrogen receptor data had independent prognostic significance. This study suggests that immunohistochemical analysis for pS2 protein expression will not contribute additional prognostic information if the estrogen receptor content is known.

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Year:  1992        PMID: 1627814     DOI: 10.1007/bf01836957

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  31 in total

1.  The 5' flanking region of the human pS2 gene mediates its transcriptional activation by estrogen in MCF-7 cells.

Authors:  M Roberts; J Wallace; J M Jeltsch; M Berry
Journal:  Biochem Biophys Res Commun       Date:  1988-02-29       Impact factor: 3.575

2.  Characterization of the estrogen-induced pS2 protein secreted by the human breast cancer cell line MCF-7.

Authors:  A M Nunez; S Jakowlev; J P Briand; M Gaire; A Krust; M C Rio; P Chambon
Journal:  Endocrinology       Date:  1987-11       Impact factor: 4.736

3.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures.

Authors:  S M Hsu; L Raine; H Fanger
Journal:  J Histochem Cytochem       Date:  1981-04       Impact factor: 2.479

4.  Cloning of cDNA sequences of hormone-regulated genes from the MCF-7 human breast cancer cell line.

Authors:  P Masiakowski; R Breathnach; J Bloch; F Gannon; A Krust; P Chambon
Journal:  Nucleic Acids Res       Date:  1982-12-20       Impact factor: 16.971

5.  Purification of an estrogen-regulated breast cancer protein by monoclonal antibody affinity chromatography.

Authors:  D J Adams; H Hajj; K G Bitar; D P Edwards; W L McGuire
Journal:  Endocrinology       Date:  1983-07       Impact factor: 4.736

6.  Estrogen and progesterone receptors in breast cancer patients. Epidemiologic characteristics and survival differences.

Authors:  A M Ruder; F Lubin; Y Wax; A Geier; E Alfundary; A Chetrit
Journal:  Cancer       Date:  1989-07-01       Impact factor: 6.860

7.  Specific expression of the pS2 gene in subclasses of breast cancers in comparison with expression of the estrogen and progesterone receptors and the oncogene ERBB2.

Authors:  M C Rio; J P Bellocq; B Gairard; U B Rasmussen; A Krust; C Koehl; H Calderoli; V Schiff; R Renaud; P Chambon
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

Review 8.  Current status of estrogen and progesterone receptors in breast cancer.

Authors:  W L McGuire; K B Horwitz; O H Pearson; A Segaloff
Journal:  Cancer       Date:  1977-06       Impact factor: 6.860

9.  The prognostic role of progesterone receptors in human breast cancer.

Authors:  W L McGuire; G M Clark
Journal:  Semin Oncol       Date:  1983-12       Impact factor: 4.929

10.  pS2 expression and response to hormonal therapy in patients with advanced breast cancer.

Authors:  L H Schwartz; F C Koerner; S M Edgerton; J M Sawicka; M C Rio; J P Bellocq; P Chambon; A D Thor
Journal:  Cancer Res       Date:  1991-01-15       Impact factor: 12.701

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  7 in total

1.  Association of pS2 (TFF1) release with breast tumour proliferative rate: in vitro and in vivo studies.

Authors:  S J Reshkin; T Tedone; M Correale; A Mangia; V Casavola; A Paradiso
Journal:  Cell Prolif       Date:  1999 Apr-Jun       Impact factor: 6.831

2.  Production and comparison of mature single-domain 'trefoil' peptides pNR-2/pS2 Cys58 and pNR-2/pS2 Ser58.

Authors:  M P Chadwick; F E May; B R Westley
Journal:  Biochem J       Date:  1995-06-15       Impact factor: 3.857

3.  Immunohistochemical determination of pS2 in invasive breast carcinomas: a study on 942 cases.

Authors:  I Soubeyran; J Wafflart; F Bonichon; I de Mascarel; M Trojani; M Durand; A Avril; J M Coindre
Journal:  Breast Cancer Res Treat       Date:  1995-05       Impact factor: 4.872

4.  Differential expression of steroid receptors, hsp27, and pS2 in a series of drug resistant human breast tumor cell lines derived following exposure to antitumor drugs or to fractionated X-irradiation.

Authors:  R D Whelan; B T Hill
Journal:  Breast Cancer Res Treat       Date:  1993       Impact factor: 4.872

5.  pS2 and response to adjuvant hormone therapy in primary breast cancer.

Authors:  F Spyratos; C Andrieu; K Hacène; P Chambon; M C Rio
Journal:  Br J Cancer       Date:  1994-02       Impact factor: 7.640

6.  Relationship of PS2 with response to tamoxifen therapy in patients with recurrent breast cancer.

Authors:  J A Foekens; H Portengen; M P Look; W L van Putten; B Thirion; M Bontenbal; J G Klijn
Journal:  Br J Cancer       Date:  1994-12       Impact factor: 7.640

7.  Pathological and biological features of mammographically detected invasive breast carcinomas.

Authors:  R Rajakariar; R A Walker
Journal:  Br J Cancer       Date:  1995-01       Impact factor: 7.640

  7 in total

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