Literature DB >> 8814701

Expression of FGFR2 BEK and K-SAM mRNA variants in normal and malignant human breast.

Y A Luqmani1, G S Bansal, C Mortimer, L Buluwela, R C Coombes.   

Abstract

The expression of mRNA encoding alternative forms of fibroblast growth factor receptor 2 (FGFR2) differing in the carboxy terminal half of their third immunoglobulin-like domain, was investigated in 77 human breast cancer tissues, 12 non-malignant breast biopsies and 29 cell lines, using a reverse transcriptase (RT) polymerase chain reaction (PCR) method. RNA from the two tissue groups yielded PCR product corresponding to both the BEK and the K-SAM form; amounts normalised to glyceraldehyde phosphate dehydrogenase product were similar in both groups. The level of either variant or of the total FGFR2 product was essentially unrelated to prognosis or clinical status except that patients with advanced clinical T staging had a higher proportion of BEK to K-SAM (P = 0.01). RNA from 1/2 normal breast derived and 8/10 breast cancer cell lines expressed exclusively or predominantly the K-SAM form; 2/10 had significant amounts of both BEK and K-SAM mRNA. Of 12 other epithelial lines, seven expressed mainly K-SAM mRNA, four expressed BEK and one was negative. Of five non-epithelial lines, one was negative, two expressed only BEK mRNA and two had significant amounts of both variants. We conclude that tissue levels of FGFR2 mRNA are unaltered in breast cancer extracts and that the splicing mechanism for this exon selection appears not to be significantly disrupted.

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Year:  1996        PMID: 8814701     DOI: 10.1016/0959-8049(95)00563-3

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  8 in total

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Authors:  Toshiyuki Ishiwata; Yoko Matsuda; Tetsushi Yamamoto; Eiji Uchida; Murray Korc; Zenya Naito
Journal:  Am J Pathol       Date:  2012-03-19       Impact factor: 4.307

3.  Histone-acetylated control of fibroblast growth factor receptor 2 intron 2 polymorphisms and isoform splicing in breast cancer.

Authors:  Xuegong Zhu; Sylvia L Asa; Shereen Ezzat
Journal:  Mol Endocrinol       Date:  2009-06-04

4.  PDGFRβ and FGFR2 mediate endothelial cell differentiation capability of triple negative breast carcinoma cells.

Authors:  Ilaria Plantamura; Patrizia Casalini; Erica Dugnani; Marianna Sasso; Elvira D'Ippolito; Monica Tortoreto; Matilde Cacciatore; Carla Guarnotta; Cristina Ghirelli; Isabella Barajon; Francesca Bianchi; Tiziana Triulzi; Roberto Agresti; Andrea Balsari; Manuela Campiglio; Claudio Tripodo; Marilena V Iorio; Elda Tagliabue
Journal:  Mol Oncol       Date:  2014-03-27       Impact factor: 6.603

5.  Allele-specific regulation of FGFR2 expression is cell type-dependent and may increase breast cancer risk through a paracrine stimulus involving FGF10.

Authors:  Petra E A Huijts; Minka van Dongen; Moniek C M de Goeij; Adrian J van Moolenbroek; Freek Blanken; Maaike P G Vreeswijk; Esther M de Kruijf; Wilma E Mesker; Erik W van Zwet; Rob A E M Tollenaar; Vincent T H B M Smit; Christi J van Asperen; Peter Devilee
Journal:  Breast Cancer Res       Date:  2011-07-18       Impact factor: 6.466

6.  Expression of keratinocyte growth factor and its receptor in human breast cancer.

Authors:  G S Bansal; H C Cox; S Marsh; J J Gomm; C Yiangou; Y Luqmani; R C Coombes; C L Johnston
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

7.  Comprehensive Analysis of Fibroblast Growth Factor Receptor (FGFR) Family Genes in Breast Cancer by Integrating Online Databases and Bioinformatics.

Authors:  Zhaoping Zhou; Baojin Wu; Xinjie Tang; Ronghu Ke; Qiang Zou
Journal:  Med Sci Monit       Date:  2020-05-08

8.  Real-time detection of mRNA splicing variants with specifically designed reverse-transcription loop-mediated isothermal amplification.

Authors:  Fengxia Su; Guanhao Wang; Jianing Ji; Pengbo Zhang; Fangfang Wang; Zhengping Li
Journal:  RSC Adv       Date:  2020-02-10       Impact factor: 4.036

  8 in total

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