Literature DB >> 12973668

High mobility group protein HMGA1 expression in breast cancer reveals a positive correlation with tumour grade.

A M Flohr1, P Rogalla, U Bonk, B Puettmann, H Buerger, G Gohla, J Packeisen, W Wosniok, S Loeschke, J Bullerdiek.   

Abstract

Members of the HMGA protein (high mobility group protein A) family act as master switches of the chromatin structure by bending DNA and thus modulating the formation of transcription factor complexes of a number of target genes. Accordingly, HMGA proteins have been shown to be associated with the development and/or progression of a variety of benign and malignant tumours. Nevertheless, the HMGA1 expression studies published so far have not included primary breast cancer samples. In this study we have investigated the HMGA1 expression patterns in a series of 170 breast cancer samples by immunohistochemistry. We have found a strong variation in HMGA1 expression between the tumours. Based on an immunoreactive score (IRS) 14.1% of the tumour samples were scored to IRS 8-12 (strong positivity for HMGA1), 24.7% were scored to IRS 4-6 (moderate positivity), 25.3% were scored to IRS 1-3 (weak positivity), and 35.9% showed no positivity at all. Immunoreaction could be detected in all histological types of breast cancers analysed with the exception of invasive papillary and cribriform carcinoma. Statistical analysis revealed a strong correlation between tumour grade and HMGA1 expression (rs=0.3516, p<0.0001). Thus, the HMGA1 expression level can be considered a potential prognostic marker for breast cancer.

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Year:  2003        PMID: 12973668     DOI: 10.14670/HH-18.999

Source DB:  PubMed          Journal:  Histol Histopathol        ISSN: 0213-3911            Impact factor:   2.303


  22 in total

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Journal:  Expert Opin Ther Targets       Date:  2014-03-31       Impact factor: 6.902

Review 2.  High mobility group proteins and their post-translational modifications.

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Journal:  Biochim Biophys Acta       Date:  2008-05-10

Review 3.  High mobility group A: a novel biomarker and therapeutic target in pancreatic adenocarcinoma.

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Journal:  Surgeon       Date:  2009-10       Impact factor: 2.392

Review 4.  The High Mobility Group A1 (HMGA1) Transcriptome in Cancer and Development.

Authors:  T F Sumter; L Xian; T Huso; M Koo; Y-T Chang; T N Almasri; L Chia; C Inglis; D Reid; L M S Resar
Journal:  Curr Mol Med       Date:  2016       Impact factor: 2.222

5.  High-mobility group A1 proteins enhance the expression of the oncogenic miR-222 in lung cancer cells.

Authors:  Yunzhi Zhang; Teng Ma; Shuping Yang; Mingying Xia; Jing Xu; Haijia An; Yajun Yang; Shilin Li
Journal:  Mol Cell Biochem       Date:  2011-06-09       Impact factor: 3.396

6.  Knockdown of HMGA1 inhibits human breast cancer cell growth and metastasis in immunodeficient mice.

Authors:  Francescopaolo Di Cello; James Shin; Kirsten Harbom; Cory Brayton
Journal:  Biochem Biophys Res Commun       Date:  2013-03-29       Impact factor: 3.575

7.  The Wnt/β-catenin/T-cell factor 4 pathway up-regulates high-mobility group A1 expression in colon cancer.

Authors:  Bethany M Bush; Ashton T Brock; Jiayue A Deng; Ronald A Nelson; Takita Felder Sumter
Journal:  Cell Biochem Funct       Date:  2012-09-07       Impact factor: 3.685

8.  HMGA1 reprograms somatic cells into pluripotent stem cells by inducing stem cell transcriptional networks.

Authors:  Sandeep N Shah; Candace Kerr; Leslie Cope; Elias Zambidis; Cyndi Liu; Joelle Hillion; Amy Belton; David L Huso; Linda M S Resar
Journal:  PLoS One       Date:  2012-11-15       Impact factor: 3.240

9.  HMGA1: a master regulator of tumor progression in triple-negative breast cancer cells.

Authors:  Sandeep N Shah; Leslie Cope; Weijie Poh; Amy Belton; Sujayita Roy; C Conover Talbot; Saraswati Sukumar; David L Huso; Linda M S Resar
Journal:  PLoS One       Date:  2013-05-02       Impact factor: 3.240

10.  HMGA1 promotes metastatic processes in basal-like breast cancer regulating EMT and stemness.

Authors:  Silvia Pegoraro; Gloria Ros; Silvano Piazza; Roberta Sommaggio; Yari Ciani; Antonio Rosato; Riccardo Sgarra; Giannino Del Sal; Guidalberto Manfioletti
Journal:  Oncotarget       Date:  2013-08
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