Literature DB >> 21811762

Protein expression of the Ets transcription factor Elf-1 in breast cancer cells is negatively correlated with histological grading, but not with clinical outcome.

Alice Gerloff1, Angela Dittmer, Ilka Oerlecke, Hans-Jürgen Holzhausen, Jürgen Dittmer.   

Abstract

Several members of the Ets (E26 transformation specific) transcription factor family are involved in tumor progression, e.g. by activating matrix metalloproteases. Ets proteins share a unique DNA-binding domain, the Ets domain, which specifically recognizes GGAA/T-containing sequences common in many promoters. While the roles of quite a number of Ets proteins in carcinogenesis have been well established, little is known about the importance of the Ets protein Elf-1 (E74-like factor 1) in cancer. Herein, we analyzed the expression of Elf-1 in breast cancer. We found that, like T-cells, breast cancer cells express both the 80 and 98 kDa isoforms of the Elf-1 protein with the 98 kDa isoform only be present in the nucleus. Immunohistochemical analysis of 119 breast cancer biopsies showed anti-Elf-1 immunoreactivity exclusively in the nucleus. Elf-1 expression varied largely among the breast cancer samples showing a negative correlation with histological grading. However, no association of Elf-1 expression with clinical outcome was observed, even when sub-cohorts of patients who received either only adjuvant endocrine treatment or only chemotherapy were separately analyzed. These data suggest that Elf-1 may modulate breast cancer progression to some extent without having an impact on survival of breast cancer patients.

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Year:  2011        PMID: 21811762     DOI: 10.3892/or.2011.1409

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  8 in total

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Journal:  J Cell Mol Med       Date:  2020-05-05       Impact factor: 5.310

2.  Estrogen induces Vav1 expression in human breast cancer cells.

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Journal:  PLoS One       Date:  2014-06-06       Impact factor: 3.240

3.  A meta-analysis of multiple matched copy number and transcriptomics data sets for inferring gene regulatory relationships.

Authors:  Richard Newton; Lorenz Wernisch
Journal:  PLoS One       Date:  2014-08-22       Impact factor: 3.240

4.  Indirect regulation of TFPI-2 expression by miR-494 in breast cancer cells.

Authors:  Marianne S Andresen; Benedicte Stavik; Marit Sletten; Mari Tinholt; Per Morten Sandset; Nina Iversen; Grethe Skretting
Journal:  Sci Rep       Date:  2020-03-04       Impact factor: 4.379

5.  CTCF and EGR1 suppress breast cancer cell migration through transcriptional control of Nm23-H1.

Authors:  Ka Ming Wong; Jiaxing Song; Yung H Wong
Journal:  Sci Rep       Date:  2021-01-12       Impact factor: 4.379

6.  Application of the RBBP9 Serine Hydrolase Inhibitor, ML114, Decouples Human Pluripotent Stem Cell Proliferation and Differentiation.

Authors:  Seakcheng Lim; Rachel A Shparberg; Jens R Coorssen; Michael D O'Connor
Journal:  Int J Mol Sci       Date:  2020-11-26       Impact factor: 5.923

7.  Bioinformatics and Functional Analysis of a New Nuclear Localization Sequence of the Influenza A Virus Nucleoprotein.

Authors:  Nhan L T Nguyen; Nelly Panté
Journal:  Cells       Date:  2022-09-22       Impact factor: 7.666

8.  Expression of transmembrane protein 26 (TMEM26) in breast cancer and its association with drug response.

Authors:  Norbert Nass; Angela Dittmer; Vicky Hellwig; Theresia Lange; Johanna Mirjam Beyer; Benjamin Leyh; Atanas Ignatov; Christine Weiβenborn; Tove Kirkegaard; Anne E Lykkesfeldt; Thomas Kalinski; Jürgen Dittmer
Journal:  Oncotarget       Date:  2016-06-21
  8 in total

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