Docquier, France and Kita, Georgia-Xanthi and Farrar, Dawn and Jat, Parmjit and O'Hare, Michael and Chernukhin, Igor and Gretton, Svetlana and Mandal, Adhip and Alldridge, Louise and Klenova, Elena (2009) Decreased Poly(ADP-Ribosyl)ation of CTCF, a Transcription Factor, Is Associated with Breast Cancer Phenotype and Cell Proliferation. Clinical Cancer Research, 15 (18). pp. 5762-5771. DOI https://doi.org/10.1158/1078-0432.ccr-09-0329
Docquier, France and Kita, Georgia-Xanthi and Farrar, Dawn and Jat, Parmjit and O'Hare, Michael and Chernukhin, Igor and Gretton, Svetlana and Mandal, Adhip and Alldridge, Louise and Klenova, Elena (2009) Decreased Poly(ADP-Ribosyl)ation of CTCF, a Transcription Factor, Is Associated with Breast Cancer Phenotype and Cell Proliferation. Clinical Cancer Research, 15 (18). pp. 5762-5771. DOI https://doi.org/10.1158/1078-0432.ccr-09-0329
Docquier, France and Kita, Georgia-Xanthi and Farrar, Dawn and Jat, Parmjit and O'Hare, Michael and Chernukhin, Igor and Gretton, Svetlana and Mandal, Adhip and Alldridge, Louise and Klenova, Elena (2009) Decreased Poly(ADP-Ribosyl)ation of CTCF, a Transcription Factor, Is Associated with Breast Cancer Phenotype and Cell Proliferation. Clinical Cancer Research, 15 (18). pp. 5762-5771. DOI https://doi.org/10.1158/1078-0432.ccr-09-0329
Abstract
<jats:title>Abstract</jats:title> <jats:p>Purpose: There is compelling evidence of a relationship between poly(ADP-ribosyl)ation and tumorigenesis; however, much less is known about the role of specific targets of poly(ADP-ribosyl)ation in tumor development. Two forms of the multifunctional transcription factor, CTCF, were previously identified: a 130-kDa protein (CTCF-130), characteristic for cell lines, and a 180-kDa protein (CTCF-180), modified by poly(ADP-ribosyl)ation. This study was aimed to investigate differential poly(ADP-ribosyl)ation of CTCF in normal and tumor breast tissues.</jats:p> <jats:p>Experimental Design: Western blot analysis, mass spectrometry, and immunohistochemical and immunofluorescent stainings were used to characterize CTCF-130 and CTCF-180 in breast cell lines, primary cultures, and normal and tumor breast tissues. The immunoreactivity score was used for CTCF-130 quantification in tissues.</jats:p> <jats:p>Results: We discovered that only CTCF-180 is detected in the normal breast tissues, whereas both CTCF-130 and CTCF-180 are present in breast tumors. Using an antibody specific for CTCF-130, we observed that 87.7% of breast tumors were positive for CTCF-130. A negative correlation existed between the levels of CTCF-130, tumor stage, and tumor size. Significantly, a transition from CTCF-180 to CTCF-130 was discovered in primary cultures generated from normal breast tissues, indicating a link between CTCF-130 and proliferation. Conversely, the appearance of CTCF-180 was observed following growth arrest in breast cell lines.</jats:p> <jats:p>Conclusions: Collectively, our data suggest that the loss of CTCF poly(ADP-ribosyl)ation is associated with cell proliferation and breast tumor development. We propose the use of CTCF-130 as a marker for tumor breast cells and lower levels of CTCF-130 as an indicator of unfavorable prognosis. (Clin Cancer Res 2009;15(18):5762–71)</jats:p>
Item Type: | Article |
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Uncontrolled Keywords: | Tumor Cells, Cultured; Humans; Breast Neoplasms; Poly(ADP-ribose) Polymerases; Poly Adenosine Diphosphate Ribose; Repressor Proteins; Cell Proliferation; Phenotype; CCCTC-Binding Factor |
Subjects: | R Medicine > RC Internal medicine > RC0254 Neoplasms. Tumors. Oncology (including Cancer) |
Divisions: | Faculty of Science and Health Faculty of Science and Health > Life Sciences, School of |
SWORD Depositor: | Unnamed user with email elements@essex.ac.uk |
Depositing User: | Unnamed user with email elements@essex.ac.uk |
Date Deposited: | 06 Sep 2011 13:51 |
Last Modified: | 04 Dec 2024 06:19 |
URI: | http://repository.essex.ac.uk/id/eprint/60 |
Available files
Filename: 5762.full.pdf