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CENP-F expression is associated with poor prognosis and chromosomal instability in patients with primary breast cancer

O'Brien, Sallyarm L. (author)
Fagan, Ailis (author)
Fox, Edward J. P. (author)
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Millikan, Robert C. (author)
Culhane, Aedin C. (author)
Brennan, Donal J. (author)
McCann, Amanda H. (author)
Hegarty, Shauna (author)
Moyna, Siobhan (author)
Duffy, Michael J. (author)
HigginS, Desmond G. (author)
Jirström, Karin (author)
Lund University,Lunds universitet,Tumörmikromiljö,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Tumor microenvironment,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine
Landberg, Göran (author)
Lund University,Lunds universitet,Patologi, Malmö,Forskargrupper vid Lunds universitet,Pathology, Malmö,Lund University Research Groups
Gallagher, William M. (author)
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 (creator_code:org_t)
2007-01-04
2007
English.
In: International Journal of Cancer. - : Wiley. - 0020-7136. ; 120:7, s. 1434-1443
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • DNA microarrays have the potential to classify tumors according to their transcriptome. Tissue microarrays (TMAs) facilitate the validation of biomarkers by offering a high-throughput approach to sample analysis. We reanalyzed a high profile breast cancer DNA microarray dataset containing 96 tumor samples using a powerful statistical approach, between group analyses. Among the genes we identified was centromere protein-F (CENP-F), a gene associated with poor prognosis. In a published follow-up breast cancer DNA microarray study, comprising 295 tumour samples, we found that CENP-F upregulation was significantly associated with worse overall survival (p < 0.001) and reduced metastasis-free survival (p < 0.001). To validate and expand upon these findings, we used 2 independent breast cancer patient cohorts represented on TMAs. CENP-F protein expression was evaluated by immunohistochemistry in 91 primary breast cancer samples from cohort I and 289 samples from cohort II. CENP-F correlated with markers of aggressive tumor behavior including ER negativity and high tumor grade. In cohort I, CENP-F was significantly associated with markers of CIN including cyclin E, increased telomerase activity, c-Myc amplification and aneuploidy. In cohort II CENP-F correlated with VEGFR2, phosphorylated Ets-2 and Ki67, and in multivariate analysis, was an independent predictor of worse breast cancer-specific survival (p = 0.036) and overall survival (p = 0.040). In conclusion, we identified CENP-F as a biomarker associated with poor outcome in breast cancer and showed several novel associations of biological significance. (c) 2007 Wiley-Liss, Inc.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

CENP-F
prognosis
tissue microarrays
breast cancer
DNA microarrays
chromosomal instability

Publication and Content Type

art (subject category)
ref (subject category)

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