Literature DB >> 22935821

Expression of HOXD3 correlates with shorter survival in patients with invasive breast cancer.

Cheng Shaoqiang1, Zhang Yue, Liu Yang, Zhao Hong, Zhen Lina, Pang Da, Zhang Qingyuan.   

Abstract

Hox genes encode a family of homeodomain-containing transcription factors that determine cellular identity during development and which are also expressed in some types of cancer. The HOXD3 gene, a member of the Hox gene family, has been demonstrated to be expressed in several tumor cell lines, which exhibit enhanced invasion and metastasis through coordinate expression of metastasis-associated factors. However, the clinical impact of HOXD3 in breast cancer remains unclear. In the current study, we examined the expression of HOXD3 and integrin β3 by immunohistochemical staining in patients with invasive breast cancer. We found that HOXD3 expression was significantly frequent in high histopathological grade and hormone-receptor negative breast cancer patients. The expression of HOXD3 was closely associated with integrin β3 expression. Furthermore, patients with high HOXD3 expression levels in their breast tumors had significantly shorter survival times than patients in which HOXD3 was weakly expressed in breast tumors. Univariate and multivariate analyses confirmed that increased HOXD3-expression was an independent and significant factor in predicting poor prognosis for patients with breast cancer. In conclusion, HOXD3 expression is a significant unfavorable prognostic factor for patients with invasive breast cancer and as such is a potentially useful prognostic marker for breast cancer.

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Year:  2012        PMID: 22935821     DOI: 10.1007/s10585-012-9524-y

Source DB:  PubMed          Journal:  Clin Exp Metastasis        ISSN: 0262-0898            Impact factor:   5.150


  33 in total

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8.  Whole exome sequencing of an asbestos-induced wild-type murine model of malignant mesothelioma.

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9.  Identification of IDH-mutant gliomas by a prognostic signature according to gene expression profiling.

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