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Erschienen in: Clinical & Experimental Metastasis 2/2013

01.02.2013 | Research Paper

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

verfasst von: Cheng Shaoqiang, Zhang Yue, Liu Yang, Zhao Hong, Zhen Lina, Pang Da, Zhang Qingyuan

Erschienen in: Clinical & Experimental Metastasis | Ausgabe 2/2013

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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.
Literatur
1.
3.
Zurück zum Zitat Graham A, Papalopulu N, Krumlauf R (1989) The murine and Drosophila homeobox gene complexes have common features of organization and expression. Cell 57:367–378PubMedCrossRef Graham A, Papalopulu N, Krumlauf R (1989) The murine and Drosophila homeobox gene complexes have common features of organization and expression. Cell 57:367–378PubMedCrossRef
4.
5.
Zurück zum Zitat Levine M, Hoey T (1988) Homeobox proteins as sequence-specific transcription factors. Cell 55:537–540PubMedCrossRef Levine M, Hoey T (1988) Homeobox proteins as sequence-specific transcription factors. Cell 55:537–540PubMedCrossRef
7.
Zurück zum Zitat Mark M, Rijli FM, Chambon P (1997) Homeobox genes in embryogenesis and pathogenesis. Pediatr Res 42:421–429PubMedCrossRef Mark M, Rijli FM, Chambon P (1997) Homeobox genes in embryogenesis and pathogenesis. Pediatr Res 42:421–429PubMedCrossRef
8.
Zurück zum Zitat Takahashi Y et al (2004) Expression profiles of 39 HOX genes in normal human adult organs and anaplastic thyroid cancer cell lines by quantitative real-time RT-PCR system. Exp Cell Res 293:144–153PubMedCrossRef Takahashi Y et al (2004) Expression profiles of 39 HOX genes in normal human adult organs and anaplastic thyroid cancer cell lines by quantitative real-time RT-PCR system. Exp Cell Res 293:144–153PubMedCrossRef
9.
Zurück zum Zitat Abate-Shen C (2002) Deregulated homeobox gene expression in cancer: cause or consequence? Nat Rev Cancer 2:777–785PubMedCrossRef Abate-Shen C (2002) Deregulated homeobox gene expression in cancer: cause or consequence? Nat Rev Cancer 2:777–785PubMedCrossRef
10.
Zurück zum Zitat Raman V et al (2000) Compromised HOXA5 function can limit p53 expression in human breast tumours. Nature 405:974–978PubMedCrossRef Raman V et al (2000) Compromised HOXA5 function can limit p53 expression in human breast tumours. Nature 405:974–978PubMedCrossRef
11.
Zurück zum Zitat Trivedi CM, Patel RC, Patel CV (2007) Homeobox gene HOXA9 inhibits nuclear factor-kappa B dependent activation of endothelium. Atherosclerosis 195:e50–e60PubMedCrossRef Trivedi CM, Patel RC, Patel CV (2007) Homeobox gene HOXA9 inhibits nuclear factor-kappa B dependent activation of endothelium. Atherosclerosis 195:e50–e60PubMedCrossRef
12.
Zurück zum Zitat Trivedi CM, Patel RC, Patel CV (2008) Differential regulation of HOXA9 expression by nuclear factor kappa B (NF-kappaB) and HOXA9. Gene 408:187–195PubMedCrossRef Trivedi CM, Patel RC, Patel CV (2008) Differential regulation of HOXA9 expression by nuclear factor kappa B (NF-kappaB) and HOXA9. Gene 408:187–195PubMedCrossRef
13.
Zurück zum Zitat Wu X et al (2006) HOXB7, a homeodomain protein, is overexpressed in breast cancer and confers epithelial–mesenchymal transition. Cancer Res 66:9527–9534PubMedCrossRef Wu X et al (2006) HOXB7, a homeodomain protein, is overexpressed in breast cancer and confers epithelial–mesenchymal transition. Cancer Res 66:9527–9534PubMedCrossRef
14.
Zurück zum Zitat Condie BG, Capecchi MR (1993) Mice homozygous for a targeted disruption of Hoxd-3 (Hox-4.1) exhibit anterior transformations of the first and second cervical vertebrae, the atlas and the axis. Development 119:579–595PubMed Condie BG, Capecchi MR (1993) Mice homozygous for a targeted disruption of Hoxd-3 (Hox-4.1) exhibit anterior transformations of the first and second cervical vertebrae, the atlas and the axis. Development 119:579–595PubMed
15.
Zurück zum Zitat Manley NR, Capecchi MR (1998) Hox group 3 paralogs regulate the development and migration of the thymus, thyroid, and parathyroid glands. Dev Biol 195:1–15PubMedCrossRef Manley NR, Capecchi MR (1998) Hox group 3 paralogs regulate the development and migration of the thymus, thyroid, and parathyroid glands. Dev Biol 195:1–15PubMedCrossRef
16.
Zurück zum Zitat Hamada J et al (2001) Overexpression of homeobox gene HOXD3 induces coordinate expression of metastasis-related genes in human lung cancer cells. Int J Cancer 93:516–525CrossRef Hamada J et al (2001) Overexpression of homeobox gene HOXD3 induces coordinate expression of metastasis-related genes in human lung cancer cells. Int J Cancer 93:516–525CrossRef
17.
Zurück zum Zitat Taniguchi Y, Komatsu N, Moriuchi T (1995) Overexpression of the HOX4A (HOXD3) homeobox gene in human erythroleukemia HEL cells results in altered adhesive properties. Blood 85:2786–2794PubMed Taniguchi Y, Komatsu N, Moriuchi T (1995) Overexpression of the HOX4A (HOXD3) homeobox gene in human erythroleukemia HEL cells results in altered adhesive properties. Blood 85:2786–2794PubMed
18.
Zurück zum Zitat Haybittle JL et al (1982) A prognostic index in primary breast cancer. Br J Cancer 45:361–366PubMedCrossRef Haybittle JL et al (1982) A prognostic index in primary breast cancer. Br J Cancer 45:361–366PubMedCrossRef
19.
Zurück zum Zitat Kowalski PJ, Rubin MA, Kleer CG (2003) E-cadherin expression in primary carcinomas of the breast and its distant metastases. Breast Cancer Res 5:R217–R222PubMedCrossRef Kowalski PJ, Rubin MA, Kleer CG (2003) E-cadherin expression in primary carcinomas of the breast and its distant metastases. Breast Cancer Res 5:R217–R222PubMedCrossRef
20.
Zurück zum Zitat Huber GF et al (2011) Down regulation of E-cadherin (ECAD)—a predictor for occult metastatic disease in sentinel node biopsy of early squamous cell carcinomas of the oral cavity and oropharynx. BMC cancer 11(217):1–8PubMed Huber GF et al (2011) Down regulation of E-cadherin (ECAD)—a predictor for occult metastatic disease in sentinel node biopsy of early squamous cell carcinomas of the oral cavity and oropharynx. BMC cancer 11(217):1–8PubMed
21.
Zurück zum Zitat Kashiwagi S et al (2010) Significance of E-cadherin expression in triple-negative breast cancer. Br J Cancer 103:249–255PubMedCrossRef Kashiwagi S et al (2010) Significance of E-cadherin expression in triple-negative breast cancer. Br J Cancer 103:249–255PubMedCrossRef
22.
Zurück zum Zitat Frixen UH et al (1991) E-cadherin-mediated cell–cell adhesion prevents invasiveness of human carcinoma cells. J Cell Biol 113:173–185PubMedCrossRef Frixen UH et al (1991) E-cadherin-mediated cell–cell adhesion prevents invasiveness of human carcinoma cells. J Cell Biol 113:173–185PubMedCrossRef
23.
Zurück zum Zitat Vleminckx K et al (1991) Genetic manipulation of E-cadherin expression by epithelial tumor cells reveals an invasion suppressor role. Cell 66:107–119PubMedCrossRef Vleminckx K et al (1991) Genetic manipulation of E-cadherin expression by epithelial tumor cells reveals an invasion suppressor role. Cell 66:107–119PubMedCrossRef
24.
Zurück zum Zitat Watabe M et al (1994) Induction of polarized cell–cell association and retardation of growth by activation of the E-cadherin-catenin adhesion system in a dispersed carcinoma line. J Cell Biol 127:247–256PubMedCrossRef Watabe M et al (1994) Induction of polarized cell–cell association and retardation of growth by activation of the E-cadherin-catenin adhesion system in a dispersed carcinoma line. J Cell Biol 127:247–256PubMedCrossRef
25.
Zurück zum Zitat Mariotti A et al (2007) N-cadherin as a therapeutic target in cancer. Expert Opin Investig Drugs 16:451–465PubMedCrossRef Mariotti A et al (2007) N-cadherin as a therapeutic target in cancer. Expert Opin Investig Drugs 16:451–465PubMedCrossRef
26.
Zurück zum Zitat Cavallaro U (2004) N-cadherin as an invasion promoter: a novel target for antitumor therapy? Curr Opin Investig Drugs 5:1274–1278PubMed Cavallaro U (2004) N-cadherin as an invasion promoter: a novel target for antitumor therapy? Curr Opin Investig Drugs 5:1274–1278PubMed
27.
Zurück zum Zitat Hazan RB et al (2000) Exogenous expression of N-cadherin in breast cancer cells induces cell migration, invasion, and metastasis. J Cell Biol 148:779–790PubMedCrossRef Hazan RB et al (2000) Exogenous expression of N-cadherin in breast cancer cells induces cell migration, invasion, and metastasis. J Cell Biol 148:779–790PubMedCrossRef
28.
Zurück zum Zitat Planaguma J et al (2011) Matrix metalloproteinase-2 and matrix metalloproteinase-9 codistribute with transcription factors RUNX1/AML1 and ETV5/ERM at the invasive front of endometrial and ovarian carcinoma. Hum Pathol 42:57–67PubMedCrossRef Planaguma J et al (2011) Matrix metalloproteinase-2 and matrix metalloproteinase-9 codistribute with transcription factors RUNX1/AML1 and ETV5/ERM at the invasive front of endometrial and ovarian carcinoma. Hum Pathol 42:57–67PubMedCrossRef
29.
Zurück zum Zitat Shen Q et al (2010) Tissue inhibitor of metalloproteinase-2 regulates matrix metalloproteinase-2-mediated endothelial barrier dysfunction and breast cancer cell transmigration through lung microvascular endothelial cells. Mol Cancer Res 8:939–951PubMed Shen Q et al (2010) Tissue inhibitor of metalloproteinase-2 regulates matrix metalloproteinase-2-mediated endothelial barrier dysfunction and breast cancer cell transmigration through lung microvascular endothelial cells. Mol Cancer Res 8:939–951PubMed
30.
Zurück zum Zitat Takayama S et al (2005) The relationship between bone metastasis from human breast cancer and integrin alpha(v)beta3 expression. Anticancer Res 25:79–83PubMed Takayama S et al (2005) The relationship between bone metastasis from human breast cancer and integrin alpha(v)beta3 expression. Anticancer Res 25:79–83PubMed
31.
Zurück zum Zitat Scatena M et al (1998) NF-kappaB mediates alphavbeta3 integrin-induced endothelial cell survival. J Cell Biol 141:1083–1093PubMedCrossRef Scatena M et al (1998) NF-kappaB mediates alphavbeta3 integrin-induced endothelial cell survival. J Cell Biol 141:1083–1093PubMedCrossRef
32.
Zurück zum Zitat Matter ML, Ruoslahti E (2001) A signaling pathway from the alpha5beta1 and alpha(v)beta3 integrins that elevates bcl-2 transcription. J Biol Chem 276:27757–27763PubMedCrossRef Matter ML, Ruoslahti E (2001) A signaling pathway from the alpha5beta1 and alpha(v)beta3 integrins that elevates bcl-2 transcription. J Biol Chem 276:27757–27763PubMedCrossRef
33.
Zurück zum Zitat De S et al (2005) VEGF-integrin interplay controls tumor growth and vascularization. Proc Natl Acad Sci USA 102:7589–7594PubMedCrossRef De S et al (2005) VEGF-integrin interplay controls tumor growth and vascularization. Proc Natl Acad Sci USA 102:7589–7594PubMedCrossRef
Metadaten
Titel
Expression of HOXD3 correlates with shorter survival in patients with invasive breast cancer
verfasst von
Cheng Shaoqiang
Zhang Yue
Liu Yang
Zhao Hong
Zhen Lina
Pang Da
Zhang Qingyuan
Publikationsdatum
01.02.2013
Verlag
Springer Netherlands
Erschienen in
Clinical & Experimental Metastasis / Ausgabe 2/2013
Print ISSN: 0262-0898
Elektronische ISSN: 1573-7276
DOI
https://doi.org/10.1007/s10585-012-9524-y

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