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Published in: Medical Oncology 4/2012

01-12-2012 | Original Paper

Expression and clinical significance of NEDD9 in lung tissues

Authors: Jing-Xia Chang, Feng Gao, Guo-Qiang Zhao, Guo-Jun Zhang

Published in: Medical Oncology | Issue 4/2012

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Abstract

Neural precursor cell expressed, developmentally downregulated 9 (NEDD9) acts as a scaffold protein and belongs to a family of CAS (Crk-associated substrate) that regulates protein complexes controlling invasion and differentiation. Preclinical research for this gene was predominantly reported in melanomas, glioblastoma, and lymphoma. So we investigated the expression and significance of NEDD9 mRNA and protein in lung tissues. Specifically, we immunohistochemically compared NEDD9 expression and localization in 24 formalin-fixed and paraffin-embedded lung adenocarcinoma tissues with that of surrounding nonneoplastic tissue and five microscopically normal lungs. NEDD9 mRNA levels were quantitatively analyzed by fluorescent quantitative reverse transcription–polymerase chain reaction (FQ-PCR) in frozen tissue specimens of all tumors and 24 matched nonneoplastic lung parenchymas, and protein expression in 16 homogenates of matched neoplastic/nonneoplastic specimens was evaluated by Western blotting. The three techniques showed that NEDD9 is weakly expressed in nonneoplastic lung parenchyma and upregulated in lung adenocarcinoma. Moreover, FQ-PCR indicated a statistically significant correlation between NEDD9 upregulation and higher disease stages (I + II versus III + IV, p = 0.001; high and middle versus low differentiation, p < 0.001). Our results provide evidence that NEDD9 is upregulated in lung adenocarcinoma, and overexpression of NEDD9 protein has been strongly correlated with staging and differentiation grade and tumor size in lung adenocarcinoma, which demonstrated a poor prognosis.
Literature
1.
go back to reference Law SF, Estojak J, Wang B, et al. Human enhancer of filamentation 1 (HEF1/NEDD9/CAS-L), a novel p130Cas-Like docking protein, associates with FAK, and induces pseudohyphal growth in yeast. Mol Cell Biol. 1996;16:3327–37.PubMed Law SF, Estojak J, Wang B, et al. Human enhancer of filamentation 1 (HEF1/NEDD9/CAS-L), a novel p130Cas-Like docking protein, associates with FAK, and induces pseudohyphal growth in yeast. Mol Cell Biol. 1996;16:3327–37.PubMed
2.
go back to reference Minegishi M, Tachibana K, Sato T, et al. Structure and function of Cas-L, a 105-kD Crk-associated substrate-related protein that is involved in beta-1 integrin-mediated signaling in lymphocytes. J Exp Med. 1996;184:1365–75.PubMedCrossRef Minegishi M, Tachibana K, Sato T, et al. Structure and function of Cas-L, a 105-kD Crk-associated substrate-related protein that is involved in beta-1 integrin-mediated signaling in lymphocytes. J Exp Med. 1996;184:1365–75.PubMedCrossRef
3.
go back to reference Kumar S, Tomooka Y, Noda M. Identification of a set of genes with developmentally down-regulated expression in the mouse brain. Biochem Biophys Res Commun. 1992;185:1155–61.PubMedCrossRef Kumar S, Tomooka Y, Noda M. Identification of a set of genes with developmentally down-regulated expression in the mouse brain. Biochem Biophys Res Commun. 1992;185:1155–61.PubMedCrossRef
4.
go back to reference Tikhmyanova N, Little JL, Golemis EA. CAS proteins in normal and pathological cell growth control. Cellular Mol Life Sci. 2010;67(7):1025–48.CrossRef Tikhmyanova N, Little JL, Golemis EA. CAS proteins in normal and pathological cell growth control. Cellular Mol Life Sci. 2010;67(7):1025–48.CrossRef
5.
go back to reference Minn AJ, Gupta GP, Siegel PM, et al. Genes that mediate breast cancer metastasis to lung. Nature. 2005;436:518–24.PubMedCrossRef Minn AJ, Gupta GP, Siegel PM, et al. Genes that mediate breast cancer metastasis to lung. Nature. 2005;436:518–24.PubMedCrossRef
6.
go back to reference Natarajan M, Stewart JE, Golemis EA, et al. HEF1 is a necessary and specific downstream effector of FAK that promotes the migration of glioblastoma cells. Oncogene. 2006;25:1721–32.PubMedCrossRef Natarajan M, Stewart JE, Golemis EA, et al. HEF1 is a necessary and specific downstream effector of FAK that promotes the migration of glioblastoma cells. Oncogene. 2006;25:1721–32.PubMedCrossRef
7.
go back to reference Kim M, Gans JD, Nogueira C, et al. Comparative oncogenomics identifies NEDD9 as a melanoma metastasis gene. Cell. 2006;125:1269–81.PubMedCrossRef Kim M, Gans JD, Nogueira C, et al. Comparative oncogenomics identifies NEDD9 as a melanoma metastasis gene. Cell. 2006;125:1269–81.PubMedCrossRef
8.
9.
go back to reference Tuveson DA, Jacks T. Modeling human lung cancer in mice: similarities and shortcomings. Oncogene. 1999;18:5318–24.PubMedCrossRef Tuveson DA, Jacks T. Modeling human lung cancer in mice: similarities and shortcomings. Oncogene. 1999;18:5318–24.PubMedCrossRef
10.
go back to reference Carelli S, Zadra G, Vaira V, et al. Up-regulation of focal adhesion kinase in non-small cell lung cancer. Lung Cancer (Amsterdam, Netherlands). 2006;53:263–71.CrossRef Carelli S, Zadra G, Vaira V, et al. Up-regulation of focal adhesion kinase in non-small cell lung cancer. Lung Cancer (Amsterdam, Netherlands). 2006;53:263–71.CrossRef
11.
go back to reference Liu N, Bi F, Pan Y, et al. Reversal of the malignant phenotype of gastric cancer cells by inhibition of RhoA expression and activity. Clin Cancer Res. 2004;10(18 Pt 1):6239–47.PubMedCrossRef Liu N, Bi F, Pan Y, et al. Reversal of the malignant phenotype of gastric cancer cells by inhibition of RhoA expression and activity. Clin Cancer Res. 2004;10(18 Pt 1):6239–47.PubMedCrossRef
12.
go back to reference Falleni M, Pellegrini C, Marchetti A, et al. Survivin gene expression in early-stage nonsmall cell lung cancer. J Pathol. 2003;200:620–6.PubMedCrossRef Falleni M, Pellegrini C, Marchetti A, et al. Survivin gene expression in early-stage nonsmall cell lung cancer. J Pathol. 2003;200:620–6.PubMedCrossRef
13.
go back to reference Astier A, Manie SN, Law SF, et al. Association of the Cas-like molecule HEF1 with CrkL following integrin and antigen receptor signaling in human B-cells: potential relevance to neoplastic lymphohematopoietic cells. Leuk Lymphoma. 1997;28:65–72.PubMed Astier A, Manie SN, Law SF, et al. Association of the Cas-like molecule HEF1 with CrkL following integrin and antigen receptor signaling in human B-cells: potential relevance to neoplastic lymphohematopoietic cells. Leuk Lymphoma. 1997;28:65–72.PubMed
14.
go back to reference le Thao B, Vu HA, Yasuda K, et al. Cas-L was overexpressed in imatinib-resistant gastrointestinal stromal tumor cells. Cancer Biol Ther. 2009;8:683–8.CrossRef le Thao B, Vu HA, Yasuda K, et al. Cas-L was overexpressed in imatinib-resistant gastrointestinal stromal tumor cells. Cancer Biol Ther. 2009;8:683–8.CrossRef
15.
go back to reference Iwata S, Souta-Kuribara A, Yamakawa A, et al. HTLV-I Tax induces and associates with Crk-associated substrate lymphocyte type (Cas-L). Oncogene. 2005;24:1262–71.PubMedCrossRef Iwata S, Souta-Kuribara A, Yamakawa A, et al. HTLV-I Tax induces and associates with Crk-associated substrate lymphocyte type (Cas-L). Oncogene. 2005;24:1262–71.PubMedCrossRef
16.
go back to reference Ji H, Ramsey MR, Hayes DN, et al. LKB1 modulates lung cancer differentiation and metastasis. Nature. 2007;448:807–10.PubMedCrossRef Ji H, Ramsey MR, Hayes DN, et al. LKB1 modulates lung cancer differentiation and metastasis. Nature. 2007;448:807–10.PubMedCrossRef
17.
go back to reference Fashena SJ, Einarson MB, O’Neill GM, et al. Dissection of HEF1-dependent functions in motility and transcriptional regulation. J Cell Sci. 2002;115:99–111.PubMed Fashena SJ, Einarson MB, O’Neill GM, et al. Dissection of HEF1-dependent functions in motility and transcriptional regulation. J Cell Sci. 2002;115:99–111.PubMed
18.
go back to reference Law SF, O’Neill GM, Fashena SJ, et al. The docking protein HEF1/NEDD9/CAS-L is an apoptotic mediator at focal adhesion sites. Mol Cell Biol. 2000;20:5184–95.PubMedCrossRef Law SF, O’Neill GM, Fashena SJ, et al. The docking protein HEF1/NEDD9/CAS-L is an apoptotic mediator at focal adhesion sites. Mol Cell Biol. 2000;20:5184–95.PubMedCrossRef
19.
go back to reference Pugacheva EN, Golemis EA. The focal adhesion scaffolding protein HEF1/NEDD9/CAS-L regulates activation of the Aurora-A and Nek2 kinases at the centrosome. Nat Cell Biol. 2005;7:937–46.PubMedCrossRef Pugacheva EN, Golemis EA. The focal adhesion scaffolding protein HEF1/NEDD9/CAS-L regulates activation of the Aurora-A and Nek2 kinases at the centrosome. Nat Cell Biol. 2005;7:937–46.PubMedCrossRef
20.
go back to reference Nakamoto T, Sakai R, Honda H, et al. Requirements for localization of p130cas to focal adhesions. Mol Cell Biol. 1997;17:3884–97.PubMed Nakamoto T, Sakai R, Honda H, et al. Requirements for localization of p130cas to focal adhesions. Mol Cell Biol. 1997;17:3884–97.PubMed
21.
go back to reference van Seventer GA, Salmen HJ, Law SF, et al. Focal adhesion kinase regulates beta1 integrin-dependent T cell migration through an HEF1 effector pathway. Eur J Immunol. 2001;31:1417–27.PubMedCrossRef van Seventer GA, Salmen HJ, Law SF, et al. Focal adhesion kinase regulates beta1 integrin-dependent T cell migration through an HEF1 effector pathway. Eur J Immunol. 2001;31:1417–27.PubMedCrossRef
Metadata
Title
Expression and clinical significance of NEDD9 in lung tissues
Authors
Jing-Xia Chang
Feng Gao
Guo-Qiang Zhao
Guo-Jun Zhang
Publication date
01-12-2012
Publisher
Springer US
Published in
Medical Oncology / Issue 4/2012
Print ISSN: 1357-0560
Electronic ISSN: 1559-131X
DOI
https://doi.org/10.1007/s12032-012-0213-0

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