HOXA1-stimulated oncogenicity is mediated by selective upregulation of components of the p44/42 MAP kinase pathway in human mammary carcinoma cells

K. M. Mohankumar, X. Q. Xu, T. Zhu, Nagarajan Kannan, L. D. Miller, E. T. Liu, P. D. Gluckman, S. Sukumar, B. S. Emerald, P. E. Lobie

Research output: Contribution to journalArticle

48 Citations (Scopus)

Abstract

Expression of homeobox A1 (HOXA1) results in oncogenic transformation of immortalized human mammary epithelial cells with aggressive tumor formation in vivo. However, the mechanisms by which HOXA1 mediates oncogenic transformation is not well defined. To identify molecules that could potentially be involved in HOXA1-mediated oncogenic transformation, microarray analysis was utilized to characterize and compare the gene expression pattern in response to forced expression or depletion of HOXA1 in human mammary carcinoma cells. Gene expression profiling identified that genes involved in the p44/42 mitogen-activated protein (MAP) kinase activation pathway (GRB2, MAP kinase kinase (MEK1) and SDFR1) or p44/42 MAP kinase-regulated genes (IER3, EPAS1, PCNA and catalase) are downstream expression targets of HOXA1. Forced expression of HOXA1 increased GRB2 and MEK1 mRNA and protein expression and increased p44/42 MAP kinase phosphorylation, activity and Elk-1-mediated transcription. Use of a MEK1 inhibitor demonstrated that increased p44/42 MAP kinase activity is required for the HOXA1-mediated increase in cell proliferation, survival, oncogenicity and oncogenic transformation. Thus, modulation of the p44/42 MAP kinase pathway is one mechanism by which HOXA1 mediates oncogenic transformation of the human mammary epithelial cell.

Original languageEnglish (US)
Pages (from-to)3998-4008
Number of pages11
JournalOncogene
Volume26
Issue number27
DOIs
StatePublished - Jun 7 2007
Externally publishedYes

Fingerprint

Homeobox Genes
Mitogen-Activated Protein Kinases
Up-Regulation
Breast Neoplasms
Breast
Epithelial Cells
Mitogen-Activated Protein Kinase Kinases
Proliferating Cell Nuclear Antigen
Gene Expression Profiling
Microarray Analysis
Catalase
Genes
Cell Survival
Phosphorylation
Cell Proliferation
Gene Expression
Messenger RNA

Keywords

  • Gene expression
  • HOXA1
  • MEK
  • Oncogenicity
  • p44/42 MAP kinase

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

Cite this

HOXA1-stimulated oncogenicity is mediated by selective upregulation of components of the p44/42 MAP kinase pathway in human mammary carcinoma cells. / Mohankumar, K. M.; Xu, X. Q.; Zhu, T.; Kannan, Nagarajan; Miller, L. D.; Liu, E. T.; Gluckman, P. D.; Sukumar, S.; Emerald, B. S.; Lobie, P. E.

In: Oncogene, Vol. 26, No. 27, 07.06.2007, p. 3998-4008.

Research output: Contribution to journalArticle

Mohankumar, KM, Xu, XQ, Zhu, T, Kannan, N, Miller, LD, Liu, ET, Gluckman, PD, Sukumar, S, Emerald, BS & Lobie, PE 2007, 'HOXA1-stimulated oncogenicity is mediated by selective upregulation of components of the p44/42 MAP kinase pathway in human mammary carcinoma cells', Oncogene, vol. 26, no. 27, pp. 3998-4008. https://doi.org/10.1038/sj.onc.1210180
Mohankumar, K. M. ; Xu, X. Q. ; Zhu, T. ; Kannan, Nagarajan ; Miller, L. D. ; Liu, E. T. ; Gluckman, P. D. ; Sukumar, S. ; Emerald, B. S. ; Lobie, P. E. / HOXA1-stimulated oncogenicity is mediated by selective upregulation of components of the p44/42 MAP kinase pathway in human mammary carcinoma cells. In: Oncogene. 2007 ; Vol. 26, No. 27. pp. 3998-4008.
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