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Neoplasma Vol.53, p.530-537, 2006 |
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Title: Transfection of nm23-H1 increased expression of -Catenin, E-Cadherin and TIMP-1 and decreased the expression of MMP-2, CD44v6 and VEGF and inhibited the metastatic potential of human non-small cell lung cancer cell line L9981 | ||
Author: G. CHE, J. CHEN, L. LIU, Y. WANG, L. LI, Y. QIN, Q. ZHOU | ||
Abstract: Nm23 is a metastasis suppressor gene. In this report, we transfected nm23-H1 cDNA into L9981, a human large cell lung
cancer cell line with nm23 negative expression, and made a stable transfectant. L9981-nm23-H1 cells exhibited lower cells proliferation rate, more G0/G1 phase growth and an increase in apoptosis with a dramatic decreased in the tumor cells ability
to metastasize. L9981-nm23-H1 cells also demonstrated a significantly reduced lymph node and pulmonary metastatic capacity in vivo when injected into the nude mice. Furthermore, we used DNAmicroarray analysis to explore the change in expression of the metastasis-related genes in L9981-nm23-H1 cells. We found that the expression of β-Catenin, E-Cadherin
and TIMP-1 were significantly increased while expression MMP-2, CD44v6, and VEGF was dramatically decreased in
L9981-nm23-H1, as confirmed by RT-PCR and western blot. These results demonstrated that nm23-H1 can suppress the mobility and metastatic capacity of cancer cells and the molecular mechanism by which nm23-H1 suppresses tumor metastasis may be via increasing the expression of metastasis-related genes such as β-Catenin, E-Cadherin and TIMP-1 and decreasing the expression of MMP-2, CD44V6 and VEGF. |
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Keywords: nm23-H1, metastasis suppressor gene, lung cancer, L9981 cell line | ||
Year: 2006, Volume: 53, Issue: | Page From: 530, Page To: 537 | |
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