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Fibulin‐3 is associated with tumour progression and a poor prognosis in nasopharyngeal carcinomas and inhibits cell migration and invasion via suppressed AKT activity

Nasopharyngeal carcinoma (NPC) is known for its highly metastatic character. Recent advances in diagnosis and treatment have not improved the high mortality rate that is attributable to early metastasis. Although several biomarkers correlate with metastasis and prognosis, the molecular mechanisms of...

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Published in:The Journal of pathology 2010-12, Vol.222 (4), p.367-379
Main Authors: Hwang, Chung‐Feng, Chien, Chih‐Yen, Huang, Shun‐Cheng, Yin, Yu‐Fang, Huang, Chao‐Cheng, Fang, Fu‐Min, Tsai, Hsin‐Ting, Su, Li‐Jen, Chen, Chang‐Han
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cited_by cdi_FETCH-LOGICAL-c4496-dd1d0eb0b33c9a1733493b46032256612905d57fe588f71fec6354e9772261203
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container_issue 4
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container_title The Journal of pathology
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creator Hwang, Chung‐Feng
Chien, Chih‐Yen
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Fang, Fu‐Min
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Su, Li‐Jen
Chen, Chang‐Han
description Nasopharyngeal carcinoma (NPC) is known for its highly metastatic character. Recent advances in diagnosis and treatment have not improved the high mortality rate that is attributable to early metastasis. Although several biomarkers correlate with metastasis and prognosis, the molecular mechanisms of NPC development and progression remain unclear. We demonstrate comprehensively that fibulin‐3 is down‐regulated in NPC. Loss of fibulin‐3 expression is significantly correlated with advanced tumour and lymph node‐metastasis stages, and indicates a poor 5‐year survival rate. Functionally, fibulin‐3 has the ability to suppress cell migration and invasion in NPC cancer cells by decreasing the activity of phospho‐AKT. Conversely, its depletion by fibulin‐3‐mediated siRNAs may elevate phospho‐AKT activity and significantly enhance the ability of NPC cancer cells to migrate and invade. Consistent with this negative association between fibulin‐3 and phospho‐AKT, their expression levels are inversely correlated in NPC specimens by immunohistochemical analysis. Thus, lower fibulin‐3 expression is an important indicator of poor survival. It may also contribute to the development of new therapeutic strategies to block the PI3K/AKT pathway in NPC cancer cells. Copyright © 2010 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
doi_str_mv 10.1002/path.2776
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Recent advances in diagnosis and treatment have not improved the high mortality rate that is attributable to early metastasis. Although several biomarkers correlate with metastasis and prognosis, the molecular mechanisms of NPC development and progression remain unclear. We demonstrate comprehensively that fibulin‐3 is down‐regulated in NPC. Loss of fibulin‐3 expression is significantly correlated with advanced tumour and lymph node‐metastasis stages, and indicates a poor 5‐year survival rate. Functionally, fibulin‐3 has the ability to suppress cell migration and invasion in NPC cancer cells by decreasing the activity of phospho‐AKT. Conversely, its depletion by fibulin‐3‐mediated siRNAs may elevate phospho‐AKT activity and significantly enhance the ability of NPC cancer cells to migrate and invade. Consistent with this negative association between fibulin‐3 and phospho‐AKT, their expression levels are inversely correlated in NPC specimens by immunohistochemical analysis. 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Pathol</addtitle><description>Nasopharyngeal carcinoma (NPC) is known for its highly metastatic character. Recent advances in diagnosis and treatment have not improved the high mortality rate that is attributable to early metastasis. Although several biomarkers correlate with metastasis and prognosis, the molecular mechanisms of NPC development and progression remain unclear. We demonstrate comprehensively that fibulin‐3 is down‐regulated in NPC. Loss of fibulin‐3 expression is significantly correlated with advanced tumour and lymph node‐metastasis stages, and indicates a poor 5‐year survival rate. Functionally, fibulin‐3 has the ability to suppress cell migration and invasion in NPC cancer cells by decreasing the activity of phospho‐AKT. Conversely, its depletion by fibulin‐3‐mediated siRNAs may elevate phospho‐AKT activity and significantly enhance the ability of NPC cancer cells to migrate and invade. Consistent with this negative association between fibulin‐3 and phospho‐AKT, their expression levels are inversely correlated in NPC specimens by immunohistochemical analysis. Thus, lower fibulin‐3 expression is an important indicator of poor survival. It may also contribute to the development of new therapeutic strategies to block the PI3K/AKT pathway in NPC cancer cells. Copyright © 2010 Pathological Society of Great Britain and Ireland. 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subjects 1-Phosphatidylinositol 3-kinase
AKT protein
Biological and medical sciences
biomarkers
Biomarkers, Tumor - metabolism
Cell migration
Cell Movement - physiology
Disease Progression
DNA Methylation
DNA, Neoplasm - genetics
Down-Regulation
Extracellular Matrix Proteins - metabolism
Extracellular Matrix Proteins - physiology
Female
fibulin-3
Gene Knockdown Techniques
Humans
invasion
Investigative techniques, diagnostic techniques (general aspects)
Lymph
Male
Medical sciences
Metastases
Middle Aged
migration
Molecular modelling
Mortality
Nasopharyngeal carcinoma
Nasopharyngeal Neoplasms - diagnosis
Nasopharyngeal Neoplasms - metabolism
Nasopharyngeal Neoplasms - pathology
Neoplasm Invasiveness
Neoplasm Proteins - metabolism
Neoplasm Staging
Otorhinolaryngology. Stomatology
p-AKT
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Polymerase Chain Reaction - methods
Prognosis
Promoter Regions, Genetic
Proto-Oncogene Proteins c-akt - metabolism
RNA, Small Interfering - genetics
siRNA
Survival Analysis
Tumor Cells, Cultured
Tumors
Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology
title Fibulin‐3 is associated with tumour progression and a poor prognosis in nasopharyngeal carcinomas and inhibits cell migration and invasion via suppressed AKT activity
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