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PMID: 14977834 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Down regulation of high in normal-1 (HIN-1) is a frequent event in stage I non-small cell lung cancer and correlates with poor clinical outcome.

Marchetti A, Barassi F, Martella C, Chella A, Salvatore S, Castrataro A, Mucilli F, Sacco R, Buttitta F

Abstract

The aim of this study was to evaluate the prevalence and the clinical significance of HIN-1 mRNA expression in early stage non-small cell lung carcinomas (NSCLCs). A series of 91 NSCLC patients with stage I neoplastic disease was studied. HIN-1 expression was investigated by quantitative real-time reverse transcription-PCR on tumor specimens and matching normal lung tissues. Variables were analyzed by chi(2) test and Fisher's exact tests. Survival was evaluated with the method of Kaplan-Meier. Multivariate analysis was performed with Cox's proportional hazards model. Seventy one (78%) tumors showed a reduction of HIN-1 mRNA compared with the normal counterpart. The range of reduction varied greatly, from -2-fold to -3350-fold. Setting a cutoff at -46-fold (median value of HIN-1 mRNA reduction), 46 cases (51%) had a markedly reduced expression, and 45 cases (49%) showed a normal or slightly reduced expression. A statistically significant association between low HIN-1 mRNA levels and T status was observed (P = 0.036). Univariate survival curves, estimated using the method of Kaplan-Meier, defined a significant association between HIN-1 expression and both overall survival (P = 0.0095) and disease-free survival (P = 0.0122). A multivariate analysis, performed by Cox's proportional hazards regression model, confirmed that a low HIN-1 expression was the only significant factor to predict poor prognosis. Our data indicate that HIN-1 expression, measured by real-time reverse transcription-PCR, is a possible prognostic factor in patients with stage I NSCLC. Additional studies are required to further validate this potential prognostic marker.

MeSH Terms
Adult Aged Biomarkers, Tumor Carcinoma, Non-Small-Cell Lung/metabolism Cytokines/biosynthesis DNA Primers/pharmacology DNA, Complementary/metabolism Disease-Free Survival Down-Regulation Female Humans Lung/pathology Lung Neoplasms/metabolism Male Middle Aged Multivariate Analysis Polymerase Chain Reaction Prognosis RNA, Messenger/metabolism Reverse Transcriptase Polymerase Chain Reaction Time Factors Treatment Outcome Tumor Suppressor Proteins/biosynthesis
Chemicals
Biomarkers, Tumor Cytokines DNA Primers DNA, Complementary RNA, Messenger SCGB3A1 protein, human Tumor Suppressor Proteins
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Marchetti Antonio
Department of Oncology, University G. D'Annunzio, Chieti, Italy. amarchetti@unich.it
Barassi Fabio
Martella Carla
Chella Antonio
Salvatore Simona
Castrataro Antonio
Mucilli Felice
Sacco Rocco
Buttitta Fiamma
Article Info
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Abbr.
Clin Cancer Res
ISSN
1078-0432
Published
2004-02-15
Pages
1338-43
Language
English
Region
United States
NLM ID
9502500
Subset
IM
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