RRC ID 21156
Author Oda T, Tian T, Inoue M, Ikeda J, Qiu Y, Okumura M, Aozasa K, Morii E.
Title Tumorigenic role of orphan nuclear receptor NR0B1 in lung adenocarcinoma.
Journal Am J Pathol
Abstract Cancer stem cells are a limited population of tumor cells that are thought to reconstitute whole tumors. The Hoechst dye exclusion assay revealed that tumors are composed of both a main population and a side population of cells, which are rich in cancer stem cells. NR0B1 is an orphan nuclear receptor that is expressed to a greater extent in the side population, as compared with the main population, of a lung adenocarcinoma cell line. In this study, we investigated the role of NR0B1 in lung adenocarcinoma cells. Reduction of NR0B1 expression levels in lung adenocarcinoma cell lines resulted in vulnerability to anti-cancer drugs and decreased abilities for invasion, in vitro colony formation, and tumorigenicity in non-obese diabetic/severe compromised immunodeficient mice. When 193 cases of lung adenocarcinoma were immunohistochemically examined, higher levels of NR0B1 expression correlated with higher rates of lymph node metastasis and recurrence. Multivariate analysis revealed high NR0B1 expression levels, stage of the disease, and size of tumor to be independent unfavorable prognostic factors for overall and disease-free survival rates. In clinical samples, NR0B1 expression levels inversely correlated to the proportion of methylated CpG sequences around the transcription initiation site of the NR0B1 gene, suggesting the epigenetic control of NR0B1 transcription in lung adenocarcinoma. In conclusion, NR0B1 might play a role in the malignant potential of lung adenocarcinoma.
Volume 175(3)
Pages 1235-45
Published 2009-9-1
DOI 10.2353/ajpath.2009.090010
PII S0002-9440(10)60633-5
PMID 19644015
PMC PMC2731142
MeSH Adenocarcinoma / metabolism* Adenocarcinoma / mortality Adenocarcinoma / pathology Animals Biomarkers, Tumor* Cell Line, Tumor DAX-1 Orphan Nuclear Receptor / biosynthesis* DAX-1 Orphan Nuclear Receptor / genetics Disease-Free Survival Female Gene Expression Regulation, Neoplastic Humans Lung Neoplasms / metabolism* Lung Neoplasms / mortality Lung Neoplasms / pathology Lymphatic Metastasis / genetics Methylation Mice Mice, Inbred NOD Mice, SCID Neoplasm Invasiveness / genetics Neoplasm Transplantation Prognosis Promoter Regions, Genetic Recurrence Transcription, Genetic
Times Cited 12
WOS Category CELL BIOLOGY
Resource
Human and Animal Cells PC-14(RCB0446)