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PLoS One. 2014 Aug 20;9(8):e105639. doi: 10.1371/journal.pone.0105639. eCollection 2014.

Gene expression profiling in human lung development: an abundant resource for lung adenocarcinoma prognosis.

Author information

1
State Key Laboratory of Molecular Oncology, Department of Etiology and Carcinogenesis, Cancer Hospital and Institute, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.
2
Department of Gynaecology and Obstetrics, Maternal & Child Health Care hospital of Haidian, Beijing, China.
3
Departments of Thoracic Surgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
4
Department of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
5
College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
6
Departments of Thoracic Surgery, Cancer Hospital and Institute, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.
7
Medical Genome Facility, and the Department of Laboratory Medicine and Pathology, Mayo Clinic. Rochester, Minnesota, United States of America.

Abstract

A tumor can be viewed as a special "organ" that undergoes aberrant and poorly regulated organogenesis. Progress in cancer prognosis and therapy might be facilitated by re-examining distinctive processes that operate during normal development, to elucidate the intrinsic features of cancer that are significantly obscured by its heterogeneity. The global gene expression signatures of 44 human lung tissues at four development stages from Asian descent and 69 lung adenocarcinoma (ADC) tissue samples from ethnic Chinese patients were profiled using microarrays. All of the genes were classified into 27 distinct groups based on their expression patterns (named as PTN1 to PTN27) during the developmental process. In lung ADC, genes whose expression levels decreased steadily during lung development (genes in PTN1) generally had their expression reactivated, while those with uniformly increasing expression levels (genes in PTN27) had their expression suppressed. The genes in PTN1 contain many n-gene signatures that are of prognostic value for lung ADC. The prognostic relevance of a 12-gene demonstrator for patient survival was characterized in five cohorts of healthy and ADC patients [ADC_CICAMS (n = 69, p = 0.007), ADC_PNAS (n = 125, p = 0.0063), ADC_GSE13213 (n = 117, p = 0.0027), ADC_GSE8894 (n =  2, p = 0.01), and ADC_NCI (n = 282, p = 0.045)] and in four groups of stage I patients [ADC_CICAMS (n = 22, p = 0.017), ADC_PNAS (n = 76, p = 0.018), ADC_GSE13213 (n = 79, p = 0.02), and ADC_qPCR (n = 62, p = 0.006)]. In conclusion, by comparison of gene expression profiles during human lung developmental process and lung ADC progression, we revealed that the genes with a uniformly decreasing expression pattern during lung development are of enormous prognostic value for lung ADC.

PMID:
25141350
PMCID:
PMC4139381
DOI:
10.1371/journal.pone.0105639
[Indexed for MEDLINE]
Free PMC Article

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