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PMID: 12566310 Published · ppublish English Journal Article

Computational analysis and experimental validation of tumor-associated alternative RNA splicing in human cancer.

Cancer research ·Vol. 63 ·No. 3 ·2003-02-01 ·Pages 655-7

Wang Z, Lo HS, Yang H, Gere S, Hu Y, Buetow KH, Lee MP

Abstract

A genome-wide computational screen was performed to identify tumor-associated alternative RNA splicing isoforms. A BLAST algorithm was used to compare 11,014 genes from RefSeq with 3,471,822 human expressed sequence tag sequences. The screen identified 26,258 alternative splicing isoforms of which 845 were significantly associated with human cancer, and 54 were specifically associated with liver cancer. Furthermore, canonical GT-AG splice junctions were used significantly less frequently in the alternative splicing isoforms in tumors. Reverse transcription-PCR experiments confirmed association of the alternative splicing isoforms with tumors. These results suggest that alternative splicing may have potential as a diagnostic marker for cancer.

MeSH Terms
Algorithms Alternative Splicing Computational Biology/methods Databases, Nucleic Acid Expressed Sequence Tags Genetic Markers/genetics Genome, Human Humans Liver Neoplasms/genetics Neoplasms/genetics,metabolism Reproducibility of Results Reverse Transcriptase Polymerase Chain Reaction
Chemicals
Genetic Markers
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Wang Zhining
Laboratory of Population Genetics, National Cancer Institute, National Institutes of Health, Gaithersburg, Maryland 20877,USA.
Lo H Shuen
Yang Howard
Gere Sheryl
Hu Ying
Buetow Kenneth H
Lee Maxwell P
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
2003-02-01
Pages
655-7
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Corrections
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