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Cancer Res. 2012 May 15;72(10):2512-21. doi: 10.1158/0008-5472.CAN-11-3870. Epub 2012 Mar 20.

AMPKα modulation in cancer progression: multilayer integrative analysis of the whole transcriptome in Asian gastric cancer.

Author information

1
Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030,USA.
2
Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
3
Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
4
Department of Internal Medicine, Yonsei University College of Medicine, Seoul 120-749, Korea.
5
Department of Surgery, Yonsei University College of Medicine, Seoul 120-749, Korea.
6
Department of Pathology, Yonsei University College of Medicine, Seoul 120-749, Korea.
7
Partek Inc., St. Louis, MO 63141, USA.
8
Life Technologies, Foster City, CA 94404, USA.
#
Contributed equally

Abstract

Gastric cancer is the most common cancer in Asia and most developing countries. Despite the use of multimodality therapeutics, it remains the second leading cause of cancer death in the world. To identify the molecular underpinnings of gastric cancer in the Asian population, we applied an RNA-sequencing approach to gastric tumor and noncancerous specimens, generating 680 million informative short reads to quantitatively characterize the entire transcriptome of gastric cancer (including mRNAs and miRNAs). A multilayer analysis was then developed to identify multiple types of transcriptional aberrations associated with different stages of gastric cancer, including differentially expressed mRNAs, recurrent somatic mutations, and key differentially expressed miRNAs. Through this approach, we identified the central metabolic regulator AMP-activated protein kinase (AMPK)α as a potential functional target in Asian gastric cancer. Furthermore, we experimentally showed the translational relevance of this gene as a potential therapeutic target for early-stage gastric cancer in Asian patients. Together, our findings not only provide a valuable information resource for identifying and elucidating the molecular mechanisms of Asian gastric cancer, but also represent a general integrative framework to develop more effective therapeutic targets.

PMID:
22434430
PMCID:
PMC3872998
DOI:
10.1158/0008-5472.CAN-11-3870
[Indexed for MEDLINE]
Free PMC Article

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