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miRNA Expression in Colon Polyps Provides Evidence for a Multihit Model of Colon Cancer

Overview of attention for article published in PLOS ONE, June 2011
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Title
miRNA Expression in Colon Polyps Provides Evidence for a Multihit Model of Colon Cancer
Published in
PLOS ONE, June 2011
DOI 10.1371/journal.pone.0020465
Pubmed ID
Authors

Ann L. Oberg, Amy J. French, Aaron L. Sarver, Subbaya Subramanian, Bruce W. Morlan, Shaun M. Riska, Pedro M. Borralho, Julie M. Cunningham, Lisa A. Boardman, Liang Wang, Thomas C. Smyrk, Yan Asmann, Clifford J. Steer, Stephen N. Thibodeau

Abstract

Changes in miRNA expression are a common feature in colon cancer. Those changes occurring in the transition from normal to adenoma and from adenoma to carcinoma, however, have not been well defined. Additionally, miRNA changes among tumor subgroups of colon cancer have also not been adequately evaluated. In this study, we examined the global miRNA expression in 315 samples that included 52 normal colonic mucosa, 41 tubulovillous adenomas, 158 adenocarcinomas with proficient DNA mismatch repair (pMMR) selected for stage and age of onset, and 64 adenocarcinomas with defective DNA mismatch repair (dMMR) selected for sporadic (n = 53) and inherited colon cancer (n = 11). Sporadic dMMR tumors all had MLH1 inactivation due to promoter hypermethylation. Unsupervised PCA and cluster analysis demonstrated that normal colon tissue, adenomas, pMMR carcinomas and dMMR carcinomas were all clearly discernable. The majority of miRNAs that were differentially expressed between normal and polyp were also differentially expressed with a similar magnitude in the comparison of normal to both the pMMR and dMMR tumor groups, suggesting a stepwise progression for transformation from normal colon to carcinoma. Among the miRNAs demonstrating the largest fold up- or down-regulated changes (≥4), four novel (miR-31, miR-1, miR-9 and miR-99a) and two previously reported (miR-137 and miR-135b) miRNAs were identified in the normal/adenoma comparison. All but one of these (miR-99a) demonstrated similar expression differences in the two normal/carcinoma comparisons, suggesting that these early tumor changes are important in both the pMMR- and dMMR-derived cancers. The comparison between pMMR and dMMR tumors identified four miRNAs (miR-31, miR-552, miR-592 and miR-224) with statistically significant expression differences (≥2-fold change).

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 92 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 92 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 24 26%
Student > Ph. D. Student 21 23%
Student > Bachelor 10 11%
Student > Master 7 8%
Professor > Associate Professor 5 5%
Other 13 14%
Unknown 12 13%
Readers by discipline Count As %
Agricultural and Biological Sciences 35 38%
Biochemistry, Genetics and Molecular Biology 20 22%
Medicine and Dentistry 17 18%
Pharmacology, Toxicology and Pharmaceutical Science 2 2%
Nursing and Health Professions 1 1%
Other 5 5%
Unknown 12 13%