The loss or silencing of these genes, which are called mismatch repair genes, causes inherited cancer-susceptibility syndromes and contributes to the progression of colorectal, uterine, ovarian and other cancers.
"Our findings suggest that miR-155 expression might be an important stratification factor in the prognosis and treatment of cancer patients," says Dr. Carlo M. Croce, from Ohio State's Human Cancer Genetics program.
The study found that overexpression of miR-155 reduced the expression of the human mismatch repair genes MLH1, MSH2 and MSH6 by 72 percent, 42 percent and 69 percent, respectively, in a colorectal cancer cell line. The results also showed that high expression of miR-155 in human colorectal tumors correlates with low expression of MLH1 and MSH2. Further, human tumors that feature unexplained mismatch repair inactivation showed miR-155 overexpression.
The third finding may explain a colon-cancer conundrum. About five percent of colorectal cancer cases feature a genomic marker called microsatellite instability that signals the loss of mismatch repair ability and the presence of an inherited cancer predisposition condition. These cases also show no expression of mismatch genes. Yet, the genes themselves show no alterations that explain the loss of expression.
"This study describes a totally new mechanism that might explain those cases of colorectal cancer that display microsatellite instability but no mutations or epigenetic inactivation of the mismatch repair genes," says co-author Muller Fabbri, a research scientist with the OSUCCC-James.
Citation: Valeri et al., 'Modulation of mismatch repair and genomic stability by miR-155', PNAS 2010, 107 (15) 6982-6987; doi:10.1073/pnas.1002472107