The study results, published in the May 5, 2016 online issue of Cell Reports, were reported by a team led by Gordon Mills, Ph.D., chair of Systems Biology at The University of Texas MD Anderson Cancer Center.
“MicroRNAs appear to have evolved to regulate cellular functions through having many different targets, and were thought to function mainly through down regulating the levels or functions of messenger RNA,” said Mills. “Remarkably, this study shows that microRNAs can also up regulate the expression of key cancer genes directly. This suggests that the mechanisms by which microRNAs regulate cellular function are much broader than was generally accepted.”
The team, using data from The Cancer Genome Atlas, zeroed in on the biochemical interplay between a transcription factor, STAT3, which has been associated with poor outcome in ovarian cancer patients when present in high levels, and a microRNA called miR551b. This little-studied microRNA now has been shown to impact STAT3 protein levels, contributing to resistance to cell death and increased proliferation of cancer cells both in vivo and in vitro. Mills believes this points to miR551b as a “promising candidate biomarker and therapeutic target.”
“The study supports the concept that targeting miR551b expression could block STAT3 activity, and prove useful for treating ovarian cancers,” said Mills. “We believe these findings warrant further evaluation of anti-miR therapies.”
To explore the potential of miR551b as a therapeutic target, Mills’ team treated mice with an anti-miR551b therapy, twice a week for a month and observed markedly decreased tumor growth.
“Our results demonstrate the therapeutic potential of anti-miR551b in treating ovarian cancers with high levels of miR551b,” said Mills. “Future studies will need to examine the activity of combination therapy of anti-miR551b with other therapeutic interventions.”