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Loss of miR‐101 expression promotes Wnt/β‐catenin signalling pathway activation and malignancy in colon cancer cells
Authors:Antonio Strillacci  Maria Chiara Valerii  Pasquale Sansone  Cinzia Caggiano  Annamaria Sgromo  Laura Vittori  Michelangelo Fiorentino  Gilberto Poggioli  Fernando Rizzello  Massimo Campieri  Enzo Spisni
Affiliation:1. Department of Biology, University of Bologna, , Italy;2. Department of Clinical Medicine, St. Orsola‐Malpighi Hospital, , Bologna, Italy;3. Department of Medicine, Memorial Sloan Kettering Cancer Center, , New York, NY, USA;4. Centre for Applied Biomedical Research (CRBA), St. Orsola‐Malpighi Hospital, , Bologna, Italy;5. Pathology Unit, Addarii Institute of Oncology, St. Orsola‐Malpighi Hospital, , Bologna, Italy
Abstract:
Colorectal cancer (CRC) is the second leading cause of cancer‐related mortality in Western countries. Although the aberrant expression of several microRNAs (oncomiRs) is associated with CRC progression, the molecular mechanisms of this phenomenon are still under investigation. Here we show that miR‐101 expression is differentially impaired in CRC specimens, depending on tumour grade. miR‐101 re‐expression suppresses cell growth in 3D, hypoxic survival and invasive potential in CRC cells showing low levels of miR‐101. Additionally, we provide molecular evidence of a bidirectional regulatory mechanism between miR‐101 expression and important CRC pro‐malignant features, such as inflammation, activation of the Wnt/β‐catenin signalling pathway and epithelial–mesenchymal transition (EMT). We then propose that up‐regulated miR‐101 may function as a tumour suppressor in CRC and that its pharmacological restoration might hamper the aggressive behaviour of CRC in vivo. MiR‐101 expression may also represent a cancer biomarker for CRC diagnosis and prognosis. Copyright © 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
Keywords:Colorectal cancer  MiR‐101  β  ‐catenin  hypoxia  EMT  inflammation
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