Stromal expression of microRNA-21 in advanced colorectal cancer patients with distant metastases

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Abstract

Background: The aim of this study was to determine the regional heterogeneity and clinicopathological significance of microRNA-21 (miR-21) in advanced colorectal cancer (CRC) patients with distant metastasis. Methods: miR-21 expression was investigated by using locked nucleic acid- fluorescence in situ hybridization in the center and periphery of the primary cancer and in distant metastasis from 170 patients with advanced CRC. In addition, α-smooth muscle actin and desmin were evaluated to identify cancer-associated fibroblasts (CAFs) by using immunohistochemistry. Results: The miR-21 signal was observed in the cancer stroma. The expression of miR-21 (a score of 1-4) in the center and periphery of the primary cancer and in distant metastasis was observed in specimens from 133 (78.2%), 105 (61.8%), and 91 (53.5%) patients, respectively. miR-21 expression was heterogeneous in advanced CRC. Discordance between miR-21 expression in the center of the primary cancer and either the periphery of the primary cancer or distant metastasis was 31.7% or 44.7%, respectively. miR-21 stromal expression in the periphery of the primary cancer was significantly associated with a better prognosis (p = .004). miR-21 expression was significantly associated with CAFs in the center of the primary cancer (p = .001) and distant metastases (p = .041). Conclusions: miR-21 expression is observed in cancer stroma related to the CAF quantity and frequently presents regional heterogeneity in CRC. Our findings indicate that the role of miR-21 in predicting prognosis may be controversial but provide a new perspective of miR-21 level measurement in cancer specimens.

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Lee, K. S., Nam, S. K., Koh, J., Kim, D. W., Kang, S. B., Choe, G., … Lee, H. S. (2016). Stromal expression of microRNA-21 in advanced colorectal cancer patients with distant metastases. Journal of Pathology and Translational Medicine, 50(4), 270–277. https://doi.org/10.4132/jptm.2016.03.19

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