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MicroRNA expression patterns in adrenocortical carcinoma variants and clinical pathologic correlations
Eleonora Duregon1, Ida Rapa1, Arianna Votta1
1Department of Oncology, University of Turin at San Luigi Hospital, Orbassano, 10043, Torino, Italy.
Human Pathology
|June 4, 2014
Summary
MicroRNA (miRNA) expression differs across adrenocortical carcinoma (ACC) variants. High miR-210 levels correlate with aggressive features and poorer prognosis in ACC patients.
Area of Science:
- Endocrinology
- Oncology
- Molecular Biology
Background:
- MicroRNAs (miRNAs) are implicated in adrenocortical carcinoma (ACC) development.
- Limited data exists on miRNA expression in ACC histologic variants and their clinical correlation.
Purpose of the Study:
- To evaluate the expression of five selected miRNAs (miR-483-3p, miR-483-5p, miR-210, miR-195, miR-1974) in ACC histologic variants.
- To correlate miRNA expression with clinicopathologic features and prognostic markers.
Main Methods:
- Expression analysis of five miRNAs in 51 ACC samples (35 classical, 6 myxoid, 10 oncocytic).
- Comparison with clinical, pathological, and immunohistochemical data (steroidogenic factor 1, p53, β-catenin, glucose transporter 1, Ki-67).
- Statistical analysis including univariate and multivariate survival analyses.
Main Results:
- Oncocytic carcinomas showed reduced expression of miR-483-3p, miR-483-5p, and miR-210 compared to other histotypes.
- High miR-210 expression was linked to necrosis, elevated Ki-67 index, and increased glucose transporter 1.
- High miR-210 was associated with shorter overall survival, while high mitotic index was the sole independent prognostic factor.
Conclusions:
- miR-483-3p, miR-483-5p, and miR-210 exhibit differential expression in ACC variants.
- Elevated miR-210 levels are indicative of aggressive clinicopathologic parameters and portend a poorer prognosis in ACC.
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