IMP3, a Promising Prognostic Marker in Clear Cell Renal Cell Carcinoma
Insulin-like growth factor II mRNA-binding protein 3 (IMP3) has been reported as a prognostic biomarker in various cancers. To validate IMP3 as a prognostic biomarker in renal cell carcinoma (RCC), we investigated the expression of IMP3, p53, and Ki-67, and their associations with clinicopathologic...
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Published in: | Journal of pathology and translational medicine Vol. 48; no. 2; pp. 108 - 116 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Korea (South)
Korean Society of Pathologists, Korean Society for Cytopathology
01-04-2014
The Korean Society of Pathologists and The Korean Society for Cytopathology 대한병리학회 |
Subjects: | |
Online Access: | Get full text |
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Summary: | Insulin-like growth factor II mRNA-binding protein 3 (IMP3) has been reported as a prognostic biomarker in various cancers. To validate IMP3 as a prognostic biomarker in renal cell carcinoma (RCC), we investigated the expression of IMP3, p53, and Ki-67, and their associations with clinicopathologic outcomes.
We studied 148 clear cell RCCs (CCRCCs) from patients who underwent radical nephrectomy. The expression levels of IMP3, p53, and Ki-67 were assessed by immunohistochemical staining and the clinical and pathologic parameters were retrospectively reviewed.
Twenty-nine percent of CCRCCs expressed IMP3. Forty-one percent of IMP3-immunopositive tumors developed metastases, while only 11.4% of IMP3-negative tumors developed metastases (p<.001). A Kaplan-Meier curve showed that patients with IMP3-immunopositive tumors had lower metastasis-free survival and cancer-specific survival than did those with IMP3-immunonegative tumors (p<.001 and p<.001, respectively). Expression of high Ki-67 proliferation index was also associated with a higher metastatic rate. In the multivariate Cox regression analysis, pT stage and IMP3-positivity were independently associated with disease-specific survival.
IMP3 is an independent prognostic biomarker for patients with CCRCC to predict metastasis and poor outcome. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 G704-000333.2014.48.2.011 |
ISSN: | 1738-1843 2383-7837 2092-8920 2383-7845 |
DOI: | 10.4132/KoreanJPathol.2014.48.2.108 |