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Modeling Spontaneous Metastatic Renal Cell Carcinoma (mRCC) in Mice Following Nephrectomy
Published on: April 29, 2014
MET expression in sporadic renal cell carcinomas
Jong Sun Choi1, Mi-Kyung Kim, Jin Won Seo
1Department of Pathology, Cheil General Hospital, Samsung Medical Center, Sungkyunkwan University School of Medicine, Gangnam-gu, Seoul, Korea.
Abstract:
Although germline mutations of met proto-oncogene on human chromosome 7q31-34 have been known as useful molecular markers of hereditary papillary renal cell carcinoma (RCC), the expression of MET, a product of met proto-oncogene, has not been fully studied in sporadic RCC, along with its clinical significance. We investigated the expression of MET by immunohistochemistry in 182 cases of renal neoplasm encompassing 145 RCC, 25 urothelial carcinomas of renal pelvis, and 12 oncocytomas. MET was diffusely and strongly expressed in 90% of papillary RCC, all collecting duct carcinomas, and 92% of urothelial carcinomas of renal pelvis. On the contrary, clear cell RCC, chromophobe RCC, and oncocytomas were negative or focally positive for MET expression. In clear cell RCC, MET expression was positively correlated with high nuclear grade, presence of infiltrative growth, tumoral necrosis, papillary architecture, sarcomatoid component, tumoral involvement of the renal pelvis or ureter, involvement of the calyx, and lymphatic invasion. In conclusion, diffuse and strong expression of MET in papillary RCC and collecting duct carcinoma might be helpful in discriminating from the other subtypes of RCC with tubular or papillary growth. In case of MET expression observed in clear cell RCC, it might correlate with those clinicopathological parameters implying aggressive behavior.
Insights
The MET proto-oncogene is highly expressed in papillary and collecting duct renal cell carcinoma (RCC), aiding in diagnosis. MET expression in clear cell RCC indicates aggressive features.
Area of Science:
- Oncology
- Molecular Pathology
- Urologic Pathology
Background:
- Germline mutations in the MET proto-oncogene are established markers for hereditary papillary renal cell carcinoma (RCC).
- The expression and clinical significance of MET protein in sporadic RCC remain underexplored.
Purpose of the Study:
- To investigate the expression patterns of MET protein in various subtypes of renal neoplasms.
- To determine the clinical significance of MET expression in sporadic renal cell carcinoma, particularly clear cell RCC.
Main Methods:
- Immunohistochemistry was employed to assess MET expression.
- The study analyzed 182 cases, including 145 RCCs, 25 urothelial carcinomas of the renal pelvis, and 12 oncocytomas.
Main Results:
- Diffuse and strong MET expression was observed in 90% of papillary RCC, all collecting duct carcinomas, and 92% of urothelial carcinomas of the renal pelvis.
- Clear cell RCC, chromophobe RCC, and oncocytomas showed negative or focal MET expression.
- In clear cell RCC, MET expression correlated with high nuclear grade, infiltrative growth, necrosis, papillary architecture, sarcomatoid features, pelvic/ureteral involvement, calyceal involvement, and lymphatic invasion.
Conclusions:
- Diffused and strong MET expression can help differentiate papillary RCC and collecting duct carcinoma from other RCC subtypes with tubular or papillary growth.
- MET expression in clear cell RCC may serve as a biomarker for aggressive clinicopathological features.
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