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Published on: January 31, 2025
Expression of vitamin D3 receptor in kidney tumors
Wenhua Liu1, Maria Tretiakova, Juan Kong
1Department of Pathology, The University of Chicago Hospitals, University of Chicago, 5841 S. Maryland Avenue, Chicago, IL 60637, USA.
Abstract:
The kidney is not only a primary vitamin D target organ but also is a key site of vitamin D metabolism. Recent studies have shown that vitamin D has important physiologic effects on proliferation and differentiation in a variety of benign and malignant cells. Our preliminary immunohistochemical study showed that vitamin D receptor (VDR) was highly expressed in renal distal tubules and collecting ducts, whereas the renal proximal tubules and glomeruli did not express VDR. These observations led us to study the expression of VDR in various kidney tumors to determine the possible diagnostic utility of VDR. Paraffin tissue microarray (TMA) blocks were constructed containing core cylinders from clear cell (52), papillary (35), chromophobe (20), sarcomatoid (20), and metastatic (59) renal cell carcinomas (RCCs). Oncocytomas (20), normal adult kidneys (12), and normal adult adrenals (6) were also included. In addition, 30 clear cell RCCs and 3 collecting duct carcinomas were also studied using conventional sections. Furthermore, VDR messenger RNA and protein expression was also quantified using real-time reverse transcriptase-polymerase chain reaction and Western blot analysis. Vitamin D receptor was strongly positive in collecting duct carcinomas (100% [3/3], cytoplasmic), papillary RCCs (94% [33/35], cytoplasmic), chromophobe RCCs (85% [17/20], membranous), and oncocytomas (90% [18/20], cytoplasmic with perinuclear accentuation). In contrast, VDR expression was focal/weak and present only in the peripheral regions of clear cell RCCs. Vitamin D receptor was weakly positive in sarcomatoid variant RCCs (88% [14/16]) regardless of the type of associated original RCC. Overall, VDR is a discriminative marker for renal cell tumors. The preferential expression of VDR in chromophobe RCCs, oncocytomas, and collecting duct carcinomas is in agreement with the concept that these tumors differentiate toward epithelium lining the distal convoluted tubules and collecting ducts. Considering the different VDR expression patterns, VDR is a useful ancillary tool in distinguishing chromophobe RCCs from oncocytomas. In addition, the focal and much weaker VDR expression in clear cell RCCs makes VDR valuable in distinguishing clear cell RCC from other types of RCCs.
Insights
Vitamin D receptor (VDR) expression differs across kidney tumor types. VDR is a valuable diagnostic marker, particularly for distinguishing clear cell renal cell carcinoma from other subtypes.
Area of Science:
- Nephrology
- Oncology
- Molecular Biology
Background:
- The kidney is a key site for vitamin D metabolism and a target organ for its actions.
- Vitamin D influences cell proliferation and differentiation in various cancers.
- Preliminary studies indicated vitamin D receptor (VDR) expression in specific kidney tubules.
Purpose of the Study:
- To investigate VDR expression patterns in different types of renal cell carcinomas (RCCs) and related tumors.
- To evaluate the diagnostic utility of VDR as a biomarker in kidney tumors.
Main Methods:
- Tissue microarrays and conventional sections of various RCC subtypes, oncocytomas, and normal kidney/adrenal tissues were analyzed for VDR expression.
- VDR messenger RNA and protein levels were quantified using real-time RT-PCR and Western blot analysis.
Main Results:
- Strong VDR expression was observed in collecting duct carcinomas, papillary RCCs, chromophobe RCCs, and oncocytomas.
- Clear cell RCCs exhibited focal and weaker VDR expression, primarily in peripheral regions.
- Sarcomatoid variant RCCs showed weak VDR positivity.
Conclusions:
- Vitamin D receptor serves as a discriminative marker for renal cell tumors.
- Preferential VDR expression in certain RCC subtypes aligns with their differentiation towards distal tubule/collecting duct epithelium.
- VDR expression patterns aid in differentiating between chromophobe RCC, oncocytoma, and clear cell RCC.
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