Abstract

Background99mTc-sestamibi single-photon emission computed tomography/computed tomography (SPECT/CT) has recently been explored for the characterization of indeterminate renal masses. As judged by increased intra-tumoral radiotracer uptake, we have previously reported the excellent diagnostic performance characteristics of this test for identifying benign/indolent oncocytomas and hybrid oncocytic/chromophobe tumors (HOCTs). In this study, we investigated potential molecular mechanisms underlying the discriminatory ability of 99mTc-sestamibi SPECT/CT for renal masses.Fifty renal masses imaged with 99mTc-sestamibi SPECT/CT prior to surgical resection were evaluated by immunohistochemistry for mitochondrial content and expression of the multi-drug resistance pump 1 (MDR1/P-gp). Immunohistochemical staining was scored semi-quantitatively, and results were compared across renal tumor histologies and correlated with 99mTc-sestamibi uptake.ResultsIn total, 6/6 (100%) and 2/2 (100%) HOCTs demonstrated strong mitochondrial content staining combined with low MDR1 staining. Clear cell renal cell carcinoma showed an opposite pattern with the majority having low mitochondrial (14/26, 54%) and high MDR1 staining (18/26, 69%). Other tumor types were more variable in staining pattern, although the staining pattern reliably predicted 99mTc-sestamibi uptake in almost all tumors except chromophobe renal cell carcinoma.ConclusionsOur findings confirm that renal tumors with high mitochondrial content and relatively low MDR pump expression activity accumulate 99mTc-sestamibi and allow for the accurate diagnosis of the benign/indolent tumor class that includes oncocytomas and HOCTs. For masses in which MDR activity outweighs the presence of mitochondria, the tumors appear cold on 99mTc-sestamibi SPECT/CT, allowing for high confidence in the diagnosis of renal cell carcinoma.

Highlights

  • The incidence of small renal masses has increased steadily in recent decades [1]

  • We examined the proposed mechanism of 99mTc-sestamibi uptake by renal tumors through immunohistochemical analysis of mitochondrial content and expression of multi-drug resistance (MDR) protein 1 (MDR1/P-gp) in a series of 50 renal masses imaged with 99mTc-sestamibi single-photon emission computed tomography (SPECT)/computed tomography (CT) prior to surgical resection

  • The degree of 99mTc-sestamibi uptake in indeterminate renal masses is dictated by an interplay between the presence of mitochondria and MDR pumps

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Summary

Introduction

The incidence of small renal masses has increased steadily in recent decades [1]. Despite this trend, there has not been a corresponding decrease in the number of newly diagnosed cases of metastatic renal cell carcinoma (RCC) [1,2,3]. There has not been a corresponding decrease in the number of newly diagnosed cases of metastatic renal cell carcinoma (RCC) [1,2,3] This discrepancy is at least partially a result of the over-treatment of benign and indolent tumors, with an estimated 5600 masses resected annually for the false presumption of cancer in the USA alone [4]. Imaging with 2deoxy-2-[18F]fluoro-D-glucose (FDG) positron emission tomography has failed to show utility in differentiating between the various renal tumor histologies [7, 8]

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