CLINICAL VALIDATION OF THE INFLUENCE OF P-GLYCOPROTEIN ON TECHNETIUM-99M-SESTAMIBI UPTAKE IN MALIGNANT-TUMORS

Citation
L. Kostakoglu et al., CLINICAL VALIDATION OF THE INFLUENCE OF P-GLYCOPROTEIN ON TECHNETIUM-99M-SESTAMIBI UPTAKE IN MALIGNANT-TUMORS, The Journal of nuclear medicine, 38(7), 1997, pp. 1003-1008
Citations number
22
Categorie Soggetti
Radiology,Nuclear Medicine & Medical Imaging
ISSN journal
01615505
Volume
38
Issue
7
Year of publication
1997
Pages
1003 - 1008
Database
ISI
SICI code
0161-5505(1997)38:7<1003:CVOTIO>2.0.ZU;2-9
Abstract
We prospectively studied 48 patients with either breast cancer (30 pat ients) or lung cancer (18 patients) to ascertain the relationship betw een the degree of accumulation of Tc-99m-sestamibi and the expression of p-glycoprotein in tumor tissues. Methods: During initial presentati on (37 patients) or post-therapy evaluation (11 patients), the patient s underwent contemporaneous Tc-99m-sestamibi imaging and biopsy (30 pa tients) or surgery (18 patients). The interval between surgery/biopsy and imaging Varied between 3 and 15 days. All patients had radiologica lly detectable tumors. Immunohistochemical studies were performed on p araffin sections using a monoclonal antibody, JSB-1, developed against the internal epitope of p-glycoprotein. Tumor-to-background ratios we re correlated with the level of p-glycoprotein expression determined b y immunohistochemical studies. Results: Our results showed an inverse correlation between the tumor-to-background ratios of Tc-99m-sestamibi and the density of p-glycoprotein expression in tumor tissues. The va lues for the tumor-lo-background ratios were significantly lower for t hose tumors expressing p-glycoprotein at high levels than those with s cattered and no expression (p < 0.01 and p < 0.001, respectively). Con clusion: Although our results warrant further studies at the molecular revel using PCR techniques after the extraction of mRNA, our data str ongly suggest that Tc-99m-sestamibi imaging is useful to noninvasively determine the presence of multidrug resistance in patients with malig nant tumors.