Ys. Kim et al., Tc-99m MIBI SPECT is useful for noninvasively predicting the presence of MDR1 gene-encoded P-glycoprotein in patients with hepatocellular carcinoma, CLIN NUCL M, 24(11), 1999, pp. 874-879
Purpose: Resistance to chemotherapeutic drugs continues to be one of the ma
jor unsolved problems in the treatment of cancer. Multidrug resistance is d
efined as the ability of cells exposed to a single drug to develop resistan
ce to a broad range of structurally and functionally unrelated drugs as a r
esult of enhanced outward transport of drugs mediated by P-glycoprotein tha
t is encoded by multidrug resistance genes. Recent evidence has shown that
Tc-99m MIBI is a suitable transport substrate for P-glycoprotein. A potenti
al advantage of Tc-99m MIBI SPECT is its superiority to diagnose noninvasiv
ely the presence of P-glycoprotein overexpression in vivo. In this study, t
he authors determined the association of enhanced MIBI efflux in Tc-99m MIB
I SPECT with overexpression of P-glycoprotein in hepatocellular carcinoma.
Materials and Methods: Thirty-five patients with hepatocellular carcinoma w
ere enrolled in the study. Tc-99m MIBI SPECT was performed 10 minutes after
intravenous injection of 20 mCi Tc-99m MIBI. All patients had liver biopsy
or surgery within 1 week of MIBI imaging. Immunohistochemical study of the
biopsy or resected hepatocellular carcinoma specimens was performed using
the avidin-biotin-peroxidase technique with monoclonal antibody JSB-1 direc
ted against P-glycoprotein.
Results: On Tc-99m MIBI SPECT, 30 of 35 (85.7%) patients with hepatocellula
r carcinoma had no Tc-99m MIBI uptake in tumor lesions, whereas five patien
ts with hepatocellular carcinoma had Tc-99m MIBI uptake in tumor lesions. P
-glycoprotein expression was observed in tumor tissues of all the patients
without Tc-99m MIBI uptake, whereas among the five patients with Tc-99m MIB
I uptake, no P-glycoprotein expression was seen in tumor lesions (P < 0.015
).
Conclusion: Tc-99m MIBI SPECT is useful for noninvasively predicting the pr
esence of MDR1 gene-encoded P-glycoprotein in patients with hepatocellular
carcinoma.