Korean J Urol.  1996 Apr;37(4):392-400.

Multidrug Resistance-Related Gene Expressions in Germ Cell Tumors in Testis

Affiliations
  • 1Department of Urology, Chungbuk National University, Cheongju, Korea.

Abstract

The development of drug resistance is a major obstacle in effective cancer chemotherapy. Multidrug resistance(MDR) is a widely studied phenomenon of interest to both clinicians and research workers because many different cancer chemotherapeutic agents are involved and the genetic basis of MDR is understood to a large extent. Several studies show that the P-glycoprotein (P-gp), multidrug resistance-associated protein(MRP), glutathione-s-transferase-pi(GST-pi), and DNA topoisomerase II(topo II) have a complex role for the malignant phenotypes and MDR. Clearly, there is a need to investigate links between the diverse characteristics of tumors and the emergence of drug resistance. We have therefore used reverse transcription-polymerase chain reaction(RT-PCR) assay to analyze expressions of MDR-related genes including the mdr1, MRP, topo II and GST-t gene in normal testis and testis tumors. The results are as follows: 1. The expression levels of topo II and GST-n genes in testis tumors, especially in the nonseminomatous germ cell tumor(NSGCT), were significantly higher than in normal testis(p=0.015 and 0.025, respectively). 2. The MDR-related gene expressions in testis tumors did not appear to be correlated with stage(p>0.05 in each case) and chemotherapy status(p>0.05 in each case). 3. MRP expression levels in primary tumors were much higher than in metastatic tumors. 4. In NSGCT, the coexpressions of the topo II and GST-r or MRP genes were significantly correlated but, seminoma showed no correlation between MDR-related genes in the same sample. Although the mechanism of these connection are not known, the results suggest that these expression patterns and higher GST-rexpression in NSGCF compared to seminoma confer diverse characteristics including difference in the presentation of tumor markers and the responsiveness to chemotherapy on NSGCF and seminoma.

Keyword

mdr1; MRP; GST-pi; DNA topoisomerase II

MeSH Terms

DNA Topoisomerases, Type I
DNA Topoisomerases, Type II
Drug Resistance
Drug Therapy
Gene Expression*
Germ Cells*
Neoplasms, Germ Cell and Embryonal*
P-Glycoprotein
Phenotype
Seminoma
Testis*
Biomarkers, Tumor
DNA Topoisomerases, Type I
DNA Topoisomerases, Type II
P-Glycoprotein
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