Literature DB >> 8254825

Effect of glutathione and its related enzymes on chemosensitivity of renal cell carcinoma and bladder carcinoma cell lines.

H Ahn1, E Lee, K Kim, C Lee.   

Abstract

Glutathione and glutathione-related enzymes have been implicated in sensitivity of tumors to chemotherapeutic drugs. In the present study, glutathione and the activity of its related enzymes were quantitated in 4 renal cell carcinoma cell lines and 4 bladder carcinoma cell lines. The expression of glutathione-s-transferase pi and alpha in each cell line was analyzed by immunoblot analysis. The relationships between glutathione levels, glutathione peroxidase activity and glutathione-s-transferase activity and tumor sensitivity to cisplatinum, doxorubicin and vinblastine were determined by linear regression analysis. Glutathione levels were positively related to cisplatinum resistance in both renal cell carcinoma and bladder carcinoma cell lines and to doxorubicin resistance in bladder carcinoma cell lines. A positive correlation between glutathione peroxidase activity and doxorubicin resistance was identified in renal cell carcinoma cell lines, but no correlation was noted in bladder carcinoma cell lines. No significant correlation was apparent between glutathione-s-transferase activity and sensitivity to any of the drugs tested in this study. To further clarify the relationship between glutathione levels and the cytotoxicity of the drugs, we evaluated the effect of glutathione depletion by L-buthionine sulfoximine on the cytotoxicity of the drugs in bladder carcinoma cell lines. Glutathione depletion enhanced cisplatinum cytotoxicity 1.3- to 1.7-fold and doxorubicin cytotoxicity by 1.45- to 11.2-fold. Glutathione depletion did not change vinblastine cytotoxicity. The present study demonstrates that glutathione and its related enzymes affect sensitivity to cisplatinum or doxorubicin. The drug resistance mechanism elicited by glutathione and its related enzymes in these tumors needs further elucidation so that chemotherapeutic regimens may be modified.

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Year:  1994        PMID: 8254825     DOI: 10.1016/s0022-5347(17)34929-7

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  6 in total

1.  Expression of xenobiotic metabolizing enzymes in tumours of the urinary bladder.

Authors:  G I Murray; V E Taylor; J A McKay; R J Weaver; S W Ewen; W T Melvin; M D Burke
Journal:  Int J Exp Pathol       Date:  1995-08       Impact factor: 1.925

2.  Patterns of Expression of H2S-Producing Enzyme in Human Renal Cell Carcinoma Specimens: Potential Avenue for Future Therapeutics.

Authors:  Emrullah Sogutdelen; Katharine Pacoli; Smriti Juriasingani; Masoud Akbari; Manal Gabril; Alp Sener
Journal:  In Vivo       Date:  2020 Sep-Oct       Impact factor: 2.155

3.  NMR studies of the relationship between the changes of membrane lipids and the cisplatin-resistance of A549/DDP cells.

Authors:  Zhenhua Huang; Yufeng Tong; Jinfeng Wang; Youguo Huang
Journal:  Cancer Cell Int       Date:  2003-04-08       Impact factor: 5.722

4.  Glutathione-S-transferase-pi (GST-pi) expression in renal cell carcinoma.

Authors:  Christina Kaprilian; Maria Horti; Kosmas Kandilaris; Andreas Skolarikos; Nikolaos Trakas; Ioannis Kastriotis; Charalambos Deliveliotis
Journal:  J Kidney Cancer VHL       Date:  2015-02-22

5.  Increased H2S and its synthases in urothelial cell carcinoma of the bladder, and enhanced cisplatin-induced apoptosis following H2S inhibition in EJ cells.

Authors:  Wasilijiang Wahafu; Junwei Gai; Liming Song; Hao Ping; Mingshuai Wang; Feiya Yang; Yinong Niu; Nianzeng Xing
Journal:  Oncol Lett       Date:  2018-03-29       Impact factor: 2.967

Review 6.  Hydrogen Sulfide: Emerging Role in Bladder, Kidney, and Prostate Malignancies.

Authors:  Masoud Akbari; Emrullah Sogutdelen; Smriti Juriasingani; Alp Sener
Journal:  Oxid Med Cell Longev       Date:  2019-11-03       Impact factor: 6.543

  6 in total

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