The clinical relevance of the expression of several multidrug-resistant-related genes in patients with primary acute myeloid leukemia
- PMID: 12962366
- DOI: 10.1179/joc.2003.15.4.374
The clinical relevance of the expression of several multidrug-resistant-related genes in patients with primary acute myeloid leukemia
Abstract
Multidrug resistance (MDR) is a complex phenomenon that includes the expression of many different genes regulating drug transport or metabolism, cellular repair or detoxification mechanisms. The co-expression of several genes could be at the basis of the resistant phenotype in vivo. In order to test a possible prognostic role of the expression and co-expression of several MDR-related genes (MDR1, topoisomerase IIalpha, topoisomerase IIbeta, MRP, GSTpi, LRP), 35 patients affected by acute myeloid leukemia (AML) were tested by RT-PCR assays. In our series, topoisomerase IIbeta was significantly co-expressed with MRP (p = 0.05), GSTpi (p = 0.017) and LRP (p = 0.005). GSTpi was co-expressed with LRP (p = 0.03) and MRP (p = 0.007); on the other hand, 53.8% of patients were LRP and MRP-positive (p = 0.02). The PCR-positivity did not differ according to biological/clinical characteristics of patients, including age; this latter was the only parameter conditioning the response and overall survival. Neither the expression nor the co-expression of the tested genes was significantly correlated with the response to the induction treatment and long-term outcome.
Similar articles
-
[The clinical significance of lung resistance-related protein gene (lrp), multidrug resistance-associated protein gene (mrp) and mdr-1/p170 expression in acute leukemia].Zhonghua Nei Ke Za Zhi. 1999 Nov;38(11):760-3. Zhonghua Nei Ke Za Zhi. 1999. PMID: 11798719 Chinese.
-
FLT3-ITD and MLL-PTD influence the expression of MDR-1, MRP-1, and BCRP mRNA but not LRP mRNA assessed with RQ-PCR method in adult acute myeloid leukemia.Ann Hematol. 2014 Apr;93(4):577-93. doi: 10.1007/s00277-013-1898-7. Epub 2013 Sep 13. Ann Hematol. 2014. PMID: 24030729 Clinical Trial.
-
Prognostic significance of multidrug resistance gene 1 (MDR1), multidrug resistance-related protein (MRP) and lung resistance protein (LRP) mRNA expression in acute leukemia.J Korean Med Sci. 2006 Apr;21(2):253-8. doi: 10.3346/jkms.2006.21.2.253. J Korean Med Sci. 2006. PMID: 16614510 Free PMC article.
-
Multiple drug resistance protein (MDR-1), multidrug resistance-related protein (MRP) and lung resistance protein (LRP) gene expression in childhood acute lymphoblastic leukemia.Sao Paulo Med J. 2004 Jul 1;122(4):166-71. doi: 10.1590/s1516-31802004000400007. Epub 2004 Nov 9. Sao Paulo Med J. 2004. PMID: 15543372 Free PMC article. Review.
-
Assessment of drug resistance in acute myeloid leukemia.Expert Rev Mol Diagn. 2004 Sep;4(5):705-13. doi: 10.1586/14737159.4.5.705. Expert Rev Mol Diagn. 2004. PMID: 15347263 Review.
Cited by
-
Increased expression of cdc2 inhibits transport function of RLIP76 and promotes apoptosis.Cancer Lett. 2009 Oct 8;283(2):152-8. doi: 10.1016/j.canlet.2009.03.033. Epub 2009 Apr 17. Cancer Lett. 2009. PMID: 19375851 Free PMC article.
-
Radiation- and chemoinduced multidrug resistance in colon carcinoma cells.Strahlenther Onkol. 2009 Dec;185(12):815-20. doi: 10.1007/s00066-009-1993-9. Strahlenther Onkol. 2009. PMID: 20013091
-
Effects of Hypoxia on Biology of Human Leukemia T-cell Line (MOLT-4 cells) Co-cultured with Bone Marrow Mesenchymal Stem Cells.Avicenna J Med Biotechnol. 2018 Apr-Jun;10(2):62-68. Avicenna J Med Biotechnol. 2018. PMID: 29849981 Free PMC article.
-
The potential biomarkers in predicting pathologic response of breast cancer to three different chemotherapy regimens: a case control study.BMC Cancer. 2009 Jul 11;9:226. doi: 10.1186/1471-2407-9-226. BMC Cancer. 2009. PMID: 19591668 Free PMC article.
-
Prognostic impact of multidrug resistance gene expression on the management of breast cancer in the context of adjuvant therapy based on a series of 171 patients.Br J Cancer. 2006 Feb 27;94(4):473-80. doi: 10.1038/sj.bjc.6602958. Br J Cancer. 2006. PMID: 16434992 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous