Mesothelin, a possible target for immunotherapy, is expressed in primary AML cells
- 21 July 2007
- journal article
- Published by Wiley in European Journal of Haematology
- Vol. 79 (4) , 281-286
- https://doi.org/10.1111/j.1600-0609.2007.00928.x
Abstract
Mesothelin is a promising candidate for tumor-specific therapy because of its limited expression in normal tissues and high expression in several cancers. The expression of the protein mesothelin in hematological malignancies has not yet been analyzed. SS1(dsFv)PE38 is a recombinant anti-mesothelin immunotoxin which is undergoing clinical evaluation in patients with mesothelin-expressing tumors. In this study we show that the mesothelin protein is expressed in leukemic cells from children with acute myeloid leukemia (AML). This finding was confirmed by western blot, immunocytochemistry and real time polymerase chain reaction (PCR). Despite the expression of mesothelin, the patient samples were not sensitive to immunotoxin SS1(dsFv)PE38 in MTT assays. Primary AML cells express mesothelin but SS1(dsFv)PE38 is not active in killing these cells. Other approaches that utilize mesothelin as a target might be more effective and should be tested against AML cells.Keywords
This publication has 12 references indexed in Scilit:
- New Immunotoxins Targeting CD123, a Stem Cell Antigen on Acute Myeloid Leukemia CellsJournal of Immunotherapy, 2007
- MESOMARK™: A Potential Test for Malignant Pleural MesotheliomaClinical Chemistry, 2007
- Mesothelin Expression in Human Lung CancerClinical Cancer Research, 2007
- Less Toxicity by Optimizing Chemotherapy, but Not by Addition of Granulocyte Colony-Stimulating Factor in Children and Adolescents With Acute Myeloid Leukemia: Results of AML-BFM 98Journal of Clinical Oncology, 2006
- Mesothelin Is Shed from Tumor CellsCancer Epidemiology, Biomarkers & Prevention, 2006
- Identification of a Set of Seven Genes for the Monitoring of Minimal Residual Disease in Pediatric Acute Myeloid LeukemiaClinical Cancer Research, 2006
- The use of housekeeping genes for real-time PCR-based quantification of fusion gene transcripts in acute myeloid leukemiaLeukemia, 2004
- Enhancement of cytotoxicity of artemisinins toward cancer cells by ferrous ironFree Radical Biology & Medicine, 2004
- MesothelinClinical Cancer Research, 2004
- The multidrug resistance-associated protein 3 (MRP3) is associated with a poor outcome in childhood ALL and may account for the worse prognosis in male patients and T-cell immunophenotypeBlood, 2003