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Monitoring treatment response of childhood acute lymphocytic leukemia with certain molecular and biochemical markers
- Source :
- Journal of Biochemical and Molecular Toxicology. 24:343-350
- Publication Year :
- 2010
- Publisher :
- Wiley, 2010.
-
Abstract
- Apoptosis is the primary mechanism through which most chemotherapeutic agents induce tumor cell death. The purpose of this study was to monitor the expression of pro- and anti-apoptotic proteins CD(95) , Bcl-2, as well as copper and zinc levels in the peripheral blood of children with acute lymphocytic leukemia (ALL) prior to and 6 months after the beginning of chemotherapy. Blood parameters and bone marrow blast count were also assessed. Twenty of 26 patients who received treatment showed amelioration in apoptotic response, which is reflected in the elevation of CD(95) , whereas Bcl-2 protein was significantly lowered. In these patients, the elevated serum copper level was not significantly affected whereas the low serum zinc level was significantly raised. Improvement in blood parameters and bone marrow blast count were also achieved. Taken together, the data suggested that assessment of apoptosis signaling molecules might have a predictive impact on treatment outcome.
- Subjects :
- Male
Treatment response
Health, Toxicology and Mutagenesis
medicine.medical_treatment
Apoptosis
Toxicology
Blast Count
Biochemistry
Acute lymphocytic leukemia
medicine
Humans
fas Receptor
Child
Molecular Biology
Chemotherapy
business.industry
Case-control study
General Medicine
Precursor Cell Lymphoblastic Leukemia-Lymphoma
medicine.disease
Fas receptor
Zinc
medicine.anatomical_structure
Proto-Oncogene Proteins c-bcl-2
Case-Control Studies
Immunology
Molecular Medicine
Female
Bone marrow
Apoptosis Regulatory Proteins
business
Biomarkers
Copper
Subjects
Details
- ISSN :
- 10956670
- Volume :
- 24
- Database :
- OpenAIRE
- Journal :
- Journal of Biochemical and Molecular Toxicology
- Accession number :
- edsair.doi.dedup.....733a6444db0a1ec83b27f957a9403003
- Full Text :
- https://doi.org/10.1002/jbt.20344