Haemoprotection against cytostatic drugs by stem cell inhibition
Autor: | Walter R. Paukovits, Marie-Hélène Moser |
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Rok vydání: | 1991 |
Předmět: |
Pharmacology
Chemotherapy Necrosis medicine.medical_treatment Antineoplastic Agents Neutropenia Biology Toxicology medicine.disease Hematopoietic Stem Cells Hematologic Diseases Haematopoiesis medicine.anatomical_structure Immunology medicine Cancer research Animals Humans Bone marrow Stem cell medicine.symptom Macrophage inflammatory protein Transforming growth factor |
Zdroj: | Trends in pharmacological sciences. 12(8) |
ISSN: | 0165-6147 |
Popis: | Cytostatic drug-induced haematopoietic damage is a major problem in tumour chemotherapy, due to the intensive proliferation of many bone marrow constituents and to the drug-induced recruitment of immature pluripotent haematopoietic cells (spleen colony-forming units, CFU-S). Marie-Helene Moser and Walter Paukovits discuss how it should be possible to minimize such proliferation-associated damage by inhibiting CFU-S during the most dangerous treatment phases, with factors such as transforming growth factor β, tumour necrosis factor α, macrophage inflammatory protein 1α, and the CFU-S-inhibitory peptides N -acetyl-Ser-Asp-Lys-Pro and pyroGlu-Glu-Asp-Cys-Lys (pEEDCK). Clinically relevant data are available for pEEDCK, showing that application of this peptide leads to a delayed, shorter, and less severe neutropenia, combination of pEEDCK with a stimulator avoids neutropenia, and stem cell preservation with pEEDCK improves long-term reconstitution of the haematopoietic system. Stem cell inhibition by synthetic peptides like pEEDCK may provide a useful strategy for bone marrow protection. |
Databáze: | OpenAIRE |
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