The potent angioinhibin AGM-1470 stimulates normal but not human tumoral lymphocytes
Autor: | Ernst Heinen, Vincent Castronovo, Roberto Locigno, Nadine Antoine, Léon J. Simar, Marc Daukandt |
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Rok vydání: | 1996 |
Předmět: |
Drug
Cancer Research Lymphoma medicine.drug_class media_common.quotation_subject Antibiotics Lymphocyte Activation 030218 nuclear medicine & medical imaging Neovascularization 03 medical and health sciences 0302 clinical medicine In vivo Cyclohexanes medicine Tumor Cells Cultured Humans Fumagillin media_common O-(Chloroacetylcarbamoyl)fumagillol Antibiotics Antineoplastic Neovascularization Pathologic Cell growth Chemistry General Medicine medicine.disease Oncology Cell culture 030220 oncology & carcinogenesis Cancer research medicine.symptom Sesquiterpenes medicine.drug |
Zdroj: | Scopus-Elsevier |
ISSN: | 0300-8916 |
Popis: | Background AGM-1470 is a newly synthesized molecule developed as an analog of the potent anti-angiogenic fumagillin. Its efficacy in restraining tumor growth in vivo and the absence of major side effects have already led to phase I clinical trials in patients with solid cancers. However, neither the exact mechanisms of action of AGM-1470 nor its effects on the host of normal cells have been extensively studied. Recently, we showed that AGM-1470 enhanced the proliferation of B lymphocytes in the presence of T cells. Since AGM-1470 could potentially be used in patients with lymphoma, it was urgent to test the effect of the molecule on the proliferation of tumor lymphocytes. Methods The possible effect of AGM-1470 on the proliferation of normal or tumor lymphocytes was evaluated by thymidine-incorporation assays. Normal T and B lymphocytes were purified from human tonsils. The tumor lymphocytes used in the study were Molt 3, Molt 4 and Jurkatt cell lines for the T lineage and Daudi and Radji cell lines for the B lineage. Results As shown previously, AGM-1470 stimulates the proliferation of normal B lymphocytes through an action on normal T cells. The angioinhibin was ineffective on the proliferation of both T and B transformed cells. Moreover, in the presence of the drug, tumor T cells co-cultured with normal B lymphocytes did not induce any increase in B cell proliferation, as previously observed with normal T lymphocytes. Inversely, tumor B cells co-cultured with normal T lymphocytes were insensitive to the drug. Conclusions Our results demonstrate that AGM-1470 is ineffective on lymphoid tumor cell proliferation and could potentially be safely administered to lymphoma patients. |
Databáze: | OpenAIRE |
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