TY - JOUR
T1 - Angiogenesis Inhibition by Minocycline
AU - Tamargo, Rafael J.
AU - Bok, Robert A.
AU - Brenr, Henry
N1 - Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 1991/1
Y1 - 1991/1
N2 - We describe a new inhibitor of angiogenesis, minocycline, a semisynthetic tetracycline antimicrobial with anticollagenase properties. Mino cycline was incorporated into controlled release polymers and tested inthe rabbit cornea against neovascularization in the presence of the VX2 mcarcinoma. Inhibition by minocycline was shown to be comparable to that of the combination of heparin and cortisone, a potent inhibitor of angio genesis. Minocycline decreased tumor-induced angiogenesis by a factor of 4.5, 4.4, and 2.9 at 7, 14, and 21 days, respectively. At the end of the experiment, whereas the corneas with empty polymers had large, inva sive, exophytic tumors, none of the corneas with minocycline had such vascular masses. Recently, studies of agents that disrupt collagen synthe sis and deposition have yielded several new angiogenesis inhibitors. We suggest that investigation of agents that disrupt collagenolysis may similarly identify other angiogenesis inhibitors and further clarify the mechanisms of angiogenesis.
AB - We describe a new inhibitor of angiogenesis, minocycline, a semisynthetic tetracycline antimicrobial with anticollagenase properties. Mino cycline was incorporated into controlled release polymers and tested inthe rabbit cornea against neovascularization in the presence of the VX2 mcarcinoma. Inhibition by minocycline was shown to be comparable to that of the combination of heparin and cortisone, a potent inhibitor of angio genesis. Minocycline decreased tumor-induced angiogenesis by a factor of 4.5, 4.4, and 2.9 at 7, 14, and 21 days, respectively. At the end of the experiment, whereas the corneas with empty polymers had large, inva sive, exophytic tumors, none of the corneas with minocycline had such vascular masses. Recently, studies of agents that disrupt collagen synthe sis and deposition have yielded several new angiogenesis inhibitors. We suggest that investigation of agents that disrupt collagenolysis may similarly identify other angiogenesis inhibitors and further clarify the mechanisms of angiogenesis.
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M3 - Article
C2 - 1702361
AN - SCOPUS:0025924722
SN - 0008-5472
VL - 51
SP - 672
EP - 675
JO - Cancer Research
JF - Cancer Research
IS - 2
ER -