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PMID: 7505321 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The combination of antiangiogenic agents to inhibit primary tumor growth and metastasis.

Journal of pediatric surgery ·Vol. 28 ·No. 10 ·1993-10-00 ·Pages 1253-7

Brem H, Gresser I, Grosfeld J, Folkman J

Abstract

Neovascularization is a critical component for the growth of tumors and is a dominant feature in diseases such as diabetic retinopathy and hemangiomas in infancy. Angiogenesis inhibition is a potentially important therapeutic modality. We have previously reported that AGM-1470 is a fungal-derived angiogenesis inhibitor that suppresses primary tumor growth and metastases and is also nontoxic. alpha-Interferon, an angiogenesis inhibitor, is effective in the treatment of life-threatening hemangiomas. We therefore attempted to treat murine primary tumors and metastases with a combination of AGM-1470 and alpha/beta-interferon. Treatment began after solid tumors formed. Six-week-old syngeneic C57BI/6 mice were treated for 21 days with either AGM-1470, or alpha/beta-interferon or AGM-1470 + alpha/beta-interferon. The combination of the angiogenesis inhibitors AGM-1470 and alpha/beta-interferon suppressed tumor growth by 80% compared with controls (P < or = .001). AGM-1470 and alpha/beta-interferon inhibited pulmonary metastatic tumor growth greater than sevenfold (P < or = .001) compared with controls. These effects were better than either inhibitor alone, and the combined effect was additive. Combination of angiogenesis inhibitors may be useful in the treatment of tumors and other angiogenesis-dependent diseases.

MeSH Terms
Animals Antibiotics, Antineoplastic/administration & dosage Antineoplastic Combined Chemotherapy Protocols/therapeutic use Carcinoma/blood supply,drug therapy,pathology,secondary Cyclohexanes Drug Screening Assays, Antitumor Drug Synergism Interferon-alpha/administration & dosage Interferon-beta/administration & dosage Lung/drug effects,pathology Lung Neoplasms/blood supply,drug therapy,pathology,secondary Male Mice Mice, Inbred C57BL Neoplasm Transplantation Neovascularization, Pathologic/drug therapy,pathology O-(Chloroacetylcarbamoyl)fumagillol Sesquiterpenes/administration & dosage Time Factors
Chemicals
Antibiotics, Antineoplastic Cyclohexanes Interferon-alpha Sesquiterpenes Interferon-beta O-(Chloroacetylcarbamoyl)fumagillol
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Brem H
Department of Surgery, Children's Hospital, Boston, MA 02115.
Gresser I
Grosfeld J
Folkman J
Article Info
Journal
Journal of pediatric surgery
Abbr.
J Pediatr Surg
ISSN
0022-3468
Published
1993-10-00
Pages
1253-7
Language
English
Region
United States
NLM ID
0052631
Subset
IM
Grants
NCI NIH HHS · CA-37395-08 · United States
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