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Cited by 359

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Inhibition of tumor angiogenesis mediated by cartilage.

Open access
Brem, H, Folkman, J·1975·The Journal of experimental medicine

Abstract

Capillary proliferation induced by tumor is shown to be inhibited by neonatal scapular cartilage. Using the rabbit cornea as an assay, the cartilage implant decreased the rate of capillary growth, induced by tumor, by an average of 75%. Vascularization was prevented completely in 28% of tumors. The inhibitory effect of small cartilage implants operates over distances of up to 2.0 mm and displays a gradient from the cartilage source. The experiments suggest that the cartilage inhibitor does not antagonize tumor angiogenesis factor, but appears to inhibit capillary proliferation directly. The inhibitory material does not elicit an inflammatory response in either the rabbit cornea or in the chick chorioallantoic membrane. Thus with further purification, it may prove useful as a means of maintining tumor dormancy by "antiangiogenesis."

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Crossref · 10.1084/jem.141.2.427

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Metadata

Authors
Brem, H., & Folkman, J.
Venue
The Journal of experimental medicine
Published
1975-02-01
Volume
141
Issue
2
Pages
427-439
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W1997107937
Cited by
359
References
1
FWCI
6.63
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Inhibition of tumor angiogenesis mediated by cartilage. https://app.cochat.ai/papers/10.1084/jem.141.2.427
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Brem, H., & Folkman, J. (1975). Inhibition of tumor angiogenesis mediated by cartilage. The Journal of experimental medicine. https://doi.org/10.1084/jem.141.2.427

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.