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Cited by 358

The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.

Distinct Antitumor Properties of a Type IV Collagen Domain Derived from Basement Membrane

Open access
Maeshima, Yohei, Colorado, Pablo C., Torre, Adriana, Holthaus, Kathryn A., Grunkemeyer, James A., Ericksen, Mark B., Hopfer, Helmut, Xiao, Yingwen, Stillman, Isaac E., Kalluri, Raghu·2000·Journal of Biological Chemistry

Abstract

Vascular basement membrane is an important structural component of blood vessels. During angiogenesis this membrane undergoes many alterations and these changes are speculated to influence the formation of new capillaries. Type IV collagen is a major component of vascular basement membrane, and recently we identified a fragment of type IV collagen alpha2 chain with specific anti-angiogenic properties (Kamphaus, G. D., Colorado, P. C., Panka, D. J., Hopfer, H., Ramchandran, R., Torre, A., Maeshima, Y., Mier, J. W., Sukhatme, V. P., and Kalluri, R. (2000) J. Biol. Chem. 275, 1209-1215). In the present study we characterize two different antitumor activities associated with the noncollagenous 1 (NC1) domain of the alpha3 chain of type IV collagen. This domain was previously discovered to possess a C-terminal peptide sequence (amino acids 185-203) that inhibits melanoma cell proliferation (Han, J., Ohno, N., Pasco, S., Monboisse, J. C., Borel, J. P., and Kefalides, N. A. (1997) J. Biol. Chem. 272, 20395-20401). In the present study, we identify the anti-angiogenic capacity of this domain using several in vitro and in vivo assays. The alpha3(IV)NC1 inhibited in vivo neovascularization in matrigel plug assays and suppressed tumor growth of human renal cell carcinoma (786-O) and prostate carcinoma (PC-3) in mouse xenograft models associated with in vivo endothelial cell-specific apoptosis. The anti-angiogenic activity was localized to amino acids 54-132 using deletion mutagenesis. This anti-angiogenic region is separate from the 185-203 amino acid region responsible for the antitumor cell activity. Additionally, our experiments indicate that the antitumor cell activity is not realized until the peptide region is exposed by truncation of the alpha3(IV)NC1 domain, a requirement not essential for the anti-angiogenic activity of this domain. Collectively, these results effectively highlight the distinct and unique antitumor properties of the alpha3(IV)NC1 domain and the potential use of this molecule for inhibition of tumor growth.

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Metadata

Authors
Maeshima, Y., Colorado, P. C., Torre, A., Holthaus, K. A., Grunkemeyer, J. A., Ericksen, M. B., Hopfer, H., Xiao, Y., Stillman, I. E., & Kalluri, R.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
2000-07
Volume
275
Issue
28
Pages
21340-21348
ISSN
0021-9258 (ISSN-L)
OpenAlex
W2014696732
Cited by
358
References
47
FWCI
5.41
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Distinct Antitumor Properties of a Type IV Collagen Domain Derived from Basement Membrane. https://app.cochat.ai/papers/10.1074/jbc.m001956200
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Maeshima, Y., Colorado, P. C., Torre, A., Holthaus, K. A., Grunkemeyer, J. A., Ericksen, M. B., Hopfer, H., Xiao, Y., Stillman, I. E., & Kalluri, R. (2000). Distinct Antitumor Properties of a Type IV Collagen Domain Derived from Basement Membrane. Journal of Biological Chemistry. https://doi.org/10.1074/jbc.m001956200

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