Cited by 340Proteoglycans and glycosaminoglycans researchProtease and Inhibitor MechanismsMechanisms of cancer metastasis

Heparanase, Hyaluronan, and CD44 in Cancers: A Breast Carcinoma Perspective

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Götte, Martin, Yip, George W.·2006·Cancer Research

Abstract

Glycosaminoglycans are major constituents of the cancer cell surface and the tumor stroma. The heparan sulfate degrading enzyme heparanase, hyaluronan, and its receptor CD44 are up-regulated in breast cancer, generating a microenvironment that promotes tumor progression and metastasis. Recent experimental and clinical evidence shows that heparanase, hyaluronan, and CD44 regulate cancer cell proliferation, migration, and invasion, as well as tumor-associated angiogenesis and are correlated with patient survival. These findings suggest that they may be used as prognostic factors and targets for breast cancer treatment. (Cancer Res 2006; 66(21): 10233-7)

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Crossref · 10.1158/0008-5472.can-06-1464

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Research works printed but not linked: 2

  1. Watabe T, Yoshida K, Shindoh M, et al. The Ets-1 and Ets-2 transcription factors activate the promoters for invasion-associated urokinase and collagenase genes in response to epidermal growth factor. Int J Cancer 1998; 77:128-37.
  2. Zeng C, Toole BP, Kinney SD, Kuo JW, Stamenkovic I. Inhibition of tumor growth in vivo by hyaluronan oligomers. Int J Cancer 1998;77:396-401.

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Authors
Götte, M., & Yip, G. W.
Affiliations
  • 1Department of Obstetrics and Gynecology, Münster University Hospital, Münster, Germany and
  • National University of Singapore (SG)
Venue
Cancer Research
Published
2006-11-01
Volume
66
Issue
21
Pages
10233-10237
ISSN
  • 0008-5472 (ISSN-L)
  • 1538-7445
OpenAlex
W2134709252
Cited by
340
References
58
Citations by year
2026: 3 · 2025: 7 · 2024: 6 · 2023: 11 · 2022: 12 · 2021: 20 · 2020: 14 · 2019: 9 · 2018: 16 · 2017: 22 · 2016: 22 · 2015: 19 · 2014: 25 · 2013: 28 · 2012: 24
FWCI
1.57
Type
journal article
Language
en
Open access
Locations
  • Cancer Research (publishedVersion)
  • PubMed (publishedVersion)
  • National University of Singapore (submittedVersion)
Funders
  • Deutsche Forschungsgemeinschaft
  • Medical Research Council
  • National Medical Research Council
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Protease and Inhibitor Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mechanisms of cancer metastasis
Keywords
heparanase, hyaluronic acid, CD44, breast cancer, glycosaminoglycans, tumor microenvironment, tumor stroma, metastasis, tumor progression, angiogenesis, tumor cell proliferation, cell migration and invasion, prognostic factors, therapeutic target
MeSH terms
Heparanase, Breast Neoplasms, Female, Glucuronidase, Humans, Hyaluronic Acid, Neoplasm Invasiveness, Hyaluronan Receptors, Cell Proliferation

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