Heparin-binding epidermal growth factor-like growth factor as a novel targeting molecule for cancer therapy

Shingo Miyamoto, Hiroshi Yagi, Fusanori Yotsumoto, Tatsuhiko Kawarabayashi, Eisuke Mekada

研究成果: Contribution to journalReview article査読

107 被引用数 (Scopus)

抄録

HB-EGF, a member of the EGF family of growth factors, exerts its biological activity through activation of the EGFR and other ErbB receptors. HB-EGF participates in diverse biological processes, including heart development and maintenance, skin wound healing, eyelid formation, blastocyst implantation, progression of atherosclerosis and tumor formation, through the activation of signaling molecules downstream of ErbB receptors and interactions with molecules associated with HB-EGF. Recent studies have indicated that HB-EGF gene expression is significantly elevated in many human cancers and its expression level in a number of cancer-derived cell lines is much higher than those of other EGFR ligands. Several lines of evidence have indicated that HB-EGF plays a key role in the acquisition of malignant phenotypes, such as tumorigenicity, invasion, metastasis and resistance to chemotherapy. Studies in vitro and in vivo have indicated that HB-EGF expression is essential for tumor formation of cancer-derived cell lines. CRM197, a specific inhibitor of HB-EGF, and an antibody against HB-EGF are both able to inhibit tumor growth in nude mice. These results indicate that HB-EGF is a promising target for cancer therapy, and that the development of targeting tools against HB-EGF could represent a novel type of therapeutic strategy, as an alternative to targeting ErbB receptors.

本文言語英語
ページ(範囲)341-347
ページ数7
ジャーナルCancer Science
97
5
DOI
出版ステータス出版済み - 5 2006

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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