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Cited by 384

The DOI matches its Crossref record; 124 of the 124 references it cites were found in a registry or an index.

Receptor tyrosine kinase signalling as a target for cancer intervention strategies.

Open access
Zwick, E, Bange, J, Ullrich, A·2001·Endocrine-related cancer

Abstract

In multicellular organisms, communication between individual cells is essential for the regulation and coordination of complex cellular processes such as growth, differentiation, migration and apoptosis. The plethora of signal transduction networks mediating these biological processes is regulated in part by polypeptide growth factors that can generate signals by activating cell surface receptors either in paracrine or autocrine manner. The primary mediators of such physiological cell responses are receptor tyrosine kinases (RTKs) that couple ligand binding to downstream signalling cascades and gene transcription. Investigations over the past 18 years have revealed that RTKs are not only key regulators of normal cellular processes but are also critically involved in the development and progression of human cancers. Therefore, signalling pathways controlled by tyrosine kinases offer unique opportunities for pharmaco logical intervention. The aim of this review is to give a broad overview of RTK signalling involved in tumorigenesis and the possibility of target-selective intervention for anti-cancer therapy.

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Metadata

Authors
Zwick, E., Bange, J., & Ullrich, A.
Venue
Endocrine-related cancer
Published
2001-09
Volume
8
Issue
3
Pages
161-173
ISSN
1351-0088 (ISSN-L)
OpenAlex
W2142776762
Cited by
384
References
124
FWCI
4.21
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Receptor tyrosine kinase signalling as a target for cancer intervention strategies. https://app.cochat.ai/papers/10.1677/erc.0.0080161
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Zwick, E., Bange, J., & Ullrich, A. (2001). Receptor tyrosine kinase signalling as a target for cancer intervention strategies. Endocrine-related cancer. https://doi.org/10.1677/erc.0.0080161

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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.