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Cited by 264

The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.

Controlling escape from angiogenesis inhibitors

Open access
Sennino, Barbara, McDonald, Donald M.·2012·Nature Reviews Cancer

Abstract

Selective inhibition of vascular endothelial growth factor (VEGF) increases the efficacy of chemotherapy and has beneficial effects on multiple advanced cancers, but response is often limited and the disease eventually progresses. Changes in the tumour microenvironment — hypoxia among them — that result from vascular pruning, suppressed angiogenesis and other consequences of VEGF inhibition can promote escape and tumour progression. New therapeutic approaches that target pathways that are involved in the escape mechanisms add the benefits of blocking tumour progression to those of slowing tumour growth by inhibiting angiogenesis.

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Crossref · 10.1038/nrc3366

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Metadata

Authors
Sennino, B., & McDonald, D. M.
Venue
Nature Reviews Cancer
Published
2012-09-24
Volume
12
Issue
10
Pages
699-709
ISSN
  • 1474-175X (ISSN-L)
  • 1474-1768
OpenAlex
W1978148288
Cited by
264
References
29
FWCI
1.65
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Controlling escape from angiogenesis inhibitors. https://app.cochat.ai/papers/10.1038/nrc3366
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Sennino, B., & McDonald, D. M. (2012). Controlling escape from angiogenesis inhibitors. Nature Reviews Cancer. https://doi.org/10.1038/nrc3366

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.