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Exploring the role of endothelium in the tumour response to anti-angiogenic therapy. | LitMetric

Exploring the role of endothelium in the tumour response to anti-angiogenic therapy.

Biochem Soc Trans

*Tumour Angiogenesis Program, Peter MacCallum Cancer Centre, East Melbourne, Victoria 3002, Australia.

Published: December 2014

AI Article Synopsis

  • Cancer often grows because of increased blood vessel formation, which helps tumors get bigger and spread.
  • Doctors have tried to stop this blood vessel growth with special medicines, but they don’t always work for everyone.
  • Researchers are studying how these blood vessels inside tumors respond to treatment to find better ways to help patients with cancer.

Article Abstract

A chronic hyperactivated angiogenic state in cancer plays an important role in tumour growth and metastasis and has been identified as one of the hallmarks of cancer. Inhibition of this process has been associated with tumour suppression in many pre-clinical contexts using different animal tumour models. Anti-angiogenic therapeutics were subsequently developed and used to treat several prevalent types of human cancer. However, recent clinical experience has revealed limitations of this approach in treating cancer as patient response varies over a wide range. Given that there are complex underlying molecular and cellular changes provoked by anti-angiogenic treatment within the tumour microenvironment (TME), it is not surprising that modest effectiveness and resistance have been observed in the clinical setting. This article discusses these issues in the context of VEGF-A-targeted anti-angiogenic treatment of cancer and provides insight into the importance of tumour endothelium for understanding the tumour response to anti-angiogenic therapy. Special consideration is also given to possible approaches for investigating how endothelium contributes to the tumour response to anti-angiogenic agents and for exploring the therapeutic and biomarker potential of targeting tumour endothelium.

Download full-text PDF

Source
http://dx.doi.org/10.1042/BST20140173DOI Listing

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