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Clin Oncol (R Coll Radiol). 2014 May;26(5):277-88. doi: 10.1016/j.clon.2014.02.002. Epub 2014 Mar 3.

The meaning, measurement and modification of hypoxia in the laboratory and the clinic.

Author information

1
The Gray Institute for Radiation Oncology and Biology, Department of Oncology, University of Oxford, Oxford, UK.
2
Wolfson Molecular Imaging Centre, Manchester, UK.
3
Centre for Imaging Sciences, Institute of Population Health, Manchester, UK.
4
Manchester Pharmacy School, Cambridge-Manchester Cancer Research UK Comprehensive Imaging Centre, Manchester Academic Health Sciences Centre, The University Manchester, Manchester, UK. Electronic address: kaye.williams@manchester.ac.uk.

Abstract

Hypoxia was identified as a microenvironmental component of solid tumours over 60 years ago and was immediately recognised as a potential barrier to therapy through the reliance of radiotherapy on oxygen to elicit maximal cytotoxicity. Over the last two decades both clinical and experimental studies have markedly enhanced our understanding of how hypoxia influences cellular behaviour and therapy response. Furthermore, they have confirmed early assumptions that low oxygenation status in tumours is an exploitable target in cancer therapy. Generally such approaches will be more beneficial to patients with hypoxic tumours, necessitating the use of biomarkers that reflect oxygenation status. Tissue biomarkers have shown utility in many studies. Further significant advances have been made in the non-invasive measurement of tumour hypoxia with positron emission tomography, magnetic resonance imaging and other imaging modalities. Here, we describe the complexities of defining and measuring tumour hypoxia and highlight the therapeutic approaches to combat it.

KEYWORDS:

Hypoxia; hypoxia-activated prodrugs; imaging; oxygen; radiation

PMID:
24602562
DOI:
10.1016/j.clon.2014.02.002
[Indexed for MEDLINE]
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