Radiation induces aerobic glycolysis through reactive oxygen species
Creators
- 1. School of Medicine, Duke University, Durham (United States)
- 2. Biomedical Engineering Department, Duke University, Durham (United States)
- 3. Radiation Oncology Department, Duke University, Durham (United States)
Description
Background and purpose: Although radiation induced reoxygenation has been thought to increase radiosensitivity, we have shown that its associated oxidative stress can have radioprotective effects, including stabilization of the transcription factor hypoxia inducible factor 1 (HIF-1). HIF-1 is known to regulate many of the glycolytic enzymes, thereby promoting aerobic glycolysis, which is known to promote treatment resistance. Thus, we hypothesized that reoxygenation after radiation would increase glycolysis. We previously showed that blockade of oxidative stress using a superoxide dismutase (SOD) mimic during reoxygenation can downregulate HIF-1 activity. Here we tested whether concurrent use of this drug with radiotherapy would reduce the switch to a glycolytic phenotype. Materials and methods: 40 mice with skin fold window chambers implanted with 4T1 mammary carcinomas were randomized into (1) no treatment, (2) radiation alone, (3) SOD mimic alone, and (4) SOD mimic with concurrent radiation. All mice were imaged on the ninth day following tumor implantation (30 h following radiation treatment) following injection of a fluorescent glucose analog, 2-[N-(7-nitrobenz-2-oxa-1,3-diaxol-4-yl)amino]-2-deoxyglucose (2-NBDG). Hemoglobin saturation was measured by using hyperspectral imaging to quantify oxygenation state. Results: Mice treated with radiation showed significantly higher 2-NBDG fluorescence compared to controls (p = 0.007). Hemoglobin saturation analysis demonstrated reoxygenation following radiation, coinciding with the observed increase in glycolysis. The concurrent use of the SOD mimic with radiation demonstrated a significant reduction in 2-NBDG fluorescence compared to effects seen after radiation alone, while having no effect on reoxygenation. Conclusions: Radiation induces an increase in tumor glucose demand approximately 30 h following therapy during reoxygenation. The use of an SOD mimic can prevent the increase in aerobic glycolysis when used concurrently with radiation, without preventing reoxygenation
Availability note (English)
Available from http://dx.doi.org/10.1016/j.radonc.2013.02.013Additional details
Identifiers
- DOI
- 10.1016/j.radonc.2013.02.013;
- PII
- S0167-8140(13)00065-0;
Publishing Information
- Journal Title
- Radiotherapy and Oncology
- Journal Volume
- 106
- Journal Issue
- 3
- Journal Page Range
- p. 390-396
- ISSN
- 0167-8140
- CODEN
- RAONDT
INIS
- Country of Publication
- Ireland
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45079670
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CARCINOMAS; FLUORESCENCE; GLUCOSE; GLYCOLYSIS; HEMOGLOBIN; MICE; OXIDATION; PHENOTYPE; RADIOSENSITIVITY; RADIOTHERAPY; SUPEROXIDE DISMUTASE; TRANSCRIPTION FACTORS
- Descriptors DEC
- ALDEHYDES; ANIMALS; CARBOHYDRATES; CARBOXYLIC ACIDS; CHEMICAL REACTIONS; DECOMPOSITION; DISEASES; EMISSION; ENZYMES; GLOBINS; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; HEXOSES; LUMINESCENCE; MAMMALS; MEDICINE; METABOLISM; MONOSACCHARIDES; NEOPLASMS; NUCLEAR MEDICINE; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; OXIDOREDUCTASES; PHOTON EMISSION; PIGMENTS; PORPHYRINS; PROTEINS; RADIOLOGY; RODENTS; SACCHARIDES; SENSITIVITY; THERAPY; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.