Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1987 Oct;56(4):383-8.
doi: 10.1038/bjc.1987.211.

Stromal sensitivity to radiation and hyperthermia

Affiliations
Free PMC article

Stromal sensitivity to radiation and hyperthermia

S A Hill et al. Br J Cancer. 1987 Oct.
Free PMC article

Abstract

The influence on stroma of heat alone, X-rays alone or the combined treatment, has been studied using the tumour bed effect (TBE) as an assay. Ca NT cells have been implanted into previously treated subcutaneous sites as an angiogenic stimulus. The vascular damage is then assessed by the reduced tumour growth rate, which results from inadequate vascular proliferation. A range of X-ray doses was used and large alterations in latent period for growth to 2 mm diameter were followed by smaller alterations in the growth rate of established tumours. A dose response relationship was seen for latency (0-20 Gy) and for growth rate (0-16 Gy). A range of subcutaneous temperatures was obtained by immersion in a water bath for 60 minutes at 40 degrees, 41.5 degrees, 43 degrees or 44.5 degrees C. A slight retardation of tumour growth was seen after 41.5 degrees C, but an unexpected acceleration resulted from the highest heat treatment. Combined heat and X-ray treatments showed thermal sensitization of the X-ray induced TBE at 41.5 degrees C, with a reversal at higher temperatures. At 43 degrees C and 44.5 degrees C a mild thermal burn was induced and this appeared to elicit neovascularisation that could be utilized by the implanted tumour cells. Delayed implantation of tumour cells (at 4 weeks instead of 1 day) abolished this effect.

PubMed Disclaimer

References

    1. Br J Cancer. 1980 Feb;41(2):309-12 - PubMed
    1. Cancer Res. 1986 Jan;46(1):355-61 - PubMed
    1. Br J Cancer. 1967 Mar;21(1):108-23 - PubMed
    1. Br J Cancer. 1974 Sep;30(3):246-60 - PubMed
    1. Int J Radiat Oncol Biol Phys. 1985 Mar;11(3):547-53 - PubMed

Publication types