Literature DB >> 414306

Tumor cell respiration following irradiation.

J J Clement, C W Song, T T Sand.   

Abstract

Oxygen consumption rates for mouse mastocytoma cells examined from 3 to 4 hours after x-irradiation with 250-2000 rads were consistently higher than controls. Cyclic fluctuations in oxygen consumption per cell were dose-dependent; peaks in consumption were generally greater in magnitude and occurred later in time with increasing dose. The cyclic response in consumption is probably due to cell synchronization effects, while the overall higher respiration rates of irradiated cells may reflect increased metabolic activity in response to radiation damage. Oxygen consumption rates for the total cell population were cyclic after 250 and 500 rads, but declined steadily after 1000 or 2000 rads; oxygen consumption rates tended to be lower than controls, especially 12-24 hours postirradiation. Differences between cellular and population oxygen consumption rates reflect changes in cell number after irradiation. It is suggested that postirradiation reoxygenation kinetics in solid tumors may result from changes in tumor oxygen demand.

Entities:  

Mesh:

Year:  1978        PMID: 414306     DOI: 10.1148/126.2.507

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


  1 in total

1.  Endothelial cell death after ionizing radiation does not impair vascular structure in mouse tumor models.

Authors:  Ruth J Muschel; Bostjan Markelc; Jakob R Kaeppler; Jianzhou Chen; Mario Buono; Jenny Vermeer; Pavitra Kannan; Wei-Chen Cheng; Dimitrios Voukantsis; James M Thompson; Mark A Hill; Danny Allen; Ana Gomes; Veerle Kersemans; Paul Kinchesh; Sean Smart; Francesca Buffa; Claus Nerlov
Journal:  EMBO Rep       Date:  2022-07-18       Impact factor: 9.071

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.