Fatigue is one of the most prevalent symptoms that has the largest detrimental influence on quality of life in cancer patients, but it is also one of the least understood. The purpose of this study was to examine into changes in mitochondrial function and cancer-related fatigue in patients who were getting localised radiation therapy for non-metastatic prostate cancer (XRT).
We suggested a
mitochondrial bioenergetic mechanism of radiation-induced fatigue that links
defective oxidative phosphorylation (OXPHOS) via a complex III defect and ATP
depletion as a result of XRT. In prostate cancer patients' peripheral blood
mononuclear cells (PBMCs), integrated mitochondrial function was assessed as
mitochondrial OXPHOS. The improved Piper Fatigue Scale was used to assess
fatigue. Before (day 0) and after (day 21) XRT, data was collected.
At day 21 of XRT,
fatigue symptoms worsened in 15 individuals with prostate cancer (p 0.05). At
day 21, the rates of mitochondrial OXPHOS complex III-linked and uncoupled
complex III in PBMCs were significantly lower than before XRT (p 0.05).
Furthermore, a higher fatigue score was linked to a reduced OXPHOS complex
III-linked respiration rate in people who had XRT.
Author(S) Details
Chao-Pin Hsiao
The Frances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, OH, USA.
Mei-Kuang Chen
Department of Psychology, University of Arizona, Tucson, AZ, USA.
Barbara Daly
The Frances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, OH, USA.
Charles Hoppel
Center for Mitochondrial Disease, Department of Pharmacology, School of Medicine, Case Western Reserve University, Cleveland, OH, USA.
View Book:- https://stm.bookpi.org/IDMMR-V3/article/view/5471
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