Proteomic Serum Profile of Fatigued Men Receiving Localized External Beam Radiation Therapy for Non-Metastatic Prostate Cancer

Fatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown. This study describes proteome changes from sera of fatigued men with non-metastatic prostate cancer receiving external beam radiation therapy (EBRT). Fatigue scores, measured by the Functional...

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Published inJournal of pain and symptom management Vol. 47; no. 4; pp. 748 - 756.e4
Main Authors Lukkahatai, Nada, Patel, Sajni, Gucek, Marjan, Hsiao, Chao-Pin, Saligan, Leorey N.
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.04.2014
Elsevier
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Online AccessGet full text
ISSN0885-3924
1873-6513
1873-6513
DOI10.1016/j.jpainsymman.2013.05.016

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Abstract Fatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown. This study describes proteome changes from sera of fatigued men with non-metastatic prostate cancer receiving external beam radiation therapy (EBRT). Fatigue scores, measured by the Functional Assessment of Chronic Illness Therapy-Fatigue, and serum were collected from 12 subjects at baseline (before EBRT) and at midpoint (Day 21) of EBRT. Depleted sera from both time points were analyzed using two-dimensional difference gel electrophoresis, and up/down regulated proteins were identified using liquid chromatography-tandem mass spectrometry. Western blot analyses confirmed the protein changes observed. Results showed that apolipoprotein (Apo)A1, ApoE, and transthyretin (TTR) consistently changed from baseline (Day 0) to midpoint (Day 21). The mean ApoE level of subjects with high change in fatigue (HF: n = 9) increased significantly from baseline to midpoint and were higher than in subjects with no change in fatigue. The mean ApoA1 level was higher in HF subjects at baseline and at midpoint than in no fatigue subjects at both time points. The mean TTR level of no fatigue subjects was higher at baseline and midpoint than in HF subjects. These ApoE, ApoA1, and TTR results may assist in understanding pathways that can explain fatigue progression etiology in this clinical population.
AbstractList Fatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown.CONTEXTFatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown.This study describes proteome changes from sera of fatigued men with non-metastatic prostate cancer receiving external beam radiation therapy (EBRT).OBJECTIVESThis study describes proteome changes from sera of fatigued men with non-metastatic prostate cancer receiving external beam radiation therapy (EBRT).Fatigue scores, measured by the Functional Assessment of Chronic Illness Therapy-Fatigue, and serum were collected from 12 subjects at baseline (before EBRT) and at midpoint (Day 21) of EBRT. Depleted sera from both time points were analyzed using two-dimensional difference gel electrophoresis, and up/down regulated proteins were identified using liquid chromatography-tandem mass spectrometry. Western blot analyses confirmed the protein changes observed.METHODSFatigue scores, measured by the Functional Assessment of Chronic Illness Therapy-Fatigue, and serum were collected from 12 subjects at baseline (before EBRT) and at midpoint (Day 21) of EBRT. Depleted sera from both time points were analyzed using two-dimensional difference gel electrophoresis, and up/down regulated proteins were identified using liquid chromatography-tandem mass spectrometry. Western blot analyses confirmed the protein changes observed.Results showed that apolipoprotein (Apo)A1, ApoE, and transthyretin (TTR) consistently changed from baseline (Day 0) to midpoint (Day 21). The mean ApoE level of subjects with high change in fatigue (HF: n = 9) increased significantly from baseline to midpoint and were higher than in subjects with no change in fatigue. The mean ApoA1 level was higher in HF subjects at baseline and at midpoint than in no fatigue subjects at both time points. The mean TTR level of no fatigue subjects was higher at baseline and midpoint than in HF subjects.RESULTSResults showed that apolipoprotein (Apo)A1, ApoE, and transthyretin (TTR) consistently changed from baseline (Day 0) to midpoint (Day 21). The mean ApoE level of subjects with high change in fatigue (HF: n = 9) increased significantly from baseline to midpoint and were higher than in subjects with no change in fatigue. The mean ApoA1 level was higher in HF subjects at baseline and at midpoint than in no fatigue subjects at both time points. The mean TTR level of no fatigue subjects was higher at baseline and midpoint than in HF subjects.These ApoE, ApoA1, and TTR results may assist in understanding pathways that can explain fatigue progression etiology in this clinical population.CONCLUSIONThese ApoE, ApoA1, and TTR results may assist in understanding pathways that can explain fatigue progression etiology in this clinical population.
AbstractContextFatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown. ObjectivesThis study describes proteome changes from sera of fatigued men with non-metastatic prostate cancer receiving external beam radiation therapy (EBRT). MethodsFatigue scores, measured by the Functional Assessment of Chronic Illness Therapy-Fatigue, and serum were collected from 12 subjects at baseline (before EBRT) and at midpoint (Day 21) of EBRT. Depleted sera from both time points were analyzed using two-dimensional difference gel electrophoresis, and up/down regulated proteins were identified using liquid chromatography-tandem mass spectrometry. Western blot analyses confirmed the protein changes observed. ResultsResults showed that apolipoprotein (Apo)A1, ApoE, and transthyretin (TTR) consistently changed from baseline (Day 0) to midpoint (Day 21). The mean ApoE level of subjects with high change in fatigue (HF: n = 9) increased significantly from baseline to midpoint and were higher than in subjects with no change in fatigue. The mean ApoA1 level was higher in HF subjects at baseline and at midpoint than in no fatigue subjects at both time points. The mean TTR level of no fatigue subjects was higher at baseline and midpoint than in HF subjects. ConclusionThese ApoE, ApoA1, and TTR results may assist in understanding pathways that can explain fatigue progression etiology in this clinical population.
Fatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown. This study describes proteome changes from sera of fatigued men with non-metastatic prostate cancer receiving external beam radiation therapy (EBRT). Fatigue scores, measured by the Functional Assessment of Chronic Illness Therapy-Fatigue, and serum were collected from 12 subjects at baseline (before EBRT) and at midpoint (Day 21) of EBRT. Depleted sera from both time points were analyzed using two-dimensional difference gel electrophoresis, and up/down regulated proteins were identified using liquid chromatography-tandem mass spectrometry. Western blot analyses confirmed the protein changes observed. Results showed that apolipoprotein (Apo)A1, ApoE, and transthyretin (TTR) consistently changed from baseline (Day 0) to midpoint (Day 21). The mean ApoE level of subjects with high change in fatigue (HF: n = 9) increased significantly from baseline to midpoint and were higher than in subjects with no change in fatigue. The mean ApoA1 level was higher in HF subjects at baseline and at midpoint than in no fatigue subjects at both time points. The mean TTR level of no fatigue subjects was higher at baseline and midpoint than in HF subjects. These ApoE, ApoA1, and TTR results may assist in understanding pathways that can explain fatigue progression etiology in this clinical population.
Context Fatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown. Objectives This study describes proteome changes from sera of fatigued men with non-metastatic prostate cancer receiving external beam radiation therapy (EBRT). Methods: Fatigue scores, measured by the Functional Assessment of Chronic Illness Therapy-Fatigue, and serum were collected from 12 subjects at baseline (before EBRT) and at midpoint (Day 21) of EBRT. Depleted sera from both time points were analyzed using two-dimensional difference gel electrophoresis, and up/down regulated proteins were identified using liquid chromatography-tandem mass spectrometry. Western blot analyses confirmed the protein changes observed. Results: Results showed that apolipoprotein (Apo)A1, ApoE, and transthyretin (TTR) consistently changed from baseline (Day 0) to midpoint (Day 21). The mean ApoE level of subjects with high change in fatigue (HF: n = 9) increased significantly from baseline to midpoint and were higher than in subjects with no change in fatigue. The mean ApoA1 level was higher in HF subjects at baseline and at midpoint than in no fatigue subjects at both time points. The mean TTR level of no fatigue subjects was higher at baseline and midpoint than in HF subjects. Conclusion: These ApoE, ApoA1, and TTR results may assist in understanding pathways that can explain fatigue progression etiology in this clinical population. [Copyright U.S. Cancer Pain Relief Committee. Published by Elsevier Inc.]
Author Gucek, Marjan
Hsiao, Chao-Pin
Patel, Sajni
Saligan, Leorey N.
Lukkahatai, Nada
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Issue 4
Keywords Western blot
External beam radiation therapy
fatigue
prostate cancer
quantitative proteomics
Human
Urinary system disease
Prostate disease
Fatigue
Male
Early stage
Malignant tumor
Extracorporeal irradiation
Proteomics
Immunoblotting assay
Adult
Serum
Male genital diseases
Prostate cancer
Localized
Cancer
Quantitative analysis
Language English
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CC BY 4.0
Published by Elsevier Inc.
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Snippet Fatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown. This study describes proteome changes from sera of...
AbstractContextFatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown. ObjectivesThis study describes...
Fatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown.CONTEXTFatigue is the most distressing side effect of...
Context Fatigue is the most distressing side effect of radiation therapy, and its progression etiology is unknown. Objectives This study describes proteome...
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Enrichment Source
Publisher
StartPage 748
SubjectTerms Aetiology
Aged
Anesthesia
Apolipoprotein A-I - blood
Apolipoproteins E - blood
Biological and medical sciences
Blotting, Western
Chromatography, Liquid
Disease Progression
External beam radiation therapy
Fatigue
Fatigue - blood
Fatigue - etiology
Gynecology. Andrology. Obstetrics
Humans
Male
Male genital diseases
Medical sciences
Middle Aged
Multiple tumors. Solid tumors. Tumors in childhood (general aspects)
Nephrology. Urinary tract diseases
Pain Medicine
Pharmacology. Drug treatments
Prealbumin - metabolism
prostate cancer
Prostatic cancer
Prostatic Neoplasms - blood
Prostatic Neoplasms - radiotherapy
Proteins
Proteomics - methods
quantitative proteomics
Radiation
Serum
Severity of Illness Index
Tandem Mass Spectrometry
Time Factors
Tumors
Tumors of the urinary system
Two-Dimensional Difference Gel Electrophoresis
Urinary tract. Prostate gland
Western blot
Title Proteomic Serum Profile of Fatigued Men Receiving Localized External Beam Radiation Therapy for Non-Metastatic Prostate Cancer
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0885392413003333
https://www.clinicalkey.es/playcontent/1-s2.0-S0885392413003333
https://dx.doi.org/10.1016/j.jpainsymman.2013.05.016
https://www.ncbi.nlm.nih.gov/pubmed/23916682
https://www.proquest.com/docview/1516724252
https://www.proquest.com/docview/1541974915
https://pubmed.ncbi.nlm.nih.gov/PMC3743082
http://www.jpsmjournal.com/article/S0885392413003333/pdf
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