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 in | Journal of pain and symptom management Vol. 47; no. 4; pp. 748 - 756.e4 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Elsevier Inc
01.04.2014
Elsevier |
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Online Access | Get full text |
ISSN | 0885-3924 1873-6513 1873-6513 |
DOI | 10.1016/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. |
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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 |
Author_xml | – sequence: 1 givenname: Nada surname: Lukkahatai fullname: Lukkahatai, Nada email: nada.lukkahatai@nih.gov organization: National Institute of Nursing Research, National Institutes of Health, Bethesda, Maryland, USA – sequence: 2 givenname: Sajni surname: Patel fullname: Patel, Sajni organization: National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA – sequence: 3 givenname: Marjan surname: Gucek fullname: Gucek, Marjan organization: National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA – sequence: 4 givenname: Chao-Pin surname: Hsiao fullname: Hsiao, Chao-Pin organization: National Institute of Nursing Research, National Institutes of Health, Bethesda, Maryland, USA – sequence: 5 givenname: Leorey N. surname: Saligan fullname: Saligan, Leorey N. organization: National Institute of Nursing Research, National Institutes of Health, Bethesda, Maryland, USA |
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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 |
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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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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 |
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