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Differences in Circulating Extracellular Vesicle and Soluble Cytokines in Older Versus Younger Breast Cancer Patients With Distinct Symptom Profiles

Because extracellular vesicle (EV)-associated cytokines, both encapsulated and surface bound, have been associated with symptom severity, and may vary over the lifespan, they may be potential biomarkers to uncover underlying mechanisms of various conditions. This study evaluated the associations of...

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Autores principales: Sass, Dilorom, Fitzgerald, Wendy, Wolff, Brian S., Torres, Isaias, Pagan-Mercado, Glorivee, Armstrong, Terri S., Miaskowski, Christine, Margolis, Leonid, Saligan, Leorey, Kober, Kord M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081604/
https://www.ncbi.nlm.nih.gov/pubmed/35547250
http://dx.doi.org/10.3389/fgene.2022.869044
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author Sass, Dilorom
Fitzgerald, Wendy
Wolff, Brian S.
Torres, Isaias
Pagan-Mercado, Glorivee
Armstrong, Terri S.
Miaskowski, Christine
Margolis, Leonid
Saligan, Leorey
Kober, Kord M.
author_facet Sass, Dilorom
Fitzgerald, Wendy
Wolff, Brian S.
Torres, Isaias
Pagan-Mercado, Glorivee
Armstrong, Terri S.
Miaskowski, Christine
Margolis, Leonid
Saligan, Leorey
Kober, Kord M.
author_sort Sass, Dilorom
collection PubMed
description Because extracellular vesicle (EV)-associated cytokines, both encapsulated and surface bound, have been associated with symptom severity, and may vary over the lifespan, they may be potential biomarkers to uncover underlying mechanisms of various conditions. This study evaluated the associations of soluble and EV-associated cytokine concentrations with distinct symptom profiles reported by 290 women with breast cancer prior to surgery. Patients were classified into older (≥60 years, n = 93) and younger (< 60 years, n = 197) cohorts within two previously identified distinct symptom severity profiles, that included pain, depressive symptoms, sleep disturbance, and fatigue (i.e., High Fatigue Low Pain and All Low). EVs were extracted using ExoQuick. Cytokine concentrations were determined using Luminex multiplex assay. Mann Whitney U test evaluated the differences in EV and soluble cytokine levels between symptom classes and between and within the older and younger cohorts adjusting for Karnofsky Performance Status (KPS) score, body mass index (BMI), and stage of disease. Partial correlation analyses were run between symptom severity scores and cytokine concentrations. Results of this study suggest that levels of cytokine concentrations differ between EV and soluble fractions. Several EV and soluble pro-inflammatory cytokines had positive associations with depressive symptoms and fatigue within both age cohorts and symptom profiles. In addition, in the older cohort with High Fatigue Low Pain symptom profile, EV GM-CSF concentrations were higher compared to the All Low symptom profile (p < 0.05). Albeit limited by a small sample size, these exploratory analyses provide new information on the association between cytokines and symptom profiles of older and younger cohorts. Of note, unique EV-associated cytokines were found in older patients and in specific symptom classes. These results suggest that EVs may be potential biomarker discovery tools. Understanding the mechanisms that underlie distinct symptom class profiles categorized by age may inform intervention trials and offer precision medicine approaches.
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spelling pubmed-90816042022-05-10 Differences in Circulating Extracellular Vesicle and Soluble Cytokines in Older Versus Younger Breast Cancer Patients With Distinct Symptom Profiles Sass, Dilorom Fitzgerald, Wendy Wolff, Brian S. Torres, Isaias Pagan-Mercado, Glorivee Armstrong, Terri S. Miaskowski, Christine Margolis, Leonid Saligan, Leorey Kober, Kord M. Front Genet Genetics Because extracellular vesicle (EV)-associated cytokines, both encapsulated and surface bound, have been associated with symptom severity, and may vary over the lifespan, they may be potential biomarkers to uncover underlying mechanisms of various conditions. This study evaluated the associations of soluble and EV-associated cytokine concentrations with distinct symptom profiles reported by 290 women with breast cancer prior to surgery. Patients were classified into older (≥60 years, n = 93) and younger (< 60 years, n = 197) cohorts within two previously identified distinct symptom severity profiles, that included pain, depressive symptoms, sleep disturbance, and fatigue (i.e., High Fatigue Low Pain and All Low). EVs were extracted using ExoQuick. Cytokine concentrations were determined using Luminex multiplex assay. Mann Whitney U test evaluated the differences in EV and soluble cytokine levels between symptom classes and between and within the older and younger cohorts adjusting for Karnofsky Performance Status (KPS) score, body mass index (BMI), and stage of disease. Partial correlation analyses were run between symptom severity scores and cytokine concentrations. Results of this study suggest that levels of cytokine concentrations differ between EV and soluble fractions. Several EV and soluble pro-inflammatory cytokines had positive associations with depressive symptoms and fatigue within both age cohorts and symptom profiles. In addition, in the older cohort with High Fatigue Low Pain symptom profile, EV GM-CSF concentrations were higher compared to the All Low symptom profile (p < 0.05). Albeit limited by a small sample size, these exploratory analyses provide new information on the association between cytokines and symptom profiles of older and younger cohorts. Of note, unique EV-associated cytokines were found in older patients and in specific symptom classes. These results suggest that EVs may be potential biomarker discovery tools. Understanding the mechanisms that underlie distinct symptom class profiles categorized by age may inform intervention trials and offer precision medicine approaches. Frontiers Media S.A. 2022-04-25 /pmc/articles/PMC9081604/ /pubmed/35547250 http://dx.doi.org/10.3389/fgene.2022.869044 Text en Copyright © 2022 Sass, Fitzgerald, Wolff, Torres, Pagan-Mercado, Armstrong, Miaskowski, Margolis, Saligan and Kober. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Sass, Dilorom
Fitzgerald, Wendy
Wolff, Brian S.
Torres, Isaias
Pagan-Mercado, Glorivee
Armstrong, Terri S.
Miaskowski, Christine
Margolis, Leonid
Saligan, Leorey
Kober, Kord M.
Differences in Circulating Extracellular Vesicle and Soluble Cytokines in Older Versus Younger Breast Cancer Patients With Distinct Symptom Profiles
title Differences in Circulating Extracellular Vesicle and Soluble Cytokines in Older Versus Younger Breast Cancer Patients With Distinct Symptom Profiles
title_full Differences in Circulating Extracellular Vesicle and Soluble Cytokines in Older Versus Younger Breast Cancer Patients With Distinct Symptom Profiles
title_fullStr Differences in Circulating Extracellular Vesicle and Soluble Cytokines in Older Versus Younger Breast Cancer Patients With Distinct Symptom Profiles
title_full_unstemmed Differences in Circulating Extracellular Vesicle and Soluble Cytokines in Older Versus Younger Breast Cancer Patients With Distinct Symptom Profiles
title_short Differences in Circulating Extracellular Vesicle and Soluble Cytokines in Older Versus Younger Breast Cancer Patients With Distinct Symptom Profiles
title_sort differences in circulating extracellular vesicle and soluble cytokines in older versus younger breast cancer patients with distinct symptom profiles
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081604/
https://www.ncbi.nlm.nih.gov/pubmed/35547250
http://dx.doi.org/10.3389/fgene.2022.869044
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