Cargando…
Neurotrophin-3 (NT-3) as a Potential Biomarker of the Peripheral Nervous System Damage Following Breast Cancer Treatment
Damage to the peripheral nervous system (PNS) is a common complication of breast cancer (BC) treatment, with 60 to 80% of breast cancer survivors experiencing symptoms of PNS damage. In the current study, the levels of brain-derived neurotrophic factor (BDNF), galectin-3 (Gal-3), and neurotrophin-3...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123681/ https://www.ncbi.nlm.nih.gov/pubmed/37092524 http://dx.doi.org/10.3390/pathophysiology30020010 |
_version_ | 1785029709565788160 |
---|---|
author | Tonyan, Samvel Pospelova, Maria Krasnikova, Varvara Fionik, Olga Alekseeva, Tatyana Samochernykh, Konstantin Ivanova, Nataliya Vavilova, Tatyana Vasilieva, Elena Makhanova, Albina Nikolaeva, Aleksandra Bukkieva, Tatyana Combs, Stephanie Shevtsov, Maxim |
author_facet | Tonyan, Samvel Pospelova, Maria Krasnikova, Varvara Fionik, Olga Alekseeva, Tatyana Samochernykh, Konstantin Ivanova, Nataliya Vavilova, Tatyana Vasilieva, Elena Makhanova, Albina Nikolaeva, Aleksandra Bukkieva, Tatyana Combs, Stephanie Shevtsov, Maxim |
author_sort | Tonyan, Samvel |
collection | PubMed |
description | Damage to the peripheral nervous system (PNS) is a common complication of breast cancer (BC) treatment, with 60 to 80% of breast cancer survivors experiencing symptoms of PNS damage. In the current study, the levels of brain-derived neurotrophic factor (BDNF), galectin-3 (Gal-3), and neurotrophin-3 (NT-3) were measured in the blood serum of BC patients by ELISA as potential biomarkers that might indicate the PNS damage. Sixty-seven patients were enrolled in this multi-center trial and compared to the aged-matched healthy female volunteers (control group) (n = 25). Intergroup comparison of biomarker levels (i.e., Gal-3 and BDNF) did not show significant differences in any of the studied subgroups. However, intriguingly, NT-3 levels were significantly higher in BC patients as compared to healthy volunteers, constituting 14.85 [10.3; 18.0] and 5.74 [4.56; 13.7] pg/mL, respectively (p < 0.001). In conclusion, NT-3 might be employed as a potential biomarker in BC patients with clinical manifestations of PNS damage. However, further studies to validate its correlation to the degree of peripheral nervous system lesions are of high value. |
format | Online Article Text |
id | pubmed-10123681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101236812023-04-25 Neurotrophin-3 (NT-3) as a Potential Biomarker of the Peripheral Nervous System Damage Following Breast Cancer Treatment Tonyan, Samvel Pospelova, Maria Krasnikova, Varvara Fionik, Olga Alekseeva, Tatyana Samochernykh, Konstantin Ivanova, Nataliya Vavilova, Tatyana Vasilieva, Elena Makhanova, Albina Nikolaeva, Aleksandra Bukkieva, Tatyana Combs, Stephanie Shevtsov, Maxim Pathophysiology Article Damage to the peripheral nervous system (PNS) is a common complication of breast cancer (BC) treatment, with 60 to 80% of breast cancer survivors experiencing symptoms of PNS damage. In the current study, the levels of brain-derived neurotrophic factor (BDNF), galectin-3 (Gal-3), and neurotrophin-3 (NT-3) were measured in the blood serum of BC patients by ELISA as potential biomarkers that might indicate the PNS damage. Sixty-seven patients were enrolled in this multi-center trial and compared to the aged-matched healthy female volunteers (control group) (n = 25). Intergroup comparison of biomarker levels (i.e., Gal-3 and BDNF) did not show significant differences in any of the studied subgroups. However, intriguingly, NT-3 levels were significantly higher in BC patients as compared to healthy volunteers, constituting 14.85 [10.3; 18.0] and 5.74 [4.56; 13.7] pg/mL, respectively (p < 0.001). In conclusion, NT-3 might be employed as a potential biomarker in BC patients with clinical manifestations of PNS damage. However, further studies to validate its correlation to the degree of peripheral nervous system lesions are of high value. MDPI 2023-04-03 /pmc/articles/PMC10123681/ /pubmed/37092524 http://dx.doi.org/10.3390/pathophysiology30020010 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tonyan, Samvel Pospelova, Maria Krasnikova, Varvara Fionik, Olga Alekseeva, Tatyana Samochernykh, Konstantin Ivanova, Nataliya Vavilova, Tatyana Vasilieva, Elena Makhanova, Albina Nikolaeva, Aleksandra Bukkieva, Tatyana Combs, Stephanie Shevtsov, Maxim Neurotrophin-3 (NT-3) as a Potential Biomarker of the Peripheral Nervous System Damage Following Breast Cancer Treatment |
title | Neurotrophin-3 (NT-3) as a Potential Biomarker of the Peripheral Nervous System Damage Following Breast Cancer Treatment |
title_full | Neurotrophin-3 (NT-3) as a Potential Biomarker of the Peripheral Nervous System Damage Following Breast Cancer Treatment |
title_fullStr | Neurotrophin-3 (NT-3) as a Potential Biomarker of the Peripheral Nervous System Damage Following Breast Cancer Treatment |
title_full_unstemmed | Neurotrophin-3 (NT-3) as a Potential Biomarker of the Peripheral Nervous System Damage Following Breast Cancer Treatment |
title_short | Neurotrophin-3 (NT-3) as a Potential Biomarker of the Peripheral Nervous System Damage Following Breast Cancer Treatment |
title_sort | neurotrophin-3 (nt-3) as a potential biomarker of the peripheral nervous system damage following breast cancer treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123681/ https://www.ncbi.nlm.nih.gov/pubmed/37092524 http://dx.doi.org/10.3390/pathophysiology30020010 |
work_keys_str_mv | AT tonyansamvel neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT pospelovamaria neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT krasnikovavarvara neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT fionikolga neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT alekseevatatyana neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT samochernykhkonstantin neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT ivanovanataliya neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT vavilovatatyana neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT vasilievaelena neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT makhanovaalbina neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT nikolaevaaleksandra neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT bukkievatatyana neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT combsstephanie neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment AT shevtsovmaxim neurotrophin3nt3asapotentialbiomarkeroftheperipheralnervoussystemdamagefollowingbreastcancertreatment |