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Dynamic Changes of Circulating Mir-155 Expression and the Potential Application as a Non-Invasive Biomarker in Breast Cancer

BACKGROUND: Breast cancer incidence rates have been continuously increasing in majority nations with significant higher portion of cancer-related mortality in low- and middle-income countries. Developing new biomarker is an emerging field in the breast cancer research. Application of a promising min...

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Autores principales: Anwar, Sumadi Lukman, Tanjung, Dewi Sahfitri, Fitria, Meutia Srikandi, Kartika, Aprilia Indra, Sari, Dwi Nur Indah, Rakhmina, Dinna, Wardana, Tirta, Astuti, Indwiani, Haryana, Sofia Mubarika, Aryandono, Teguh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332147/
https://www.ncbi.nlm.nih.gov/pubmed/32102529
http://dx.doi.org/10.31557/APJCP.2020.21.2.491
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author Anwar, Sumadi Lukman
Tanjung, Dewi Sahfitri
Fitria, Meutia Srikandi
Kartika, Aprilia Indra
Sari, Dwi Nur Indah
Rakhmina, Dinna
Wardana, Tirta
Astuti, Indwiani
Haryana, Sofia Mubarika
Aryandono, Teguh
author_facet Anwar, Sumadi Lukman
Tanjung, Dewi Sahfitri
Fitria, Meutia Srikandi
Kartika, Aprilia Indra
Sari, Dwi Nur Indah
Rakhmina, Dinna
Wardana, Tirta
Astuti, Indwiani
Haryana, Sofia Mubarika
Aryandono, Teguh
author_sort Anwar, Sumadi Lukman
collection PubMed
description BACKGROUND: Breast cancer incidence rates have been continuously increasing in majority nations with significant higher portion of cancer-related mortality in low- and middle-income countries. Developing new biomarker is an emerging field in the breast cancer research. Application of a promising minimally invasive biomarker, circulating microRNA, for additional improvement of diagnosis, prognosis, and therapeutic monitoring in breast cancer is not well corroborated. MATERIALS AND METHODS: To uncover the potential use of circulating miR-155 expression as a clinical biomarker in breast cancer, we analyzed 102 breast cancer patients at diagnosis and after treatment as well as 15 healthy women. Total RNA was isolated from patient’s plasma and expression of circulating miR-155 was measured with quantitative reverse transcription polymerase chain reaction (qRT-PCR). The expression levels of circulating miR-155 were compared according to the effect of treatment, clinicopathological variables, and progression-free survival. RESULTS: In comparison to the healthy women, expression of circulating miR-155 levels were significantly higher (medians were 18.49±19 and 1.28±0.18, respectively; p<0.0001). The expression levels of miR-155 were significantly diminished after patients completed surgery and chemotherapy (medians were 18.49±19 at diagnosis and 1.32±0.22 after treatment, respectively; p<0.0001). Patients older than 40 years old expressed higher circulating miR-155 than those younger than 40 years-old (medians were 28.92±22 and 4.19±2.49, respectively; p<0.0001). Circulating miR-155 was significantly higher in patients with tumors larger than 5 cm (44.27±2.6 vs 9.17±6.9, p=0.03). MiR-155 expression levels were not significantly different according to various tumor grades, subtypes, and clinical stages. Although longer follow-up is required, progression-free survivals of patients with upregulation of circulating miR-155 were significantly longer (mean survivals were 77 and 65 weeks, Log-rank (Mantel-Cox) test p=0.038). CONCLUSION: Expression of circulating miR-155 expression was significantly elevated in breast cancer patients and was decreased after treatment. Therefore, circulating miR-155 is potentially applicable as diagnostic therapeutic monitoring marker in breast cancer.
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spelling pubmed-73321472020-07-07 Dynamic Changes of Circulating Mir-155 Expression and the Potential Application as a Non-Invasive Biomarker in Breast Cancer Anwar, Sumadi Lukman Tanjung, Dewi Sahfitri Fitria, Meutia Srikandi Kartika, Aprilia Indra Sari, Dwi Nur Indah Rakhmina, Dinna Wardana, Tirta Astuti, Indwiani Haryana, Sofia Mubarika Aryandono, Teguh Asian Pac J Cancer Prev Research Article BACKGROUND: Breast cancer incidence rates have been continuously increasing in majority nations with significant higher portion of cancer-related mortality in low- and middle-income countries. Developing new biomarker is an emerging field in the breast cancer research. Application of a promising minimally invasive biomarker, circulating microRNA, for additional improvement of diagnosis, prognosis, and therapeutic monitoring in breast cancer is not well corroborated. MATERIALS AND METHODS: To uncover the potential use of circulating miR-155 expression as a clinical biomarker in breast cancer, we analyzed 102 breast cancer patients at diagnosis and after treatment as well as 15 healthy women. Total RNA was isolated from patient’s plasma and expression of circulating miR-155 was measured with quantitative reverse transcription polymerase chain reaction (qRT-PCR). The expression levels of circulating miR-155 were compared according to the effect of treatment, clinicopathological variables, and progression-free survival. RESULTS: In comparison to the healthy women, expression of circulating miR-155 levels were significantly higher (medians were 18.49±19 and 1.28±0.18, respectively; p<0.0001). The expression levels of miR-155 were significantly diminished after patients completed surgery and chemotherapy (medians were 18.49±19 at diagnosis and 1.32±0.22 after treatment, respectively; p<0.0001). Patients older than 40 years old expressed higher circulating miR-155 than those younger than 40 years-old (medians were 28.92±22 and 4.19±2.49, respectively; p<0.0001). Circulating miR-155 was significantly higher in patients with tumors larger than 5 cm (44.27±2.6 vs 9.17±6.9, p=0.03). MiR-155 expression levels were not significantly different according to various tumor grades, subtypes, and clinical stages. Although longer follow-up is required, progression-free survivals of patients with upregulation of circulating miR-155 were significantly longer (mean survivals were 77 and 65 weeks, Log-rank (Mantel-Cox) test p=0.038). CONCLUSION: Expression of circulating miR-155 expression was significantly elevated in breast cancer patients and was decreased after treatment. Therefore, circulating miR-155 is potentially applicable as diagnostic therapeutic monitoring marker in breast cancer. West Asia Organization for Cancer Prevention 2020 /pmc/articles/PMC7332147/ /pubmed/32102529 http://dx.doi.org/10.31557/APJCP.2020.21.2.491 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Anwar, Sumadi Lukman
Tanjung, Dewi Sahfitri
Fitria, Meutia Srikandi
Kartika, Aprilia Indra
Sari, Dwi Nur Indah
Rakhmina, Dinna
Wardana, Tirta
Astuti, Indwiani
Haryana, Sofia Mubarika
Aryandono, Teguh
Dynamic Changes of Circulating Mir-155 Expression and the Potential Application as a Non-Invasive Biomarker in Breast Cancer
title Dynamic Changes of Circulating Mir-155 Expression and the Potential Application as a Non-Invasive Biomarker in Breast Cancer
title_full Dynamic Changes of Circulating Mir-155 Expression and the Potential Application as a Non-Invasive Biomarker in Breast Cancer
title_fullStr Dynamic Changes of Circulating Mir-155 Expression and the Potential Application as a Non-Invasive Biomarker in Breast Cancer
title_full_unstemmed Dynamic Changes of Circulating Mir-155 Expression and the Potential Application as a Non-Invasive Biomarker in Breast Cancer
title_short Dynamic Changes of Circulating Mir-155 Expression and the Potential Application as a Non-Invasive Biomarker in Breast Cancer
title_sort dynamic changes of circulating mir-155 expression and the potential application as a non-invasive biomarker in breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332147/
https://www.ncbi.nlm.nih.gov/pubmed/32102529
http://dx.doi.org/10.31557/APJCP.2020.21.2.491
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