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High Expression of microRNA-143 is Associated with Favorable Tumor Immune Microenvironment and Better Survival in Estrogen Receptor Positive Breast Cancer

microRNA-143 (miR-143) is a well-known tumor suppressive microRNA that exhibits anti-tumoral function by targeting KRAS signaling pathways in various malignancies. We hypothesized that miR-143 suppresses breast cancer progression by targeting KRAS and its effector molecules. We further hypothesized...

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Autores principales: Tokumaru, Yoshihisa, Asaoka, Mariko, Oshi, Masanori, Katsuta, Eriko, Yan, Li, Narayanan, Sumana, Sugito, Nobuhiko, Matsuhashi, Nobuhisa, Futamura, Manabu, Akao, Yukihiro, Yoshida, Kazuhiro, Takabe, Kazuaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246786/
https://www.ncbi.nlm.nih.gov/pubmed/32370060
http://dx.doi.org/10.3390/ijms21093213
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author Tokumaru, Yoshihisa
Asaoka, Mariko
Oshi, Masanori
Katsuta, Eriko
Yan, Li
Narayanan, Sumana
Sugito, Nobuhiko
Matsuhashi, Nobuhisa
Futamura, Manabu
Akao, Yukihiro
Yoshida, Kazuhiro
Takabe, Kazuaki
author_facet Tokumaru, Yoshihisa
Asaoka, Mariko
Oshi, Masanori
Katsuta, Eriko
Yan, Li
Narayanan, Sumana
Sugito, Nobuhiko
Matsuhashi, Nobuhisa
Futamura, Manabu
Akao, Yukihiro
Yoshida, Kazuhiro
Takabe, Kazuaki
author_sort Tokumaru, Yoshihisa
collection PubMed
description microRNA-143 (miR-143) is a well-known tumor suppressive microRNA that exhibits anti-tumoral function by targeting KRAS signaling pathways in various malignancies. We hypothesized that miR-143 suppresses breast cancer progression by targeting KRAS and its effector molecules. We further hypothesized that high expression of miR-143 is associated with a favorable tumor immune microenvironment of estrogen receptor (ER)-positive breast cancer patients which result in improved survival. Two major publicly available breast cancer cohorts; The Cancer Genome Atlas (TCGA) and Molecular Taxonomy of Breast Cancer International Consortium (METABRIC) were used. The miR-143 high expression group was associated with increased infiltration of anti-cancer immune cells and decreased pro-cancer immune cells, as well as enrichment of the genes relating to T helper (Th1) cells resulting in improved overall survival (OS) in ER-positive breast cancer patients. To the best of our knowledge, this is the first study to demonstrate that high expression of miR-143 in cancer cells associates with a favorable tumor immune microenvironment, upregulation of anti-cancer immune cells, and suppression of the pro-cancer immune cells, associating with better survival of the breast cancer patients.
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spelling pubmed-72467862020-06-10 High Expression of microRNA-143 is Associated with Favorable Tumor Immune Microenvironment and Better Survival in Estrogen Receptor Positive Breast Cancer Tokumaru, Yoshihisa Asaoka, Mariko Oshi, Masanori Katsuta, Eriko Yan, Li Narayanan, Sumana Sugito, Nobuhiko Matsuhashi, Nobuhisa Futamura, Manabu Akao, Yukihiro Yoshida, Kazuhiro Takabe, Kazuaki Int J Mol Sci Article microRNA-143 (miR-143) is a well-known tumor suppressive microRNA that exhibits anti-tumoral function by targeting KRAS signaling pathways in various malignancies. We hypothesized that miR-143 suppresses breast cancer progression by targeting KRAS and its effector molecules. We further hypothesized that high expression of miR-143 is associated with a favorable tumor immune microenvironment of estrogen receptor (ER)-positive breast cancer patients which result in improved survival. Two major publicly available breast cancer cohorts; The Cancer Genome Atlas (TCGA) and Molecular Taxonomy of Breast Cancer International Consortium (METABRIC) were used. The miR-143 high expression group was associated with increased infiltration of anti-cancer immune cells and decreased pro-cancer immune cells, as well as enrichment of the genes relating to T helper (Th1) cells resulting in improved overall survival (OS) in ER-positive breast cancer patients. To the best of our knowledge, this is the first study to demonstrate that high expression of miR-143 in cancer cells associates with a favorable tumor immune microenvironment, upregulation of anti-cancer immune cells, and suppression of the pro-cancer immune cells, associating with better survival of the breast cancer patients. MDPI 2020-05-01 /pmc/articles/PMC7246786/ /pubmed/32370060 http://dx.doi.org/10.3390/ijms21093213 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tokumaru, Yoshihisa
Asaoka, Mariko
Oshi, Masanori
Katsuta, Eriko
Yan, Li
Narayanan, Sumana
Sugito, Nobuhiko
Matsuhashi, Nobuhisa
Futamura, Manabu
Akao, Yukihiro
Yoshida, Kazuhiro
Takabe, Kazuaki
High Expression of microRNA-143 is Associated with Favorable Tumor Immune Microenvironment and Better Survival in Estrogen Receptor Positive Breast Cancer
title High Expression of microRNA-143 is Associated with Favorable Tumor Immune Microenvironment and Better Survival in Estrogen Receptor Positive Breast Cancer
title_full High Expression of microRNA-143 is Associated with Favorable Tumor Immune Microenvironment and Better Survival in Estrogen Receptor Positive Breast Cancer
title_fullStr High Expression of microRNA-143 is Associated with Favorable Tumor Immune Microenvironment and Better Survival in Estrogen Receptor Positive Breast Cancer
title_full_unstemmed High Expression of microRNA-143 is Associated with Favorable Tumor Immune Microenvironment and Better Survival in Estrogen Receptor Positive Breast Cancer
title_short High Expression of microRNA-143 is Associated with Favorable Tumor Immune Microenvironment and Better Survival in Estrogen Receptor Positive Breast Cancer
title_sort high expression of microrna-143 is associated with favorable tumor immune microenvironment and better survival in estrogen receptor positive breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246786/
https://www.ncbi.nlm.nih.gov/pubmed/32370060
http://dx.doi.org/10.3390/ijms21093213
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