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MicroRNA-200c and microRNA- 141 are regulated by a FOXP3-KAT2B axis and associated with tumor metastasis in breast cancer

BACKGROUND: Members of the microRNA (miR)-200 family, which are involved in tumor metastasis, have potential as cancer biomarkers, but their regulatory mechanisms remain elusive. METHODS: We investigated FOXP3-inducible breast cancer cells, Foxp3 heterozygous Scurfy mutant (Foxp3 (sf/+)) female mice...

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Autores principales: Zhang, Guangxin, Zhang, Wei, Li, Bingjin, Stringer-Reasor, Erica, Chu, Chengjing, Sun, Liyan, Bae, Sejong, Chen, Dongquan, Wei, Shi, Jiao, Kenneth, Yang, Wei-Hsiung, Cui, Ranji, Liu, Runhua, Wang, Lizhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480201/
https://www.ncbi.nlm.nih.gov/pubmed/28637482
http://dx.doi.org/10.1186/s13058-017-0858-x
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author Zhang, Guangxin
Zhang, Wei
Li, Bingjin
Stringer-Reasor, Erica
Chu, Chengjing
Sun, Liyan
Bae, Sejong
Chen, Dongquan
Wei, Shi
Jiao, Kenneth
Yang, Wei-Hsiung
Cui, Ranji
Liu, Runhua
Wang, Lizhong
author_facet Zhang, Guangxin
Zhang, Wei
Li, Bingjin
Stringer-Reasor, Erica
Chu, Chengjing
Sun, Liyan
Bae, Sejong
Chen, Dongquan
Wei, Shi
Jiao, Kenneth
Yang, Wei-Hsiung
Cui, Ranji
Liu, Runhua
Wang, Lizhong
author_sort Zhang, Guangxin
collection PubMed
description BACKGROUND: Members of the microRNA (miR)-200 family, which are involved in tumor metastasis, have potential as cancer biomarkers, but their regulatory mechanisms remain elusive. METHODS: We investigated FOXP3-inducible breast cancer cells, Foxp3 heterozygous Scurfy mutant (Foxp3 (sf/+)) female mice, and patients with breast cancer for characterization of the formation and regulation of the miR-200 family in breast cancer cells and circulation. Participants (259), including patients with breast cancer or benign breast tumors, members of breast cancer families, and healthy controls, were assessed for tumor and circulating levels of the miR-200 family. RESULTS: First, we identified a FOXP3-KAT2B-miR-200c/141 axis in breast cancer cells. Second, aging Foxp3 (sf/+) female mice developed spontaneous breast cancers and lung metastases. Levels of miR-200c and miR-141 were lower in Foxp3 (sf/+) tumor cells than in normal breast epithelial cells, but plasma levels of miR-200c and miR-141 in the Foxp3 (sf/+) mice increased during tumor progression and metastasis. Third, in patients with breast cancer, the levels of miR-200c and 141 were lower in FOXP3 (low) relative to those with FOXP3 (high) breast cancer cells, especially in late-stage and metastatic cancer cells. The levels of miR-200c and miR-141 were higher in plasma from patients with metastatic breast cancer than in plasma from those with localized breast cancer, with benign breast tumors, with a family history of breast cancer, or from healthy controls. Finally, in Foxp3 (sf/+) mice, plasma miR-200c and miR-141 appeared to be released from tumor cells. CONCLUSIONS: miR-200c and miR-141 are regulated by a FOXP3-KAT2B axis in breast cancer cells, and circulating levels of miR-200c and miR-141 are potential biomarkers for early detection of breast cancer metastases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-017-0858-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-54802012017-06-23 MicroRNA-200c and microRNA- 141 are regulated by a FOXP3-KAT2B axis and associated with tumor metastasis in breast cancer Zhang, Guangxin Zhang, Wei Li, Bingjin Stringer-Reasor, Erica Chu, Chengjing Sun, Liyan Bae, Sejong Chen, Dongquan Wei, Shi Jiao, Kenneth Yang, Wei-Hsiung Cui, Ranji Liu, Runhua Wang, Lizhong Breast Cancer Res Research Article BACKGROUND: Members of the microRNA (miR)-200 family, which are involved in tumor metastasis, have potential as cancer biomarkers, but their regulatory mechanisms remain elusive. METHODS: We investigated FOXP3-inducible breast cancer cells, Foxp3 heterozygous Scurfy mutant (Foxp3 (sf/+)) female mice, and patients with breast cancer for characterization of the formation and regulation of the miR-200 family in breast cancer cells and circulation. Participants (259), including patients with breast cancer or benign breast tumors, members of breast cancer families, and healthy controls, were assessed for tumor and circulating levels of the miR-200 family. RESULTS: First, we identified a FOXP3-KAT2B-miR-200c/141 axis in breast cancer cells. Second, aging Foxp3 (sf/+) female mice developed spontaneous breast cancers and lung metastases. Levels of miR-200c and miR-141 were lower in Foxp3 (sf/+) tumor cells than in normal breast epithelial cells, but plasma levels of miR-200c and miR-141 in the Foxp3 (sf/+) mice increased during tumor progression and metastasis. Third, in patients with breast cancer, the levels of miR-200c and 141 were lower in FOXP3 (low) relative to those with FOXP3 (high) breast cancer cells, especially in late-stage and metastatic cancer cells. The levels of miR-200c and miR-141 were higher in plasma from patients with metastatic breast cancer than in plasma from those with localized breast cancer, with benign breast tumors, with a family history of breast cancer, or from healthy controls. Finally, in Foxp3 (sf/+) mice, plasma miR-200c and miR-141 appeared to be released from tumor cells. CONCLUSIONS: miR-200c and miR-141 are regulated by a FOXP3-KAT2B axis in breast cancer cells, and circulating levels of miR-200c and miR-141 are potential biomarkers for early detection of breast cancer metastases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-017-0858-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-21 2017 /pmc/articles/PMC5480201/ /pubmed/28637482 http://dx.doi.org/10.1186/s13058-017-0858-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhang, Guangxin
Zhang, Wei
Li, Bingjin
Stringer-Reasor, Erica
Chu, Chengjing
Sun, Liyan
Bae, Sejong
Chen, Dongquan
Wei, Shi
Jiao, Kenneth
Yang, Wei-Hsiung
Cui, Ranji
Liu, Runhua
Wang, Lizhong
MicroRNA-200c and microRNA- 141 are regulated by a FOXP3-KAT2B axis and associated with tumor metastasis in breast cancer
title MicroRNA-200c and microRNA- 141 are regulated by a FOXP3-KAT2B axis and associated with tumor metastasis in breast cancer
title_full MicroRNA-200c and microRNA- 141 are regulated by a FOXP3-KAT2B axis and associated with tumor metastasis in breast cancer
title_fullStr MicroRNA-200c and microRNA- 141 are regulated by a FOXP3-KAT2B axis and associated with tumor metastasis in breast cancer
title_full_unstemmed MicroRNA-200c and microRNA- 141 are regulated by a FOXP3-KAT2B axis and associated with tumor metastasis in breast cancer
title_short MicroRNA-200c and microRNA- 141 are regulated by a FOXP3-KAT2B axis and associated with tumor metastasis in breast cancer
title_sort microrna-200c and microrna- 141 are regulated by a foxp3-kat2b axis and associated with tumor metastasis in breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480201/
https://www.ncbi.nlm.nih.gov/pubmed/28637482
http://dx.doi.org/10.1186/s13058-017-0858-x
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