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Anterior Gradient 3 Promotes Breast Cancer Development and Chemotherapy Response

PURPOSE: Anterior gradient 3 (AGR3) belongs to human anterior gradient (AGR) family. The function of AGR3 on cancer remains unknown. This research aimed to investigate if AGR3 had prognostic values in invasive ductal carcinoma (IDC) of breast cancer and could promote tumor progression. MATERIALS AND...

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Autores principales: Xu, Qiao, Shao, Ying, Zhang, Jinman, Zhang, Huikun, Zhao, Yawen, Liu, Xiaoli, Guo, Zhifang, Chong, Wei, Gu, Feng, Ma, Yongjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Cancer Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962492/
https://www.ncbi.nlm.nih.gov/pubmed/31291711
http://dx.doi.org/10.4143/crt.2019.217
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author Xu, Qiao
Shao, Ying
Zhang, Jinman
Zhang, Huikun
Zhao, Yawen
Liu, Xiaoli
Guo, Zhifang
Chong, Wei
Gu, Feng
Ma, Yongjie
author_facet Xu, Qiao
Shao, Ying
Zhang, Jinman
Zhang, Huikun
Zhao, Yawen
Liu, Xiaoli
Guo, Zhifang
Chong, Wei
Gu, Feng
Ma, Yongjie
author_sort Xu, Qiao
collection PubMed
description PURPOSE: Anterior gradient 3 (AGR3) belongs to human anterior gradient (AGR) family. The function of AGR3 on cancer remains unknown. This research aimed to investigate if AGR3 had prognostic values in invasive ductal carcinoma (IDC) of breast cancer and could promote tumor progression. MATERIALS AND METHODS: AGR3 expression was detected in breast benign lesions, ductal carcinoma in situ and IDC by immunohistochemistry analysis. AGR3’s correlations with clinicopathological features and prognosis of IDC patients were analyzed. By cell function experiments, collagen gel droplet-embedded culture drug sensitivity test and cytotoxic analysis, AGR3’s impacts on proliferation, invasion ability, and chemotherapeutic drug sensitivity of breast cancer cells were also detected. RESULTS: AGR3 was up-regulated in luminal subtype of histological grade I-II of IDC patients and positively correlated with high risks of recurrence and distant metastasis. AGR3 high expression could lead to bone or liver metastasis and predict poor prognosis of luminal B. In cell lines, AGR3 could promote proliferation and invasion ability of breast cancer cells which were consistent with clinical analysis. Besides, AGR3 could indicate poor prognosis of breast cancer patients treated with taxane but a favorable prognosis with 5-fluoropyrimidines. And breast cancer cells with AGR3 high expression were resistant to taxane but sensitive to 5-fluoropyrimidines. CONCLUSION: AGR3 might be a potential prognostic indicator in luminal B subtype of IDC patients of histological grade I-II. And patients with AGR3 high expression should be treated with chemotherapy regimens consisting of 5-fluoropyrimidines but no taxane.
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spelling pubmed-69624922020-01-22 Anterior Gradient 3 Promotes Breast Cancer Development and Chemotherapy Response Xu, Qiao Shao, Ying Zhang, Jinman Zhang, Huikun Zhao, Yawen Liu, Xiaoli Guo, Zhifang Chong, Wei Gu, Feng Ma, Yongjie Cancer Res Treat Original Article PURPOSE: Anterior gradient 3 (AGR3) belongs to human anterior gradient (AGR) family. The function of AGR3 on cancer remains unknown. This research aimed to investigate if AGR3 had prognostic values in invasive ductal carcinoma (IDC) of breast cancer and could promote tumor progression. MATERIALS AND METHODS: AGR3 expression was detected in breast benign lesions, ductal carcinoma in situ and IDC by immunohistochemistry analysis. AGR3’s correlations with clinicopathological features and prognosis of IDC patients were analyzed. By cell function experiments, collagen gel droplet-embedded culture drug sensitivity test and cytotoxic analysis, AGR3’s impacts on proliferation, invasion ability, and chemotherapeutic drug sensitivity of breast cancer cells were also detected. RESULTS: AGR3 was up-regulated in luminal subtype of histological grade I-II of IDC patients and positively correlated with high risks of recurrence and distant metastasis. AGR3 high expression could lead to bone or liver metastasis and predict poor prognosis of luminal B. In cell lines, AGR3 could promote proliferation and invasion ability of breast cancer cells which were consistent with clinical analysis. Besides, AGR3 could indicate poor prognosis of breast cancer patients treated with taxane but a favorable prognosis with 5-fluoropyrimidines. And breast cancer cells with AGR3 high expression were resistant to taxane but sensitive to 5-fluoropyrimidines. CONCLUSION: AGR3 might be a potential prognostic indicator in luminal B subtype of IDC patients of histological grade I-II. And patients with AGR3 high expression should be treated with chemotherapy regimens consisting of 5-fluoropyrimidines but no taxane. Korean Cancer Association 2020-01 2019-07-08 /pmc/articles/PMC6962492/ /pubmed/31291711 http://dx.doi.org/10.4143/crt.2019.217 Text en Copyright © 2020 by the Korean Cancer Association This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Xu, Qiao
Shao, Ying
Zhang, Jinman
Zhang, Huikun
Zhao, Yawen
Liu, Xiaoli
Guo, Zhifang
Chong, Wei
Gu, Feng
Ma, Yongjie
Anterior Gradient 3 Promotes Breast Cancer Development and Chemotherapy Response
title Anterior Gradient 3 Promotes Breast Cancer Development and Chemotherapy Response
title_full Anterior Gradient 3 Promotes Breast Cancer Development and Chemotherapy Response
title_fullStr Anterior Gradient 3 Promotes Breast Cancer Development and Chemotherapy Response
title_full_unstemmed Anterior Gradient 3 Promotes Breast Cancer Development and Chemotherapy Response
title_short Anterior Gradient 3 Promotes Breast Cancer Development and Chemotherapy Response
title_sort anterior gradient 3 promotes breast cancer development and chemotherapy response
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962492/
https://www.ncbi.nlm.nih.gov/pubmed/31291711
http://dx.doi.org/10.4143/crt.2019.217
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