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Endoplasmic reticulum stress induces secretion of high-mobility group proteins and is associated with tumor-infiltrating lymphocytes in triple-negative breast cancer

BACKGROUND: Although the prognostic and predictive significance of tumor-infiltrating lymphocytes (TILs) in triple-negative breast cancer (TNBC) have been shown, the cause of the TIL influx is unclear. Here, we investigated whether extracellular secretion of HMGN1 is associated with TIL influx, as w...

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Autores principales: Park, In Ah, Heo, Sun-Hee, Song, In Hye, Kim, Young-Ae, Park, Hye Seon, Bang, Won Seon, Park, Suk Young, Jo, Jeong-Hyon, Lee, Hee Jin, Gong, Gyungyub
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312361/
https://www.ncbi.nlm.nih.gov/pubmed/27494867
http://dx.doi.org/10.18632/oncotarget.11010
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author Park, In Ah
Heo, Sun-Hee
Song, In Hye
Kim, Young-Ae
Park, Hye Seon
Bang, Won Seon
Park, Suk Young
Jo, Jeong-Hyon
Lee, Hee Jin
Gong, Gyungyub
author_facet Park, In Ah
Heo, Sun-Hee
Song, In Hye
Kim, Young-Ae
Park, Hye Seon
Bang, Won Seon
Park, Suk Young
Jo, Jeong-Hyon
Lee, Hee Jin
Gong, Gyungyub
author_sort Park, In Ah
collection PubMed
description BACKGROUND: Although the prognostic and predictive significance of tumor-infiltrating lymphocytes (TILs) in triple-negative breast cancer (TNBC) have been shown, the cause of the TIL influx is unclear. Here, we investigated whether extracellular secretion of HMGN1 is associated with TIL influx, as well as increased endoplasmic reticulum stress (ERS), in human TNBC. METHODS: We reviewed the slides of 767 patients with TNBC and evaluated the TIL levels. We also assessed the expression of HMGs and several ERS-associated molecules using immunohistochemical staining. Western blot analysis of human TNBC cell lines and pharmacological ERS inducers was used to determine if HMGN1 migrates from the nucleus to the extracellular space in response to ERS. RESULTS: On immunohistochemical staining, either higher nuclear or cytoplasmic expression of both HMGB1 and HMGN1 was significantly associated with ERS. TILs showed a positive correlation with the cytoplasmic expression of the HMGs. Western blot analysis of TNBC cell lines showed that ERS induction resulted in the secretion of HMG proteins. CONCLUSIONS: This is the first study to elucidate the associations among ERS, secretion of HMGs, and degree of TILs in TNBCs. Understanding the mechanisms of TIL influx will help in the development of effective immunotherapeutic agents for TNBC.
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spelling pubmed-53123612017-03-06 Endoplasmic reticulum stress induces secretion of high-mobility group proteins and is associated with tumor-infiltrating lymphocytes in triple-negative breast cancer Park, In Ah Heo, Sun-Hee Song, In Hye Kim, Young-Ae Park, Hye Seon Bang, Won Seon Park, Suk Young Jo, Jeong-Hyon Lee, Hee Jin Gong, Gyungyub Oncotarget Research Paper BACKGROUND: Although the prognostic and predictive significance of tumor-infiltrating lymphocytes (TILs) in triple-negative breast cancer (TNBC) have been shown, the cause of the TIL influx is unclear. Here, we investigated whether extracellular secretion of HMGN1 is associated with TIL influx, as well as increased endoplasmic reticulum stress (ERS), in human TNBC. METHODS: We reviewed the slides of 767 patients with TNBC and evaluated the TIL levels. We also assessed the expression of HMGs and several ERS-associated molecules using immunohistochemical staining. Western blot analysis of human TNBC cell lines and pharmacological ERS inducers was used to determine if HMGN1 migrates from the nucleus to the extracellular space in response to ERS. RESULTS: On immunohistochemical staining, either higher nuclear or cytoplasmic expression of both HMGB1 and HMGN1 was significantly associated with ERS. TILs showed a positive correlation with the cytoplasmic expression of the HMGs. Western blot analysis of TNBC cell lines showed that ERS induction resulted in the secretion of HMG proteins. CONCLUSIONS: This is the first study to elucidate the associations among ERS, secretion of HMGs, and degree of TILs in TNBCs. Understanding the mechanisms of TIL influx will help in the development of effective immunotherapeutic agents for TNBC. Impact Journals LLC 2016-08-02 /pmc/articles/PMC5312361/ /pubmed/27494867 http://dx.doi.org/10.18632/oncotarget.11010 Text en Copyright: © 2016 Park et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Park, In Ah
Heo, Sun-Hee
Song, In Hye
Kim, Young-Ae
Park, Hye Seon
Bang, Won Seon
Park, Suk Young
Jo, Jeong-Hyon
Lee, Hee Jin
Gong, Gyungyub
Endoplasmic reticulum stress induces secretion of high-mobility group proteins and is associated with tumor-infiltrating lymphocytes in triple-negative breast cancer
title Endoplasmic reticulum stress induces secretion of high-mobility group proteins and is associated with tumor-infiltrating lymphocytes in triple-negative breast cancer
title_full Endoplasmic reticulum stress induces secretion of high-mobility group proteins and is associated with tumor-infiltrating lymphocytes in triple-negative breast cancer
title_fullStr Endoplasmic reticulum stress induces secretion of high-mobility group proteins and is associated with tumor-infiltrating lymphocytes in triple-negative breast cancer
title_full_unstemmed Endoplasmic reticulum stress induces secretion of high-mobility group proteins and is associated with tumor-infiltrating lymphocytes in triple-negative breast cancer
title_short Endoplasmic reticulum stress induces secretion of high-mobility group proteins and is associated with tumor-infiltrating lymphocytes in triple-negative breast cancer
title_sort endoplasmic reticulum stress induces secretion of high-mobility group proteins and is associated with tumor-infiltrating lymphocytes in triple-negative breast cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312361/
https://www.ncbi.nlm.nih.gov/pubmed/27494867
http://dx.doi.org/10.18632/oncotarget.11010
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