Expression of ICOSL is associated with decreased survival in invasive breast cancer

Background Inducible co-stimulator (ICOS) is a CD28-related molecule exclusively expressed on activated T cells and plays a critical role in modulating the immune response in breast cancer. The blockage of ICOS pathway has been shown to inhibit the activity of Type 2 T helper cells, thus potentially...

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Main Authors: Bin Wang, Huayong Jiang, Tingyang Zhou, Ning Ma, Wei Liu, Yajie Wang, Li Zuo
Format: Article
Language:English
Published: PeerJ Inc. 2019-05-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/6903.pdf
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author Bin Wang
Huayong Jiang
Tingyang Zhou
Ning Ma
Wei Liu
Yajie Wang
Li Zuo
author_facet Bin Wang
Huayong Jiang
Tingyang Zhou
Ning Ma
Wei Liu
Yajie Wang
Li Zuo
author_sort Bin Wang
collection DOAJ
description Background Inducible co-stimulator (ICOS) is a CD28-related molecule exclusively expressed on activated T cells and plays a critical role in modulating the immune response in breast cancer. The blockage of ICOS pathway has been shown to inhibit the activity of Type 2 T helper cells, thus potentially protecting against cancer growth. The current study aims to investigate the correlation between inducible co-stimulator ligand (ICOSL) expression in tumor tissues and the prognoses of patients with invasive breast cancer. Methods Tumor samples from 562 Chinese patients with invasive breast carcinomas were collected between 2003 and 2010. The expression of ICOSL on breast tumor and adjacent non-cancerous tissue was determined via immunohistochemistry. The overall survival (OS) of patients with positive and negative ICOSL expression were described using Kaplan–Meier curves, respectively. Parametric correlation method was used to analyze the correlation between ICOSL expression and other clinicopathological parameters. ICOSL was selected as a dependent variable for multivariate analysis. Results Positive ICOSL expression was identified on the plasma membrane in both cytoplasm and the nucleus of breast cancer cells. Membrane-expressed ICOSL is determined as an independent prognostic factor for OS in breast cancer but without significantly correlating with other clinicopathologic parameters such as age, menopausal status, depth of invasion, lymph node metastasis status, histologic classification, etc. Conclusion Our study suggests that the up-regulated expression of ICOSL protein in breast tumor cells can be associated with poor prognoses in invasive breast carcinomas.
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spelling doaj.art-6a9473e958014de08c78086cc0baac9c2023-12-03T00:47:16ZengPeerJ Inc.PeerJ2167-83592019-05-017e690310.7717/peerj.6903Expression of ICOSL is associated with decreased survival in invasive breast cancerBin Wang0Huayong Jiang1Tingyang Zhou2Ning Ma3Wei Liu4Yajie Wang5Li Zuo6Department of Oncology, Changhai Hospital, the Second Military Medical University, Shanghai, ChinaDepartment of Radiation Oncology, The 7th Medical Center of PLA General Hospital, Beijing, ChinaRadiologic Sciences and Respiratory Therapy Division, School of Health and Rehabilitation Sciences, The Ohio State University College of Medicine, Columbus, OH, USAClinical Laboratory, 905th Hospital of PLA, Shanghai, ChinaDepartment of Radiation Oncology, Mayo Clinic Arizona, Pheonix, AZ, USADepartment of Oncology, Changhai Hospital, the Second Military Medical University, Shanghai, ChinaRadiologic Sciences and Respiratory Therapy Division, School of Health and Rehabilitation Sciences, The Ohio State University College of Medicine, Columbus, OH, USABackground Inducible co-stimulator (ICOS) is a CD28-related molecule exclusively expressed on activated T cells and plays a critical role in modulating the immune response in breast cancer. The blockage of ICOS pathway has been shown to inhibit the activity of Type 2 T helper cells, thus potentially protecting against cancer growth. The current study aims to investigate the correlation between inducible co-stimulator ligand (ICOSL) expression in tumor tissues and the prognoses of patients with invasive breast cancer. Methods Tumor samples from 562 Chinese patients with invasive breast carcinomas were collected between 2003 and 2010. The expression of ICOSL on breast tumor and adjacent non-cancerous tissue was determined via immunohistochemistry. The overall survival (OS) of patients with positive and negative ICOSL expression were described using Kaplan–Meier curves, respectively. Parametric correlation method was used to analyze the correlation between ICOSL expression and other clinicopathological parameters. ICOSL was selected as a dependent variable for multivariate analysis. Results Positive ICOSL expression was identified on the plasma membrane in both cytoplasm and the nucleus of breast cancer cells. Membrane-expressed ICOSL is determined as an independent prognostic factor for OS in breast cancer but without significantly correlating with other clinicopathologic parameters such as age, menopausal status, depth of invasion, lymph node metastasis status, histologic classification, etc. Conclusion Our study suggests that the up-regulated expression of ICOSL protein in breast tumor cells can be associated with poor prognoses in invasive breast carcinomas.https://peerj.com/articles/6903.pdfICOSLPrognosisInvasive breast cancer
spellingShingle Bin Wang
Huayong Jiang
Tingyang Zhou
Ning Ma
Wei Liu
Yajie Wang
Li Zuo
Expression of ICOSL is associated with decreased survival in invasive breast cancer
PeerJ
ICOSL
Prognosis
Invasive breast cancer
title Expression of ICOSL is associated with decreased survival in invasive breast cancer
title_full Expression of ICOSL is associated with decreased survival in invasive breast cancer
title_fullStr Expression of ICOSL is associated with decreased survival in invasive breast cancer
title_full_unstemmed Expression of ICOSL is associated with decreased survival in invasive breast cancer
title_short Expression of ICOSL is associated with decreased survival in invasive breast cancer
title_sort expression of icosl is associated with decreased survival in invasive breast cancer
topic ICOSL
Prognosis
Invasive breast cancer
url https://peerj.com/articles/6903.pdf
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