Paclitaxel Promotes Tumor-Infiltrating Macrophages in Breast Cancer

Objective: Breast cancer remains the most threatening triggers of cancer death in women. Drug resistance inevitably leads to the weakness of treatment for breast cancer. Macrophages, as one of the most abundant immune cells in tumor immune-infiltrating microenvironment, involves in cell survival, mi...

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Main Authors: Jun Shen MD, Cong Chen MD, Zhaoqing Li MD, Shufang Hu MD
Format: Article
Language:English
Published: SAGE Publishing 2020-08-01
Series:Technology in Cancer Research & Treatment
Online Access:https://doi.org/10.1177/1533033820945821
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spelling doaj-1c2fc4611a4845838fa91a030f3c5f302020-11-25T03:46:29ZengSAGE PublishingTechnology in Cancer Research & Treatment1533-03382020-08-011910.1177/1533033820945821Paclitaxel Promotes Tumor-Infiltrating Macrophages in Breast CancerJun Shen MD0Cong Chen MD1Zhaoqing Li MD2Shufang Hu MD3 Department of Surgical Oncology, , Hangzhou, Zhejiang Province, China Biomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province, Hangzhou, Zhejiang Province, China Department of Surgical Oncology, , Hangzhou, Zhejiang Province, China Department of Breast Surgery, , Hangzhou, Zhejiang Province, ChinaObjective: Breast cancer remains the most threatening triggers of cancer death in women. Drug resistance inevitably leads to the weakness of treatment for breast cancer. Macrophages, as one of the most abundant immune cells in tumor immune-infiltrating microenvironment, involves in cell survival, migration, and invasion of breast cancer. Methods: In this study, we compared the proportions of macrophages in patients with breast cancer with and without paclitaxel treatment, and investigated the targeted genes associated with macrophages for paclitaxel response. To explore the relationship between drug-related genes and breast cancer prognosis, survival analysis based on the drug-related genes were performed by website of Kaplan-Meier plotter with the threshold of significant P value < .05. Results: Compared to the normal samples, we revealed that paclitaxel significantly enhanced the ratio of macrophages in the tumor microenvironment. Furthermore, the expression of 3 drug-related genes (IFT46, PEX11A, and TMEM223) were significantly negatively associated with the proportions of macrophages. And it is worth to notice that PEX11A and TMEM223 were associated with better progression-free survival outcomes of patients with breast cancer. Moreover, PEX11A was associated with longer overall survival time of breast cancer. Conclusion: Taken all together, all the findings support to gain a better understanding to the development of more effective therapies targeted with paclitaxel.https://doi.org/10.1177/1533033820945821
collection DOAJ
language English
format Article
sources DOAJ
author Jun Shen MD
Cong Chen MD
Zhaoqing Li MD
Shufang Hu MD
spellingShingle Jun Shen MD
Cong Chen MD
Zhaoqing Li MD
Shufang Hu MD
Paclitaxel Promotes Tumor-Infiltrating Macrophages in Breast Cancer
Technology in Cancer Research & Treatment
author_facet Jun Shen MD
Cong Chen MD
Zhaoqing Li MD
Shufang Hu MD
author_sort Jun Shen MD
title Paclitaxel Promotes Tumor-Infiltrating Macrophages in Breast Cancer
title_short Paclitaxel Promotes Tumor-Infiltrating Macrophages in Breast Cancer
title_full Paclitaxel Promotes Tumor-Infiltrating Macrophages in Breast Cancer
title_fullStr Paclitaxel Promotes Tumor-Infiltrating Macrophages in Breast Cancer
title_full_unstemmed Paclitaxel Promotes Tumor-Infiltrating Macrophages in Breast Cancer
title_sort paclitaxel promotes tumor-infiltrating macrophages in breast cancer
publisher SAGE Publishing
series Technology in Cancer Research & Treatment
issn 1533-0338
publishDate 2020-08-01
description Objective: Breast cancer remains the most threatening triggers of cancer death in women. Drug resistance inevitably leads to the weakness of treatment for breast cancer. Macrophages, as one of the most abundant immune cells in tumor immune-infiltrating microenvironment, involves in cell survival, migration, and invasion of breast cancer. Methods: In this study, we compared the proportions of macrophages in patients with breast cancer with and without paclitaxel treatment, and investigated the targeted genes associated with macrophages for paclitaxel response. To explore the relationship between drug-related genes and breast cancer prognosis, survival analysis based on the drug-related genes were performed by website of Kaplan-Meier plotter with the threshold of significant P value < .05. Results: Compared to the normal samples, we revealed that paclitaxel significantly enhanced the ratio of macrophages in the tumor microenvironment. Furthermore, the expression of 3 drug-related genes (IFT46, PEX11A, and TMEM223) were significantly negatively associated with the proportions of macrophages. And it is worth to notice that PEX11A and TMEM223 were associated with better progression-free survival outcomes of patients with breast cancer. Moreover, PEX11A was associated with longer overall survival time of breast cancer. Conclusion: Taken all together, all the findings support to gain a better understanding to the development of more effective therapies targeted with paclitaxel.
url https://doi.org/10.1177/1533033820945821
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