BPIFB1 promotes metastasis of hormone receptor‐positive breast cancer via inducing macrophage M2‐like polarization

Author:

Hu Anbang1,Liu Yansong1,Zhang Hanyu1,Wang Ting1,Zhang Jiarui1,Cheng Weilun1,Yu Tianshui1,Duan Yunqiang1,Feng Jianyuan1,Chen Ziang1,Ding Yu2,Li Yanling1,Li Mingcui1,Rong Zhiyuan1,Shang Yuhang1,Shakila Suborna S.1,Zou Yiyun1,Ma Fei1,Guo Baoliang1ORCID

Affiliation:

1. Department of General Surgery The Second Affiliated Hospital of Harbin Medical University Harbin China

2. Department of General Surgery Daqing Oilfield General Hospital Daqing China

Abstract

AbstractMetastasis is an important factor affecting the prognosis of hormone receptor‐positive breast cancer (BC). However, the molecular basis for migration and invasion of tumor cells remains poorly understood. Here, we identify that bactericidal/permeability‐increasing‐fold‐containing family B member 1 (BPIFB1), which plays an important role in innate immunity, is significantly elevated in breast cancer and associated with lymph node metastasis. High expression of BPIFB1 and its coding mRNA are significantly associated with poor prognosis of hormone receptor‐positive BC. Using enrichment analysis and constructing immune infiltration evaluation, we predict the potential ability of BPIFB1 to promote macrophage M2 polarization. Finally, we demonstrate that BPIFB1 promotes the metastasis of hormone receptor‐positive BC by stimulating the M2‐like polarization of macrophages via the establishment of BC tumor cells/THP1 co‐culture system, qPCR, Transwell assay, and animal experiments. To our knowledge, this is the first report on the role of BPIFB1 as a tumor promoter by activating the macrophage M2 polarization in hormone receptor‐positive breast carcinoma. Together, these results provide novel insights into the mechanism of BPIFB1 in BC.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cancer Research,Oncology,General Medicine

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