JUNB suppresses distant metastasis by influencing the initial metastatic stage
Autor: | Peter Angel, Juliane Wutschka, Sila Appak-Baskoy, Bettina Kast, Marina Schorpp-Kistner, Hans-Peter Sinn, Melanie Sator-Schmitt, Jochen Hess |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Cancer Research Stromal cell Angiogenesis JUNB Breast Neoplasms Mice Transgenic Metastasis Mice 03 medical and health sciences 0302 clinical medicine hemic and lymphatic diseases Animals Humans Medicine Neoplasm Invasiveness Neoplasm Metastasis Tumor microenvironment business.industry Cancer General Medicine medicine.disease Primary tumor 030104 developmental biology Oncology 030220 oncology & carcinogenesis Cancer cell Cancer research Female Transcription factor business Research Paper Transcription Factors |
Zdroj: | Clinical & Experimental Metastasis |
ISSN: | 1573-7276 0262-0898 |
DOI: | 10.1007/s10585-021-10108-9 |
Popis: | The complex interactions between cells of the tumor microenvironment and cancer cells are considered a major determinant of cancer progression and metastasis. Yet, our understanding of the mechanisms of metastatic disease is not sufficient to successfully treat patients with advanced-stage cancer. JUNB is a member of the AP-1 transcription factor family shown to be frequently deregulated in human cancer and associated with invasion and metastasis. A strikingly high stromal JUNB expression in human breast cancer samples prompted us to functionally investigate the consequences of JUNB loss in cells of the tumor microenvironment on cancer progression and metastasis in mice. To adequately mimic the clinical situation, we applied a syngeneic spontaneous breast cancer metastasis model followed by primary tumor resection and identified stromal JUNB as a potent suppressor of distant metastasis. Comprehensive characterization of the JUNB-deficient tumor microenvironment revealed a strong influx of myeloid cells into primary breast tumors and lungs at early metastatic stage. In these infiltrating neutrophils, BV8 and MMP9, proteins promoting angiogenesis and tissue remodeling, were specifically upregulated in a JUNB-dependent manner. Taken together, we established stromal JUNB as a strong suppressor of distant metastasis. Consequently, therapeutic strategies targeting AP-1 should be carefully designed not to interfere with stromal JUNB expression as this may be detrimental for cancer patients. Supplementary Information The online version contains supplementary material available at 10.1007/s10585-021-10108-9. |
Databáze: | OpenAIRE |
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