CSF2通过FAK信号通路上调脂肪细胞中CXCL3的表达,促进乳腺癌转移。

IF 5.3 2区 生物学 Q2 CELL BIOLOGY
Xi He, Lieliang Wang, Honghui Li, Yaru Liu, Chang Tong, Caifeng Xie, Xiaohua Yan, Daya Luo, Xiangyang Xiong
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引用次数: 0

摘要

最近的研究表明,肿瘤微环境中的癌症相关脂肪细胞(CAAs)参与了乳腺癌的恶性进展。然而,CAA形成的潜在机制及其对乳腺癌发展的影响尚不清楚。在这里,我们发现CSF2在CAAs和乳腺癌细胞中都高度表达。CSF2通过Stat3信号通路促进脂肪细胞的炎症表型改变,导致多种细胞因子和蛋白酶的分泌,尤其是C-X-C基序趋化因子配体3 (CXCL3)。脂肪细胞衍生的CXCL3在乳腺癌细胞上与其特异性受体CXCR2结合,激活FAK通路,增强乳腺癌细胞的间充质表型、迁移和侵袭。此外,针对CSF2和CXCR2的联合治疗在体内对脂肪细胞诱导的小鼠4T1细胞肺转移有协同抑制作用。这些发现阐明了一种新的乳腺癌转移机制,并为乳腺癌转移提供了潜在的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CSF2 upregulates CXCL3 expression in adipocytes to promote metastasis of breast cancer via the FAK signaling pathway.

Recent studies have demonstrated that cancer-associated adipocytes (CAAs) in the tumor microenvironment are involved in the malignant progression of breast cancer. However, the underlying mechanism of CAA formation and its effects on the development of breast cancer are still unknown. Here, we show that CSF2 is highly expressed in both CAAs and breast cancer cells. CSF2 promotes inflammatory phenotypic changes of adipocytes through the Stat3 signaling pathway, leading to the secretion of multiple cytokines and proteases, particularly C-X-C motif chemokine ligand 3 (CXCL3). Adipocyte-derived CXCL3 binds to its specific receptor CXCR2 on breast cancer cells and activates the FAK pathway, enhancing the mesenchymal phenotype, migration, and invasion of breast cancer cells. In addition, a combination treatment targeting CSF2 and CXCR2 shows a synergistic inhibitory effect on adipocyte-induced lung metastasis of mouse 4T1 cells in vivo. These findings elucidate a novel mechanism of breast cancer metastasis and provide a potential therapeutic strategy for breast cancer metastasis.

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来源期刊
CiteScore
9.60
自引率
1.80%
发文量
1383
期刊介绍: The Journal of Molecular Cell Biology ( JMCB ) is a full open access, peer-reviewed online journal interested in inter-disciplinary studies at the cross-sections between molecular and cell biology as well as other disciplines of life sciences. The broad scope of JMCB reflects the merging of these life science disciplines such as stem cell research, signaling, genetics, epigenetics, genomics, development, immunology, cancer biology, molecular pathogenesis, neuroscience, and systems biology. The journal will publish primary research papers with findings of unusual significance and broad scientific interest. Review articles, letters and commentary on timely issues are also welcome. JMCB features an outstanding Editorial Board, which will serve as scientific advisors to the journal and provide strategic guidance for the development of the journal. By selecting only the best papers for publication, JMCB will provide a first rate publishing forum for scientists all over the world.
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