MDSCs在乳腺癌中的作用:转移、脂质代谢和治疗。

IF 4.7 2区 医学 Q2 CELL BIOLOGY
Ukjin Kim, Rumela Chakrabarti
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引用次数: 0

摘要

骨髓源性抑制细胞(MDSCs)是乳腺癌(BCa)免疫抑制微环境的主要贡献者之一。MDSCs在每个BCa转移部位都有独特的机制,脂质代谢是MDSCs发挥作用所必需的能量来源。此外,根据BCa亚型的不同,MDSCs表现出不同的特征。目前,对于针对乳腺癌亚型和转移部位的MDSCs还没有明确的认识。本文综述了BCa中发现的MDSCs的生物学和功能,重点介绍了转移和脂质代谢,并讨论了针对MDSCs的治疗方法。通过BCa亚型和转移生态位了解MDSC的特性和功能将是下一步细分BCa患者并提供定制治疗的先决条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MDSCs in breast cancer: metastasis, lipid metabolism, and therapeutics.

Myeloid-derived suppressor cells (MDSCs) are one of the major contributors to the immunosuppressive microenvironment of breast cancer (BCa). MDSCs have unique mechanisms for each BCa metastasis site, and lipid metabolism acts as an energy source necessary to perform the role of MDSCs. In addition, MDSCs show different characteristics depending on BCa subtype. Currently, there is no clear understanding of MDSCs tailored to subtypes and metastatic sites in breast cancer. Here, we reviewed the biology and function of MDSCs revealed in BCa, focusing on metastasis and lipid metabolism, and discussed treatments targeting MDSCs. Understanding MDSC properties and function by BCa subtype and metastatic niche will be a prerequisite for taking the next step in subdividing BCa patients and providing customized treatment.

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来源期刊
Molecular Cancer Research
Molecular Cancer Research 医学-细胞生物学
CiteScore
9.90
自引率
0.00%
发文量
280
审稿时长
4-8 weeks
期刊介绍: Molecular Cancer Research publishes articles describing novel basic cancer research discoveries of broad interest to the field. Studies must be of demonstrated significance, and the journal prioritizes analyses performed at the molecular and cellular level that reveal novel mechanistic insight into pathways and processes linked to cancer risk, development, and/or progression. Areas of emphasis include all cancer-associated pathways (including cell-cycle regulation; cell death; chromatin regulation; DNA damage and repair; gene and RNA regulation; genomics; oncogenes and tumor suppressors; signal transduction; and tumor microenvironment), in addition to studies describing new molecular mechanisms and interactions that support cancer phenotypes. For full consideration, primary research submissions must provide significant novel insight into existing pathway functions or address new hypotheses associated with cancer-relevant biologic questions.
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