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癌症相关间充质基质细胞的起源与产生:实体瘤的创新治疗靶点

The Origins and Generation of Cancer-Associated Mesenchymal Stromal Cells: An Innovative Therapeutic Target for Solid Tumors.

作者信息

Li Wei, Yang Jin, Zheng Ping, Li Haining, Zhao Shaolin

机构信息

Center of Research Laboratory, Department of Laboratory Medicine, The First People's Hospital of Lianyungang, Lianyungang, China.

Department of Clinical Laboratory Diagnostics, Kangda College of Nanjing Medical University, Lianyungang, China.

出版信息

Front Oncol. 2021 Aug 26;11:723707. doi: 10.3389/fonc.2021.723707. eCollection 2021.

Abstract

Cancer-associated mesenchymal stromal cells (CA-MSCs) have been isolated from various types of tumors and are characterized by their vigorous pro-tumorigenic functions. However, very little is known about the origins and generating process of CA-MSCs, which may facilitate the identification of biomarkers for diagnosis or innovative targets for anti-cancer therapy to restrain the tumor growth, spread and chemotherapy resistance. Current evidences have indicated that both distally recruited and local resident MSCs are the primary origins of CA-MSCs. In a tissue type-dependent mode, tumor cells together with the TME components prompt the malignant transition of tumor "naïve" MSCs into CA-MSCs in a direct cell-to-cell contact, paracrine or exosome-mediated manner. In this review, we discuss the transition of phenotypes and functions of naïve MSCs into CA-MSCs influenced by tumor cells or non-tumor cells in the TME. The key areas remaining poorly understood are also highlighted and concluded herein.

摘要

癌症相关间充质基质细胞(CA-MSCs)已从多种类型的肿瘤中分离出来,其特征在于具有强大的促肿瘤功能。然而,人们对CA-MSCs的起源和生成过程知之甚少,而这可能有助于识别用于诊断的生物标志物或用于抗癌治疗的创新靶点,以抑制肿瘤生长、扩散和化疗耐药性。目前的证据表明,远端募集的和局部驻留的间充质干细胞都是CA-MSCs的主要来源。在组织类型依赖模式下,肿瘤细胞与肿瘤微环境(TME)成分一起,以直接的细胞间接触、旁分泌或外泌体介导的方式促使肿瘤“未成熟”间充质干细胞向CA-MSCs发生恶性转变。在这篇综述中,我们讨论了在TME中受肿瘤细胞或非肿瘤细胞影响的未成熟间充质干细胞向CA-MSCs的表型和功能转变。本文还突出并总结了仍了解不足的关键领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44c8/8427299/5e04e6d8f4c6/fonc-11-723707-g001.jpg

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