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癌相关成纤维细胞衍生的TIAM1通过调控ZEB2促进口腔鳞状细胞癌细胞生长和转移。

CAFs-derived TIAM1 Promotes OSCC Cell Growth and Metastasis by Regulating ZEB2.

作者信息

Yao Yao, Lv Ruya, Dong Jingjing, Chen Qi'an

机构信息

Department of stomatology, Jingzhou Central Hospital, Jingzhou City, Hubei Province, China.

Department of stomatology, Jingzhou Hospital Affiliated to Yangtze University, Jingzhou City, Hubei Province, China.

出版信息

Cell Biochem Biophys. 2025 Mar;83(1):729-740. doi: 10.1007/s12013-024-01505-4. Epub 2024 Sep 10.

Abstract

Previous studies have suggested that cancer-associated fibroblasts (CAFs) within the tumor microenvironment are a critical factor in tumorigenesis and tumor development. However, the regulatory mechanisms of CAFs on oral squamous cell carcinoma (OSCC) are poorly defined. A CAF-conditioned medium (CAF-CM) was collected and applied to culture OSCC cells. Then, cell viability, proliferation, migration, and invasion were evaluated using 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT), 5-ethynyl-2'-deoxyuridine (EdU), Transwell, and scratch healing assays. T-Lymphoma Invasion and Metastasis 1 (TIAM1), zinc finger E-box-binding homeobox 2 (ZEB2), E-cadherin, and increased N-cadherin protein levels were determined using western blot. TIAM1 and ZEB2 mRNA levels were measured using real-time quantitative polymerase chain reaction (RT-qPCR). Their interaction was analyzed using Co-immunoprecipitation (Co-IP) assay. SCC25 cells with or without (TIAM1-silencing) CAFs were subcutaneously inoculated in nude mice to assess the effect of TIAM1 in CAFs on OSCC tumor growth in vivo. CAFs expedited OSCC cell proliferation, migration, invasion, and EMT. TIAM1 and ZEB2 expression were upregulated in OSCC patients and OSCC cells, and the TIAM1 level was much higher in CAFs than in OSCC cells. Furthermore, TIAM1 knockdown in CAFs might partly abolish the promotion of CAFs on OSCC cell development, implying that TIAM1 might be secreted by CAFs into the culture medium to exert its effects inside OSCCs. TIAM1 might increase ZEB2 expression, and ZEB2 upregulation might partly reverse the repression of TIAM1 silencing in CAFs on OSCC cell malignant behaviors. In vivo studies confirmed that CAFs accelerated OSCC tumor growth, these effects were partially counteracted by TIAM1 downregulation. Overall, TIAM1 secreted by CAFs could expedite OSCC cell growth and metastasis by regulating ZEB2, providing a promising therapeutic target for OSCC treatment.

摘要

先前的研究表明,肿瘤微环境中的癌症相关成纤维细胞(CAFs)是肿瘤发生和发展的关键因素。然而,CAFs对口腔鳞状细胞癌(OSCC)的调控机制尚不清楚。收集CAF条件培养基(CAF-CM)并用于培养OSCC细胞。然后,使用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2-H-四氮唑溴盐(MTT)、5-乙炔基-2'-脱氧尿苷(EdU)、Transwell和划痕愈合试验评估细胞活力、增殖、迁移和侵袭。使用蛋白质印迹法测定T淋巴瘤侵袭和转移1(TIAM1)、锌指E盒结合同源框2(ZEB2)、E-钙黏蛋白和N-钙黏蛋白蛋白水平的升高。使用实时定量聚合酶链反应(RT-qPCR)测量TIAM1和ZEB2 mRNA水平。使用免疫共沉淀(Co-IP)试验分析它们的相互作用。将有或没有(TIAM1沉默)CAFs的SCC25细胞皮下接种到裸鼠中,以评估CAFs中的TIAM1对体内OSCC肿瘤生长的影响。CAFs促进了OSCC细胞的增殖迁移、侵袭和上皮-间质转化(EMT)。TIAM1和ZEB2在OSCC患者和OSCC细胞中的表达上调,并且CAFs中的TIAM1水平远高于OSCC细胞。此外,CAFs中TIAM1的敲低可能部分消除CAFs对OSCC细胞发育的促进作用,这意味着TIAM1可能由CAFs分泌到培养基中以在OSCC内部发挥其作用。TIAM1可能增加ZEB2的表达,并且ZEB2的上调可能部分逆转CAFs中TIAM1沉默对OSCC细胞恶性行为的抑制作用。体内研究证实,CAFs加速了OSCC肿瘤的生长,TIAM1的下调部分抵消了这些作用。总体而言,CAFs分泌的TIAM1可通过调节ZEB2来加速OSCC细胞的生长和转移,为OSCC治疗提供了一个有前景的治疗靶点。

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