特异性蛋白1启动循环肿瘤细胞上皮-间质转化,抑制前列腺癌转移。

IF 5.3 2区 医学 Q1 ONCOLOGY
Mei Yang, Lin Jie Li, Guo Ping Qiu, Hui Liu, Fei Gao
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引用次数: 0

摘要

循环肿瘤细胞(CTCs)作为肿瘤转移的种子,在肿瘤的诊断、预后和治疗方面具有很大的前景。根据生物标志物的表达,ctc可分为上皮(E)、间充质(M)或杂交(M/E)表型。目前,CTC表型在转移性前列腺癌(PCa)中的作用尚不清楚。在目前的研究中,使用Canpatrol™技术从102例PCa患者中分离出ctc。采用荧光原位杂交技术(FISH)对ctc进行分类。利用生物信息学软件对EMT调控因子进行分析。慢病毒转染PC3细胞后,特异性蛋白1 (SP1)过表达。Transwell法测定体外细胞侵袭情况。采用小鼠转移模型,评价过表达sp1的PC3细胞经尾静脉注射后的播种能力。研究发现,转移性PCa中总CTCs (T-CTCs)、E-CTCs和混合CTCs的细胞计数明显高于局部PCa。T-CTC计数(bbb14)被确定为转移的独立危险因素,预测转移性PCa的敏感性为90.48%,特异性为96.67%。SP1被生物信息学鉴定为有价值的EMT调节因子。SP1在PC3细胞中过表达可诱导EMT,增强细胞侵袭,但在体内可抑制肺转移。总之,T-CTC计数预测转移性前列腺癌。PCa ctc向M表型的极化降低了它们启动转移的能力。SP1过表达诱导EMT并抑制PCa ctc的转移定植。因此,通过SP1增强在ctc中诱导EMT可能有望作为一种新的治疗PCa的方法,通过延缓转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Specificity protein 1 initiates epithelial-mesenchymal transition of circulating tumor cells to inhibit metastasis in prostate cancer.

Circulating tumor cells (CTCs), as seeds for metastasis, hold great promise for cancer diagnosis, prognosis, and treatment. Based on the expression of biomarkers, CTCs can be categorized as epithelial (E), mesenchymal (M), or hybrid (M/E) phenotypes. At present, the role of CTC phenotypes in metastatic prostate cancer (PCa) is not clear. In the current study, CTCs were isolated from 102 PCa patients using the Canpatrol™ technology. Fluorescence in situ hybridization (FISH) was used to categorize CTCs. The EMT regulators were analyzed by bioinformatics software. Specificity protein 1 (SP1) was overexpressed in PC3 cells by lentiviral transfection. Transwell assay was used to assess cell invasion in vitro. A mouse model of metastasis was used to evaluate the seeding capability of SP1-overexpressing PC3 cells administered via tail vein injection. It was found that the cell counts of total CTCs (T-CTCs), E-CTCs, and hybrid-CTCs were significantly higher in metastatic PCa than local PCa. T-CTC count (> 14) was identified as an independent risk factor for metastasis, predicting metastatic PCa with a sensitivity of 90.48% and a specificity of 96.67%. SP1 was identified as a valuable EMT regulator by bioinformatics. SP1 overexpression in PC3 cells induced EMT and enhanced cell invasion in vitro, however, it inhibited lung metastasis in vivo. In conclusion, the T-CTC count predicted metastatic PCa. Polarization of PCa CTCs toward the M phenotype reduced their metastasis-initiating capability. SP1 overexpression induced EMT and repressed metastatic colonization of PCa CTCs. Thus, the induction of EMT in CTCs by SP1 augmentation may hold promise as a novel treatment for PCa by staving off metastasis.

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来源期刊
CiteScore
10.90
自引率
1.70%
发文量
360
审稿时长
1 months
期刊介绍: Cancer Cell International publishes articles on all aspects of cancer cell biology, originating largely from, but not limited to, work using cell culture techniques. The journal focuses on novel cancer studies reporting data from biological experiments performed on cells grown in vitro, in two- or three-dimensional systems, and/or in vivo (animal experiments). These types of experiments have provided crucial data in many fields, from cell proliferation and transformation, to epithelial-mesenchymal interaction, to apoptosis, and host immune response to tumors. Cancer Cell International also considers articles that focus on novel technologies or novel pathways in molecular analysis and on epidemiological studies that may affect patient care, as well as articles reporting translational cancer research studies where in vitro discoveries are bridged to the clinic. As such, the journal is interested in laboratory and animal studies reporting on novel biomarkers of tumor progression and response to therapy and on their applicability to human cancers.
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