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Lim1 癌基因作为转移性人肾透明细胞癌的一个新的治疗靶点。

The Lim1 oncogene as a new therapeutic target for metastatic human renal cell carcinoma.

机构信息

INSERM UMR_S1113, Section of Cell Signalisation and Communication in Kidney and Prostate Cancer, INSERM and University of Strasbourg, School of Medicine, Fédération de Médecine Translationnelle de Strasbourg (FMTS), 67085, Strasbourg, France.

Firalis, 68330, Huningue, France.

出版信息

Oncogene. 2019 Jan;38(1):60-72. doi: 10.1038/s41388-018-0413-y. Epub 2018 Aug 3.

Abstract

Metastatic clear cell renal cell carcinoma (CCC) remains incurable despite advances in the development of anti-angiogenic targeted therapies and the emergence of immune checkpoint inhibitors. We have previously shown that the sonic hedgehog-Gli signaling pathway is oncogenic in CCC allowing us to identify the developmental Lim1 transcription factor as a Gli target and as a new oncogene in CCC regulating cell proliferation and apoptosis, and promoting tumor growth. In this previous study, preliminary in vitro results also suggested that Lim1 may be implicated in metastatic spread. Here we investigated the potential pro-metastatic role of Lim1 in advanced CCC (1) in vitro using a panel of CCC cell lines expressing or not the von Hippel-Lindau (VHL) tumor suppressor gene either naturally or by gene transfer and (2) ex vivo in 30 CCC metastatic tissues, including lymph nodes, lung, skin, bone, and adrenal metastases, and (3) in vivo, using a metastatic model by intravenous injection of siRNA-transfected cells into Balb/c nude. Our in vitro results reveal that Lim1 knockdown time-dependently decreased CCC cell motility, migration, invasion, and clonogenicity by up to 50% regardless of their VHL status. Investigating the molecular machinery involved in these processes, we identified a large panel of Lim1 targets known to be involved in cell adhesion (paxillin and fibronectin), epithelial-mesenchymal transition (Twist1/2 and snail), invasion (MMP1/2/3/8/9), and metastatic progression (CXCR4, SDF-1, and ANG-1). Importantly, Lim1 was found constitutively expressed in all metastatic tissues. The H-score in metastatic tissues being significantly superior to the score in the corresponding primary tumor tissues (P value = 0.009). Furthermore, we showed that Lim1 silencing decreases pulmonary metastasis development in terms of number and size in the in vivo metastatic model of human CCC. Taken together, these experiments strengthen the potential therapeutic value of Lim1 targeting as a promising novel approach for treating metastatic human CCC.

摘要

转移性透明细胞肾细胞癌 (CCC) 尽管在抗血管生成靶向治疗的发展和免疫检查点抑制剂的出现方面取得了进展,但仍然无法治愈。我们之前已经表明,声波刺猬-Gli 信号通路在 CCC 中具有致癌性,这使我们能够将发育中的 Lim1 转录因子鉴定为 Gli 的靶标,以及 CCC 中的新致癌基因,调节细胞增殖和凋亡,并促进肿瘤生长。在之前的研究中,初步的体外结果还表明 Lim1 可能与转移扩散有关。在这里,我们研究了 Lim1 在高级 CCC 中的潜在促转移作用:(1) 在体外使用一组表达或不表达 von Hippel-Lindau (VHL) 肿瘤抑制基因的 CCC 细胞系,无论是自然表达还是通过基因转移;(2) 在 30 个 CCC 转移性组织中,包括淋巴结、肺、皮肤、骨骼和肾上腺转移,进行离体研究;(3) 使用静脉注射转染 siRNA 的细胞到 Balb/c 裸鼠中的转移模型进行体内研究。我们的体外结果表明,无论 VHL 状态如何,Lim1 敲低时间依赖性地降低了 CCC 细胞的运动性、迁移、侵袭和克隆形成能力,最高可达 50%。在研究涉及这些过程的分子机制时,我们鉴定了大量已知参与细胞黏附 (paxillin 和 fibronectin)、上皮-间充质转化 (Twist1/2 和 snail)、侵袭 (MMP1/2/3/8/9) 和转移进展 (CXCR4、SDF-1 和 ANG-1) 的 Lim1 靶标。重要的是,Lim1 在所有转移性组织中均呈组成性表达。在转移性组织中的 H 评分明显高于相应的原发性肿瘤组织中的评分 (P 值=0.009)。此外,我们还表明,在人 CCC 的体内转移模型中,Lim1 沉默可减少肺转移的发展,无论是转移数量还是大小。综上所述,这些实验加强了 Lim1 靶向治疗的潜在治疗价值,为治疗转移性人 CCC 提供了一种有前途的新方法。

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