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整合素α5触发肾细胞癌的转移潜能。

Integrin α5 triggers the metastatic potential in renal cell carcinoma.

作者信息

Breuksch Ines, Prosinger Franz, Baehr Fabian, Engelhardt Franz-Peter, Bauer Heide-Katharina, Thüroff Joachim W, Heimes Anne-Sophie, Hasenburg Annette, Prawitt Dirk, Brenner Walburgis

机构信息

Department of Gynecology, Johannes Gutenberg University Medical Center, 55131 Mainz, Germany.

Department of Urology, Johannes Gutenberg University Medical Center, 55131 Mainz, Germany.

出版信息

Oncotarget. 2017 Nov 18;8(64):107530-107542. doi: 10.18632/oncotarget.22501. eCollection 2017 Dec 8.

DOI:10.18632/oncotarget.22501
PMID:29296184
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5746086/
Abstract

The therapy of advanced renal cell carcinoma (RCC) is still a major challenge. To intervene therapeutically a deeper comprehension of the particular steps of metastasis is necessary. In this context membrane bound receptors like integrins play a decisive role. We analyzed the integrin α5 expression in 141 clear cell RCC patients by Western blot. Patients with RCC expressed a significant higher level of integrin α5 in tumor than in normal tissue. The integrin α5 expression correlated with tumor grade, the development of distant metastases within five years after tumor nephrectomy and reduced survival. The RCC cell lines Caki-1 and CCF-RC1, which highly express integrin α5, were treated with fibronectin in combination with or without an inhibiting anti-integrin α5 antibody. Afterwards the migration, adhesion, viability and prominent signaling molecules were analyzed. Both cell lines showed a significant reduced migration potential as well as a decreased adhesion potential to fibronectin after treatment with an integrin α5 blocking antibody. A contribution of the AKT and ERK1/2 signaling pathways could be demonstrated. The results indicate integrin α5 as a potent marker to discriminate patients' tumor prognosis. Consequently the integrin subunit α5 can be considered as a target for individual therapy of advanced RCC.

摘要

晚期肾细胞癌(RCC)的治疗仍然是一项重大挑战。为了进行治疗干预,有必要更深入地了解转移的具体步骤。在这种情况下,像整合素这样的膜结合受体起着决定性作用。我们通过蛋白质印迹法分析了141例透明细胞RCC患者的整合素α5表达。RCC患者肿瘤组织中整合素α5的表达水平明显高于正常组织。整合素α5表达与肿瘤分级、肿瘤肾切除术后五年内远处转移的发生以及生存率降低相关。用纤连蛋白联合或不联合抑制性抗整合素α5抗体处理高表达整合素α5的RCC细胞系Caki-1和CCF-RC1。之后分析细胞的迁移、黏附、活力以及重要的信号分子。在用整合素α5阻断抗体处理后,两种细胞系的迁移潜能均显著降低,对纤连蛋白的黏附潜能也降低。可以证明AKT和ERK1/2信号通路的作用。结果表明整合素α5是区分患者肿瘤预后的有效标志物。因此,整合素亚基α5可被视为晚期RCC个体化治疗的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/8b050c32c6db/oncotarget-08-107530-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/a1213f792f60/oncotarget-08-107530-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/86a6783de8b3/oncotarget-08-107530-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/72b8d0544c6c/oncotarget-08-107530-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/6d1cba63c674/oncotarget-08-107530-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/73bd8b7747b5/oncotarget-08-107530-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/33f2bcf15648/oncotarget-08-107530-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/780bb3df3ea7/oncotarget-08-107530-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/8b050c32c6db/oncotarget-08-107530-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/a1213f792f60/oncotarget-08-107530-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/86a6783de8b3/oncotarget-08-107530-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/72b8d0544c6c/oncotarget-08-107530-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/6d1cba63c674/oncotarget-08-107530-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/73bd8b7747b5/oncotarget-08-107530-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/33f2bcf15648/oncotarget-08-107530-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/780bb3df3ea7/oncotarget-08-107530-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9f/5746086/8b050c32c6db/oncotarget-08-107530-g008.jpg

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