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Silencing of Receptor Tyrosine Kinase ROR1 Inhibits Tumor-Cell Proliferation via PI3K/AKT/mTOR Signaling Pathway in Lung Adenocarcinoma

机译:受体酪氨酸激酶ROR1的沉默抑制肺腺癌中通过PI3K / AKT / mTOR信号通路的肿瘤细胞增殖。

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摘要

Receptor tyrosine kinase ROR1, an embryonic protein involved in organogenesis, is expressed in certain hematological malignancies and solid tumors, but is generally absent in adult tissues. This makes the protein an ideal drug target for cancer therapy. In order to assess the suitability of ROR1 as a cell surface antigen for targeted therapy of lung adenocarcinoma, we carried out a comprehensive analysis of ROR1 protein expression in human lung adenocarcinoma tissues and cell lines. Our data show that ROR1 protein is selectively expressed on lung adenocarcinoma cells, but do not support the hypothesis that expression levels of ROR1 are associated with aggressive disease. However silencing of ROR1 via siRNA treatment significantly down-regulates the activity of the PI3K/AKT/mTOR signaling pathway. This is associated with significant apoptosis and anti-proliferation of tumor cells. We found ROR1 protein expressed in lung adenocarcinoma but almost absent in tumor-adjacent tissues of the patients. The finding of ROR1-mediated proliferation signals in both tyrosine kinase inhibitor (TKI)-sensitive and -resistant tumor cells provides encouragement to develop ROR1-directed targeted therapy in lung adenocarcinoma, especially those with TKI resistance.
机译:受体酪氨酸激酶ROR1(一种参与器官发生的胚胎蛋白)在某些血液系统恶性肿瘤和实体瘤中表达,但在成人组织中通常不存在。这使蛋白质成为癌症治疗的理想药物靶标。为了评估ROR1作为细胞表面抗原用于肺腺癌靶向治疗的适用性,我们对人肺腺癌组织和细胞系中ROR1蛋白表达进行了全面分析。我们的数据表明ROR1蛋白在肺腺癌细胞上选择性表达,但不支持ROR1表达水平与侵袭性疾病相关的假设。但是,通过siRNA处理使ROR1沉默会显着下调PI3K / AKT / mTOR信号通路的活性。这与肿瘤细胞的显着凋亡和抗增殖有关。我们发现ROR1蛋白在肺腺癌中表达,但在患者的肿瘤邻近组织中几乎不存在。在酪氨酸激酶抑制剂(TKI)敏感和耐药的肿瘤细胞中ROR1介导的增殖信号的发现为在肺腺癌,特别是那些具有TKI耐药性的肺癌中发展ROR1导向的靶向治疗提供了鼓励。

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