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使用白蛋白微球对非小细胞肺癌进行 EphA2 靶向瘤内治疗。

EphA2 targeted intratumoral therapy for non-small cell lung cancer using albumin mesospheres.

作者信息

Lee Hung-Yen, Mohammed Kamal A, Kaye Fredric, Moudgil Brij M, Nasreen Najmunnisa

机构信息

Division of Pulmonary, Critical Care & Sleep Medicine, Department of Medicine, University of FloridaGainesville, FL, USA.

Biomaterials Center, Department of Materials Sciences and Engineering, University of FloridaGainesville, FL, USA.

出版信息

Am J Transl Res. 2017 Jul 15;9(7):3293-3303. eCollection 2017.

Abstract

Lung cancer, primarily non-small cell lung cancer (NSCLC), is the leading cause of cancer mortality and the prognosis of patients with advanced or metastatic NSCLC is poor. Despite significant advances in diagnosis and treatment, little improvement has been seen in NSCLC mortality. Recently, Intratumoral Chemotherapy, a direct local delivery of chemotherapeutic drugs, has shown promise in clinical studies. However, toxicity and high dosage of chemotherapeutic agents used for treatment are a limitation. Moreover, these drugs damage indiscriminately, cancerous as well as normal tissues. Thus, a novel therapeutic strategy that targets only malignant tissue sparing normal tissue becomes an urgent issue. Ephrin receptor-A2 (EphA2), a new biomarker, is over-expressed in NSCLC, but not on normal epithelial cells. Receptor EphA2 is a cell surface protein, which upon binding to its ligand EphrinA1 undergo phosphorylation and degradation which attenuates NSCLC growth. Targeting the tumor, sparing the normal tissue and enhancing the therapeutic effects of ligand proteins are the goal of this project. Thus a novel method, intratumoral EphA2 targeted therapy, has been developed to target the oncogenic receptors on tumor tissue by using albumin mesosphere (AMS) conjugated ephrinA1 in mice bearing NSCLC tumors.

摘要

肺癌,主要是非小细胞肺癌(NSCLC),是癌症死亡的主要原因,晚期或转移性NSCLC患者的预后较差。尽管在诊断和治疗方面取得了重大进展,但NSCLC死亡率几乎没有改善。最近,瘤内化疗,即直接局部递送化疗药物,在临床研究中显示出前景。然而,用于治疗的化疗药物的毒性和高剂量是一个限制因素。此外,这些药物会不加区分地损害癌组织和正常组织。因此,一种仅针对恶性组织而 sparing正常组织的新型治疗策略成为一个紧迫的问题。Ephrin受体-A2(EphA2)是一种新的生物标志物,在NSCLC中过度表达,但在正常上皮细胞上不表达。受体EphA2是一种细胞表面蛋白,当其与配体EphrinA1结合时会发生磷酸化和降解,从而减弱NSCLC的生长。靶向肿瘤、 sparing正常组织并增强配体蛋白的治疗效果是本项目的目标。因此,已经开发出一种新方法,即瘤内EphA2靶向治疗,通过在携带NSCLC肿瘤的小鼠中使用白蛋白中层(AMS)偶联的EphrinA1来靶向肿瘤组织上的致癌受体。 (注:原文中“sparing”应为“sparing”,翻译时已修正)

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