Suppr超能文献

工程化抗体样分子ATF-Fc与曲妥珠单抗对人乳腺癌异种移植小鼠模型肿瘤生长和侵袭的协同抑制作用

Synergistic inhibitory effects of an engineered antibody-like molecule ATF-Fc and trastuzumab on tumor growth and invasion in a human breast cancer xenograft mouse model.

作者信息

Zhou Hongwei, Wang Hongwei, Yu Guangyuan, Wang Zhihong, Zheng Xi, Duan Haifeng, Sun Junzhong

机构信息

Department of Geriatric Oncology, The First Affiliated Hospital of Chinese PLA General Hospital, Beijing 100048, P.R. China.

Department of Pathology, The First Affiliated Hospital of Chinese PLA General Hospital, Beijing 100048, P.R. China.

出版信息

Oncol Lett. 2017 Nov;14(5):5189-5196. doi: 10.3892/ol.2017.6896. Epub 2017 Sep 6.

Abstract

The overexpression of the oncogene human epidermal growth factor receptor 2 (HER-2) has been associated with decreased disease-free survival and is a marker of poor prognosis of invasive breast cancer. Although the high efficacy of trastuzumab, a drug that targets the HER-2 oncogene, has been widely recognized, the efficiency of the treatment remains at ~30%. Therefore, novel effective treatments are required for patients with recurrent metastatic breast cancer. The present study aimed to investigate the effects of an engineered antibody-like molecule administered alone or in combination with trastuzumab on the tumor growth and metastasis of HER-2-positive breast cancer. Another aim was to investigate novel cancer therapies for HER-2-positive breast cancer. The engineered antibody-like molecule consists of the amino-terminal fragment (ATF) of human urokinase-type plasminogen (uPA) and is conjugated with the Fc fragment of human immunoglobulin G1 (ATF-Fc). The anti-cancer effect of ATF-Fc (alone and in combination with trastuzumab) on tumor cells and in a nude mouse tumor model was evaluated by detecting the expression of uPA, urokinase plasminogen activator receptor (uPAR) and HER-2. experiments demonstrated that specifically blocking the uPA-uPAR and HER-2 signaling pathways may effectively promote the apoptosis of breast cancer cells. Additionally, ATF-Fc-induced cell death in HER-2-positive breast cancer cells was observed . When ATF-Fc was administered in combination with trastuzumab, cell death was increased and breast cancer metastasis was reduced. The novel engineered antibody-like molecule ATF-Fc was able to inhibit HER-2-positive breast cancer cell growth and metastasis by interfering with uPA and its receptor (uPA-uPAR) system. Additionally, the antibody-like molecule exhibits a synergistic inhibitory effect when administered in combination with trastuzumab.

摘要

致癌基因人类表皮生长因子受体2(HER-2)的过表达与无病生存期缩短相关,是浸润性乳腺癌预后不良的一个标志物。尽管靶向HER-2致癌基因的药物曲妥珠单抗具有高效性,已得到广泛认可,但治疗有效率仍维持在30%左右。因此,复发转移性乳腺癌患者需要新的有效治疗方法。本研究旨在调查一种工程化抗体样分子单独使用或与曲妥珠单抗联合使用时,对HER-2阳性乳腺癌肿瘤生长和转移的影响。另一个目的是研究HER-2阳性乳腺癌的新型癌症治疗方法。该工程化抗体样分子由人尿激酶型纤溶酶原(uPA)的氨基末端片段(ATF)组成,并与人免疫球蛋白G1的Fc片段(ATF-Fc)偶联。通过检测uPA、尿激酶纤溶酶原激活物受体(uPAR)和HER-2的表达,评估ATF-Fc(单独使用及与曲妥珠单抗联合使用)对肿瘤细胞和裸鼠肿瘤模型的抗癌作用。实验表明,特异性阻断uPA-uPAR和HER-2信号通路可有效促进乳腺癌细胞凋亡。此外,观察到ATF-Fc可诱导HER-2阳性乳腺癌细胞死亡。当ATF-Fc与曲妥珠单抗联合使用时,细胞死亡增加,乳腺癌转移减少。新型工程化抗体样分子ATF-Fc能够通过干扰uPA及其受体(uPA-uPAR)系统来抑制HER-2阳性乳腺癌细胞的生长和转移。此外,该抗体样分子与曲妥珠单抗联合使用时表现出协同抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c09/5656026/5fe0268b67d2/ol-14-05-5189-g00.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验