A Novel Virus-Free Anticancer Gene Therapy
非病毒性抗腫瘤基因新療法
Project Content 項目內容
Prof. TANG Ming Kuen Patrick
鄧銘權教授
Department of Anatomical and Cellular Pathology 病理解剖及細胞學系
Prof. LAN Hui Yao
藍輝耀教授
Choh-Ming Li Professor of Biomedical Sciences
卓敏生物醫學講座教授
Funding 資助機構
Innovation and Technology Commission, Research Grants Council, The Chinese University of Hong Kong Faculty of Medicine, Guangdong Science and Technology, The Lui Che Woo Institute of Innovative Medicine
創新科技署、研究資助局、香港中文大學醫學院、廣東省科技廳、呂志和創新醫學研究所
Award 獎項
Gold Medal with Congratulations of the Jury, International Exhibition of Inventions Geneva 2021
2021年日內瓦發明展評審團特別嘉許金獎
Patent 專利
1 US Provisional Filed and 1 Hong Kong Application
一項美國臨時專利及一項香港專利註冊
In our invention, the gene-silencing particles are specifically delivered to tumor by ultrasound microbubble system. 我們的無病毒基因療法,通過超聲微泡系統將基因沉默質粒傳遞至腫瘤中,精準地發揮其抗癌作用。
Our new method effectively stops the growth of human lung cancer by largely enhancing the anticancer immunity (iNOS+ F4/80) in tumor. 我們的無病毒基因療法能夠增強抗癌免疫力,有效阻止人類肺癌的生長。
CE's Reception for Awardees of International Exhibition of Inventions of Geneva 2021 「2021年日內瓦國際發明展」行政長官嘉許禮
In our invention, the gene-silencing particles are specifically delivered to tumor by ultrasound microbubble system. 我們的無病毒基因療法,通過超聲微泡系統將基因沉默質粒傳遞至腫瘤中,精準地發揮其抗癌作用。
Gene therapy conventionally utilizes virus to correct diseased genes for eliminating cancer, but safety risks and off-target effects of viral method largely limit their clinical translation.
Therefore, CUHK team combined RNA interference technology and ultrasound microbubble system to form a novel virus-free gene therapy. The invention specifically delivers gene silencing particles into tumor without using any virus. It can serve as a rapid evaluating platform for therapeutic efficiency of new gene targets preclinically, as well as development to be a safe anticancer therapy clinically.
基因療法能利用病毒修改癌變基因,但潛在臨床安全風險。因此,中大研究團隊揉合了RNA干擾技術及超聲微泡系統,成功發明出一種全新非病毒方式的抗癌基因治療。它能夠精準地靶向癌龕,有效抑制病變基因表達,過程毋須病毒。本技術能於臨床前評估抗癌效率,亦可發展成安全的臨床基因治療。
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