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基于慢病毒载体的头颈癌治疗(综述)

Lentiviral vector-based therapy in head and neck cancer (Review).

作者信息

Upreti Deepak, Pathak Alok, Kung Sam K P

机构信息

Department of Immunology, Faculty of Medicine, University of Manitoba, Winnipeg, MB R3E 0T5, Canada.

Department of Surgery, Faculty of Medicine, University of Manitoba, Winnipeg, MB R3E 0T5, Canada.

出版信息

Oncol Lett. 2014 Jan;7(1):3-9. doi: 10.3892/ol.2013.1652. Epub 2013 Nov 1.

Abstract

Head and neck squamous cell carcinoma (HNSCC) is the sixth most common neoplasm worldwide. Despite advances in multimodality treatments involving surgery, radiation and chemotherapy, the five-year survival rate has remained at ~50% for the past 35 years. Therefore, the early detection of recurrent or persistent disease is extremely important. Replication-incompetent HIV-1-based lentiviral vectors have emerged as powerful and safe tools for gene delivery. Commonly, HNSCC is a locoregional disease that presents at or close to the body surface. Thus, HNSCC is amendable to intratumoral injections of gene therapy vectors aimed at correcting defects associated with tumor suppressor genes to induce the direct cytotoxicity of cancer cells or immune modulation to promote antitumor immunity. Current investigations analyzing HNSCC gene mutations and stem cell markers and the cancer immunoediting concept are creating exciting therapeutic opportunities for lentiviral and other gene transfer vectors. The present review reports specific examples of the current applications of lentiviral vectors in HNSCC.

摘要

头颈部鳞状细胞癌(HNSCC)是全球第六大常见肿瘤。尽管在涉及手术、放疗和化疗的多模态治疗方面取得了进展,但在过去35年中,五年生存率一直保持在50%左右。因此,早期发现复发或持续性疾病极为重要。基于无复制能力的HIV-1慢病毒载体已成为强大且安全的基因递送工具。通常,HNSCC是一种局部区域性疾病,出现在体表或靠近体表的部位。因此,HNSCC适合瘤内注射基因治疗载体,旨在纠正与肿瘤抑制基因相关的缺陷,以诱导癌细胞的直接细胞毒性或免疫调节,从而促进抗肿瘤免疫。目前对HNSCC基因突变、干细胞标志物以及癌症免疫编辑概念的研究,为慢病毒和其他基因转移载体创造了令人兴奋的治疗机会。本综述报告了慢病毒载体在HNSCC当前应用的具体实例。

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