Pranjol Md Zahidul Islam, Hajitou Amin
Institute of Clinical and Biomedical Science, University of Exeter Medical School, Exeter, Devon EX1 2LU, UK.
Phage Therapy Group, Department of Medicine, Burlington Danes Building, Imperial College London, Hammersmith Hospital, Du Cane Road, London W12 0NN, UK.
Viruses. 2015 Jan 19;7(1):268-84. doi: 10.3390/v7010268.
Cancer gene therapy expanded and reached its pinnacle in research in the last decade. Both viral and non-viral vectors have entered clinical trials, and significant successes have been achieved. However, a systemic administration of a vector, illustrating safe, efficient, and targeted gene delivery to solid tumors has proven to be a major challenge. In this review, we summarize the current progress and challenges in the targeted gene therapy of cancer. Moreover, we highlight the recent developments of bacteriophage-derived vectors and their contributions in targeting cancer with therapeutic genes following systemic administration.
癌症基因治疗在过去十年中得到了扩展并达到了研究的顶峰。病毒载体和非病毒载体都已进入临床试验,并取得了显著成功。然而,事实证明,要实现载体的全身给药,即安全、高效且靶向地将基因递送至实体瘤,是一项重大挑战。在本综述中,我们总结了癌症靶向基因治疗的当前进展和挑战。此外,我们重点介绍了噬菌体衍生载体的最新进展及其在全身给药后用治疗性基因靶向癌症方面的贡献。