Literature DB >> 15500404

Gene therapy strategies to improve the effectiveness of cancer radiotherapy.

Svend O Freytag1, Jae Ho Kim, Stephen L Brown, Kenneth Barton, Mei Lu, Myung Chung.   

Abstract

Having the ability to alter the genetic makeup of a cancer cell by gene transfer is a potentially powerful strategy for treating human cancer. However, a low efficiency of gene delivery in vivo and poor tumour specificity has prevented the widespread implementation of this technology in the clinic. Despite these formidable obstacles, the first successful application of gene therapy in the treatment of cancer may occur when it is combined with local modalities such as radiation therapy. A small number of gene therapy strategies have been evaluated in clinical trials in combination with external beam radiation therapy. The combined therapy has been well-tolerated and has not exacerbated the side effects of radiation therapy. Gene transfer and tumour cell destruction has been demonstrated in vivo. Although the results await confirmation in larger, prospective Phase III trials, there is suggestive evidence that the combined therapies may be demonstrating better than expected antitumour activity. Our vast knowledge of the molecular defects that drive the cancer process, coupled with our expanding understanding of the genes responsible for tumour cell radioresistance, have spawned the development of rational, targeted gene therapies designed to increase tumour cell radiosensitivity. Here, the results of the clinical trials conducted so far will be reviewed, followed by a description of new approaches under development at present.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15500404     DOI: 10.1517/14712598.4.11.1757

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  5 in total

Review 1.  [The use of p53 as a tool for human cancer therapy].

Authors:  V P Almazov; D V Kochetkov; P M Chumakov
Journal:  Mol Biol (Mosk)       Date:  2007 Nov-Dec

2.  Wild-type p53 enhances the cytotoxic effect of radionuclide gene therapy using sodium iodide symporter in a murine anaplastic thyroid cancer model.

Authors:  Yong Jin Lee; June-Key Chung; Joo Hyun Kang; Jae Min Jeong; Dong Soo Lee; Myung Chul Lee
Journal:  Eur J Nucl Med Mol Imaging       Date:  2009-09-01       Impact factor: 9.236

3.  Docetaxel increases antitumor efficacy of oncolytic prostate-restricted replicative adenovirus by enhancing cell killing and virus distribution.

Authors:  Xiong Li; Youhong Liu; Yong Tang; Phipps Roger; Meei-Huey Jeng; Chinghai Kao
Journal:  J Gene Med       Date:  2010-06       Impact factor: 4.152

4.  A triple suicide gene strategy that improves therapeutic effects and incorporates multimodality molecular imaging for monitoring gene functions.

Authors:  L Xing; X Sun; X Deng; K Kotedia; P B Zanzonico; E Ackerstaff; J A Koutcher; C C Ling; G C Li
Journal:  Cancer Gene Ther       Date:  2013-05-31       Impact factor: 5.987

5.  Hypoxia-targeted triple suicide gene therapy radiosensitizes human colorectal cancer cells.

Authors:  Hung Tsung Hsiao; Ligang Xing; Xuelong Deng; Xiaorong Sun; C Clifton Ling; Gloria C Li
Journal:  Oncol Rep       Date:  2014-06-06       Impact factor: 3.906

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.