Literature DB >> 14601515

The role of gene therapy in combined modality treatment strategies for cancer.

Bingliang Fang1, Jack A Roth.   

Abstract

Multimodality therapy has been widely used in cancer treatment for enhancing efficacy, reducing toxicity, and preventing or delaying development of resistance. However, as the difference in biochemical signals between normal and malignant cells is usually trivial, combinations of conventional therapies often cause intolerably high levels of toxicity in most cancer patients. Gene therapy uses genetically encoded functions to attack molecular events involved in the development and maintenance of malignancies, providing a molecular approach to eradicate cancer cells or to protect normal cells from the toxicity of conventional therapies. Furthermore, gene therapy can also be used to augment biochemical signals required for effective chemotherapy and radiotherapy. Recent preclinical studies have shown that synergistic effects can be achieved by combining gene therapy and conventional anticancer therapies. Moreover, several phase I/II clinical studies have demonstrated that anticancer gene therapy is well tolerated and that combining gene therapy with chemotherapy, radiotherapy, or both, resulted in enhanced antitumor activity without increased toxicity. Favorable clinical responses, including a pathologically complete response, have been reported in a subset of patients with advanced disease or with cancers resistant to chemotherapy or radiotherapy. Thus, combining gene therapy and conventional therapies may provide an improvement in the treatment of cancers, especially for those resistant to conventional therapies. This review focuses on the most recent achievements in cancer treatment by combining gene therapy with conventional therapies.

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Mesh:

Year:  2003        PMID: 14601515

Source DB:  PubMed          Journal:  Curr Opin Mol Ther        ISSN: 1464-8431


  6 in total

1.  Dual cancer-specific targeting strategy cures primary and distant breast carcinomas in nude mice.

Authors:  Devanand Sarkar; Zao-Zhong Su; Nicolaq Vozhilla; Eun Sook Park; Pankaj Gupta; Paul B Fisher
Journal:  Proc Natl Acad Sci U S A       Date:  2005-09-19       Impact factor: 11.205

2.  RYBP predicts survival of patients with non-small cell lung cancer and regulates tumor cell growth and the response to chemotherapy.

Authors:  Sukesh Voruganti; Fangxiu Xu; Jiang-Jiang Qin; Yan Guo; Sushanta Sarkar; Ming Gao; Zhijie Zheng; Ming-Hai Wang; Jianwei Zhou; Biyun Qian; Ruiwen Zhang; Wei Wang
Journal:  Cancer Lett       Date:  2015-09-21       Impact factor: 8.679

3.  Radiotherapy sensitization by tumor-specific TRAIL gene targeting improves survival of mice bearing human non-small cell lung cancer.

Authors:  Xiaochun Zhang; Rex Min Cheung; Ritsuko Komaki; Bingliang Fang; Joe Y Chang
Journal:  Clin Cancer Res       Date:  2005-09-15       Impact factor: 12.531

4.  RNA interference-mediated silencing of the polo-like kinase 1 gene enhances chemosensitivity to gemcitabine in pancreatic adenocarcinoma cells.

Authors:  C Yu; X Zhang; G Sun; X Guo; H Li; Y You; J L Jacobs; K Gardner; D Yuan; Z Xu; Q Du; C Dai; Z Qian; K Jiang; Y Zhu; Q Q Li; Y Miao
Journal:  J Cell Mol Med       Date:  2008-02-05       Impact factor: 5.310

5.  RYBP expression is associated with better survival of patients with hepatocellular carcinoma (HCC) and responsiveness to chemotherapy of HCC cells in vitro and in vivo.

Authors:  Wei Wang; Jianwen Cheng; Jiang-Jiang Qin; Sukesh Voruganti; Subhasree Nag; Jia Fan; Qiang Gao; Ruiwen Zhang
Journal:  Oncotarget       Date:  2014-11-30

6.  Overexpression of Wnt7a enhances radiosensitivity of non-small-cell lung cancer via the Wnt/JNK pathway.

Authors:  Pingping Ai; Xianhua Xu; Shijie Xu; Zhixia Wei; Shun Tan; Junzhe Li
Journal:  Biol Open       Date:  2020-06-27       Impact factor: 2.422

  6 in total

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