Literature DB >> 8607033

p53 gene therapy in vivo of herpatocellular and liver metastatic colorectal cancer.

R Bookstein1, W Demers, R Gregory, D Maneval, J Park, K Wills.   

Abstract

Tumor suppressor genes such as p53 contribute to the oncogenic process via loss-of-function mechanisms such as genetic mutation or complex formation with other cellular or viral proteins. p53 is mutated in approximately 50% of human tumors and has an important role in the genesis or progression of both colorectal and hepatocellular cancers. Colorectal cancer is leading cause of cancer mortality in the United States, whereas hepatocellular cancer is the leading worldwide cause of cancer death; the liver is a primary site of morbidity in both diseases. Because systemic tumor suppressor gene therapy is currently not feasible, we have chosen to develop a regional form of such therapy directed at primary or metastatic liver neoplasms. Gene replacement therapy with p53 is a promising new strategy to treat advanced human cancers.

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Year:  1996        PMID: 8607033

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  7 in total

Review 1.  Gene therapy: regulations, ethics and its practicalities in liver disease.

Authors:  Xi Jin; Yi-Da Yang; You-Ming Li
Journal:  World J Gastroenterol       Date:  2008-04-21       Impact factor: 5.742

Review 2.  Localized hepatocellular carcinoma: therapeutic options.

Authors:  A Ribeiro; D M Nagorney; G J Gores
Journal:  Curr Gastroenterol Rep       Date:  2000-02

3.  Adenovirus mediated p53 tumour suppressor gene therapy for human gastric cancer cells in vitro and in vivo.

Authors:  M Ohashi; F Kanai; H Ueno; T Tanaka; K Tateishi; T Kawakami; Y Koike; T Ikenoue; Y Shiratori; H Hamada; M Omata
Journal:  Gut       Date:  1999-03       Impact factor: 23.059

4.  Interferon-beta gene therapy inhibits tumor formation and causes regression of established tumors in immune-deficient mice.

Authors:  X Q Qin; N Tao; A Dergay; P Moy; S Fawell; A Davis; J M Wilson; J Barsoum
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-24       Impact factor: 11.205

5.  Synergistic anticancer effect of exogenous wild-type p53 gene combined with 5-FU in human colon cancer resistant to 5-FU in vivo.

Authors:  Qi Xie; Min-Yi Wu; Ding-Xuan Zhang; Yi-Ming Yang; Bao-Shuai Wang; Jing Zhang; Jin Xu; Wei-De Zhong; Jia-Ni Hu
Journal:  World J Gastroenterol       Date:  2016-08-28       Impact factor: 5.742

6.  In vivo recombinant adenovirus-mediated p53 gene therapy in a syngeneic rat model for colorectal cancer.

Authors:  Jeong-Heum Baek; Munna L Agarwal; Raymond R Tubbs; Alex Vladisavljevic; Hiroshi Tomita; Ronald M Bukowski; Jeffrey W Milsom; Jin-Man Kim; Jin-Young Kwak
Journal:  J Korean Med Sci       Date:  2004-12       Impact factor: 2.153

7.  Killing of p53-deficient hepatoma cells by parvovirus H-1 and chemotherapeutics requires promyelocytic leukemia protein.

Authors:  Maike Sieben; Kerstin Herzer; Maja Zeidler; Vera Heinrichs; Barbara Leuchs; Martin Schuler; Jan-J Cornelis; Peter-R Galle; Jean Rommelaere; Markus Moehler
Journal:  World J Gastroenterol       Date:  2008-06-28       Impact factor: 5.742

  7 in total

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