Literature DB >> 18322942

Feasibility of herpes simplex virus type 1 mutants labeled with radionuclides for tumor treatment.

Yan-Xia Mi1, Ya-Hong Long, Yun-Chun Li.   

Abstract

For over one hundred years, viruses have been recognized as capable of killing tumor cells. At present, people are still researching and constructing more suitable oncolytic viruses for treating different malignant tumors. Although extensive studies have demonstrated that herpes simplex virus type 1 (HSV-1) is the most potential oncolytic virus, therapies based on herpes simplex virus type 1 vectors still arouse bio-safety and risk management issues. Researchers have therefore introduced the new idea of treating cancer with HSV-1 mutants labeled with radionuclides, combining radionuclide and oncolytic virus therapies. This overview briefly summarizes the status and mechanisms by which oncolytic viruses kill tumor cells, discusses the application of HSV-1 and HSV-1 derived vectors for tumor therapy, and demonstrates the feasibility and prospect of HSV-1 mutants labeled with radionuclides for treating tumors.

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Year:  2008        PMID: 18322942      PMCID: PMC2693676          DOI: 10.3748/wjg.14.1321

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  36 in total

Review 1.  Herpes simplex virus: receptors and ligands for cell entry.

Authors:  Patricia G Spear
Journal:  Cell Microbiol       Date:  2004-05       Impact factor: 3.715

2.  Glycoprotein C-independent binding of herpes simplex virus to cells requires cell surface heparan sulphate and glycoprotein B.

Authors:  B C Herold; R J Visalli; N Susmarski; C R Brandt; P G Spear
Journal:  J Gen Virol       Date:  1994-06       Impact factor: 3.891

Review 3.  Herpes simplex virus 1 (HSV-1) for cancer treatment.

Authors:  Y Shen; J Nemunaitis
Journal:  Cancer Gene Ther       Date:  2006-04-07       Impact factor: 5.987

4.  Gene transfer of wild-type p53 results in restoration of tumor-suppressor function in a medulloblastoma cell line.

Authors:  M R Rosenfeld; P Meneses; J Dalmau; M Drobnjak; C Cordon-Cardo; M G Kaplitt
Journal:  Neurology       Date:  1995-08       Impact factor: 9.910

5.  Mutant herpes simplex virus induced regression of tumors growing in immunocompetent rats.

Authors:  M G Kaplitt; J G Tjuvajev; D A Leib; J Berk; K D Pettigrew; J B Posner; D W Pfaff; S D Rabkin; R G Blasberg
Journal:  J Neurooncol       Date:  1994       Impact factor: 4.130

6.  HSV1716 injection into the brain adjacent to tumour following surgical resection of high-grade glioma: safety data and long-term survival.

Authors:  S Harrow; V Papanastassiou; J Harland; R Mabbs; R Petty; M Fraser; D Hadley; J Patterson; S M Brown; R Rampling
Journal:  Gene Ther       Date:  2004-11       Impact factor: 5.250

7.  An adenovirus mutant that replicates selectively in p53-deficient human tumor cells.

Authors:  J R Bischoff; D H Kirn; A Williams; C Heise; S Horn; M Muna; L Ng; J A Nye; A Sampson-Johannes; A Fattaey; F McCormick
Journal:  Science       Date:  1996-10-18       Impact factor: 47.728

8.  A mutant herpes simplex virus type 1 unable to express glycoprotein L cannot enter cells, and its particles lack glycoprotein H.

Authors:  C Roop; L Hutchinson; D C Johnson
Journal:  J Virol       Date:  1993-04       Impact factor: 5.103

Review 9.  The complete DNA sequence of the long unique region in the genome of herpes simplex virus type 1.

Authors:  D J McGeoch; M A Dalrymple; A J Davison; A Dolan; M C Frame; D McNab; L J Perry; J E Scott; P Taylor
Journal:  J Gen Virol       Date:  1988-07       Impact factor: 3.891

10.  Early events in herpes simplex virus type 1 infection: photosensitivity of fluorescein isothiocyanate-treated virions.

Authors:  N DeLuca; D Bzik; S Person; W Snipes
Journal:  Proc Natl Acad Sci U S A       Date:  1981-02       Impact factor: 11.205

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