Literature DB >> 10052349

Improving enzymes for cancer gene therapy.

L P Encell1, D M Landis, L A Loeb.   

Abstract

New techniques now make it feasible to tailor enzymes for cancer gene therapy. Novel enzymes with desired properties can be created and selected from vast libraries of mutants containing random substitutions within catalytic domains. In this review, we first consider genes for the ablation of tumors, namely, genes that have been mutated (or potentially can be mutated) to afford enhanced activation of prodrugs and increased sensitization of tumors to specific chemotherapeutic agents. We then consider genes that have been mutated to provide better protection of normal host tissues, such as bone marrow, against the toxicity of specific chemotherapeutic agents. Expression of the mutant enzyme could render sensitive tissues, such as bone marrow, more resistant to specific cytotoxic agents.

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Year:  1999        PMID: 10052349     DOI: 10.1038/6142

Source DB:  PubMed          Journal:  Nat Biotechnol        ISSN: 1087-0156            Impact factor:   54.908


  12 in total

Review 1.  Prodrug-activating systems in suicide gene therapy.

Authors:  C J Springer; I Niculescu-Duvaz
Journal:  J Clin Invest       Date:  2000-05       Impact factor: 14.808

2.  DNA polymerase active site is highly mutable: evolutionary consequences.

Authors:  P H Patel; L A Loeb
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-09       Impact factor: 11.205

Review 3.  Enzymes to die for: exploiting nucleotide metabolizing enzymes for cancer gene therapy.

Authors:  Andressa Ardiani; Adam J Johnson; Hongmei Ruan; Marilyn Sanchez-Bonilla; Kinta Serve; Margaret E Black
Journal:  Curr Gene Ther       Date:  2012-04-01       Impact factor: 4.391

4.  Magnetic nanoparticle hyperthermia induced cytosine deaminase expression in microencapsulated E. coli for enzyme-prodrug therapy.

Authors:  Krishnamurthy V Nemani; Riley C Ennis; Karl E Griswold; Barjor Gimi
Journal:  J Biotechnol       Date:  2015-03-25       Impact factor: 3.307

5.  Active and alkylated human AGT structures: a novel zinc site, inhibitor and extrahelical base binding.

Authors:  D S Daniels; C D Mol; A S Arvai; S Kanugula; A E Pegg; J A Tainer
Journal:  EMBO J       Date:  2000-04-03       Impact factor: 11.598

Review 6.  Introduction to the background, principles, and state of the art in suicide gene therapy.

Authors:  Ion Niculescu-Duvaz; Caroline J Springer
Journal:  Mol Biotechnol       Date:  2005-05       Impact factor: 2.695

7.  Applied molecular evolution of O6-benzylguanine-resistant DNA alkyltransferases in human hematopoietic cells.

Authors:  B M Davis; L P Encell; S P Zielske; F C Christians; L Liu; S E Friebert; L A Loeb; S L Gerson
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-10       Impact factor: 11.205

8.  Covalent capture of a human O(6)-alkylguanine alkyltransferase-DNA complex using N(1),O(6)-ethanoxanthosine, a mechanism-based crosslinker.

Authors:  D M Noll; N D Clarke
Journal:  Nucleic Acids Res       Date:  2001-10-01       Impact factor: 16.971

9.  Molecularly evolved thymidylate synthase inhibits 5-fluorodeoxyuridine toxicity in human hematopoietic cells.

Authors:  Jason H Bielas; Michael W Schmitt; Amalia Icreverzi; Nolan G Ericson; Lawrence A Loeb
Journal:  Hum Gene Ther       Date:  2009-12       Impact factor: 5.695

10.  Substrate binding pocket residues of human alkyladenine-DNA glycosylase critical for methylating agent survival.

Authors:  Cheng-Yao Chen; Haiwei H Guo; Dharini Shah; A Blank; Leona D Samson; Lawrence A Loeb
Journal:  DNA Repair (Amst)       Date:  2008-08-29
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