Literature DB >> 10767622

Gene transfer to suppress bone marrow alkylation sensitivity.

R B Roth1, L D Samson.   

Abstract

Alkylating agents represent a highly cytotoxic class of chemotherapeutic compounds that are extremely effective anti-tumor agents. Unfortunately, alkylating agents damage both malignant and non-malignant tissues. Bone marrow is especially sensitive to damage by alkylating agent chemotherapy, and is a dose-limiting tissue when treating cancer patients. One strategy to overcome bone marrow sensitivity to alkylating agent exposure involves gene transfer of the DNA repair protein O(6)-methylguanine DNA methyltransferase (O(6)MeG DNA MTase) into bone marrow cells. O(6)MeG DNA MTase is of particular interest because it functions to protect against the mutagenic, clastogenic and cytotoxic effects of many chemotherapeutic alkylating agents. By increasing the O(6)MeG DNA MTase repair capacity of bone marrow cells, it is hoped that this tissue will become alkylation resistant, thereby increasing the therapeutic window for the selective destruction of malignant tissue. In this review, the field of O(6)MeG DNA MTase gene transfer into bone marrow cells will be summarized with an emphasis placed on strategies used for suppressing the deleterious side effects of chemotherapeutic alkylating agent treatment.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10767622     DOI: 10.1016/s1383-5742(00)00021-1

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  6 in total

1.  In vitro erythropoiesis from bone marrow-derived progenitors provides a physiological assay for toxic and mutagenic compounds.

Authors:  J Shuga; J Zhang; L D Samson; H F Lodish; L G Griffith
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-14       Impact factor: 11.205

2.  Polymorphism in glutathione S-transferase P1 is associated with susceptibility to chemotherapy-induced leukemia.

Authors:  J M Allan; C P Wild; S Rollinson; E V Willett; A V Moorman; G J Dovey; P L Roddam; E Roman; R A Cartwright; G J Morgan
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-11       Impact factor: 11.205

Review 3.  Targeting O⁶-methylguanine-DNA methyltransferase with specific inhibitors as a strategy in cancer therapy.

Authors:  Bernd Kaina; Geoffrey P Margison; Markus Christmann
Journal:  Cell Mol Life Sci       Date:  2010-08-18       Impact factor: 9.261

4.  O6-methylguanine-induced cell death involves exonuclease 1 as well as DNA mismatch recognition in vivo.

Authors:  Joanna Klapacz; Lisiane B Meira; David G Luchetti; Jennifer A Calvo; Roderick T Bronson; Winfried Edelmann; Leona D Samson
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-05       Impact factor: 11.205

5.  DNA mismatch repair in eukaryotes and bacteria.

Authors:  Kenji Fukui
Journal:  J Nucleic Acids       Date:  2010-07-27

6.  Alkyltransferase-like protein (eATL) prevents mismatch repair-mediated toxicity induced by O6-alkylguanine adducts in Escherichia coli.

Authors:  Gerard Mazon; Gaëlle Philippin; Jean Cadet; Didier Gasparutto; Mauro Modesti; Robert P Fuchs
Journal:  Proc Natl Acad Sci U S A       Date:  2010-10-04       Impact factor: 11.205

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.