The Chloroethylnitrosoureas: Sensitivity and Resistance to Cancer Chemotherapy at the Molecular Level
- 1 January 1997
- journal article
- research article
- Published by Taylor & Francis in Cancer Investigation
- Vol. 15 (6) , 588-598
- https://doi.org/10.3109/07357909709047601
Abstract
The chloroethylnitrosoureas were developed in a synthetic program that began with the observation that N-methyl-N′-nitro-N-nitrosoguanidine was an effective agent against L1210 cells. The antitumor activity of the chloroethylnitrosoureas is based on their reactions with DNA, especially the formation of a cytosine-guanine crosslink in DNA. Resistance occurs when the enzyme, O6-alkylguanine-DNA alkyltransferase, repairs an intermediate in crosslink formation. Inhibition of O6-alkylguanine-DNA alkyltransferase often restores sensitivity to the chloroethlylnitrosoureas although evidence is accumulating that other repair mechanisms may also contribute to the resistance phenomenon. Continuing investigations in this field center on finding agents whose reactions with DNA are more specific, on elucidating other resistance mechanisms, and on overcoming resistance by developing new inhibitors of repair enzymes.Keywords
This publication has 38 references indexed in Scilit:
- DNA alkylation by the haloethylnitrosoureas: Nature of modifications produced and their enzymatic repair or removalMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1990
- DNA Modification by the Nitrosoureas: Chemical Nature and Cellular RepairPublished by Springer Nature ,1985
- CHLOROZOTOCIN: CLINICAL TRIALSPublished by Elsevier ,1981
- THE DEVELOPMENT OF THE NITROSOUREAS: A STUDY IN CONGENER SYNTHESISPublished by Elsevier ,1981
- Reaction of 1,3-bis(2-chloroethyl)-1-nitrosourea with synthetic polynucleotidesBiochemistry, 1975
- Mechanism of Action of NitrosoureasPublished by Springer Nature ,1975
- Synthesis of chlorozotocin, the 2-chloroethyl analog of the anticancer antibiotic streptozotocinJournal of Medicinal Chemistry, 1975
- Reaction of BCNU (1,3-Bis (2-chloroethyl)-1-nitrosourea) with polycytidylic acid. Substitution of the cytosine ringBiochemical and Biophysical Research Communications, 1974
- 1,3-Bis(2-Chloroethyl)-1-Nitrosourea (Bcnu) And Other Nitrosoureas In Cancer Treatment: A ReviewAdvances in Cancer Research, 1973
- NITROGEN MUSTARD THERAPYJAMA, 1946