Designed enediynes: a new class of DNA-cleaving molecules with potent and selective anticancer activity
- PMID: 1589797
- DOI: 10.1126/science.256.5060.1172
Designed enediynes: a new class of DNA-cleaving molecules with potent and selective anticancer activity
Abstract
The rational design and biological actions of a new class of DNA-cleaving molecules with potent and selective anticancer activity are reported. These relatively simple enediyne-type compounds were designed from basic chemical principles to mimic the actions of the rather complex naturally occurring enediyne anticancer antibiotics, particularly dynemicin A. Equipped with locking and triggering devices, these compounds damage DNA in vitro and in vivo on activation by chemical or biological means. Their damaging effects are manifested in potent anticancer activity with remarkable selectivities. Their mechanism of action involves intracellular unlocking and triggering of a Bergman reaction, leading to highly reactive benzenoid diradicals that cause severe DNA damage. The results of these studies demonstrate the potential of these de novo designed molecules as biotechnology tools and anticancer agents.
Similar articles
-
Chemistry and biology of natural and designed enediynes.Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):5881-8. doi: 10.1073/pnas.90.13.5881. Proc Natl Acad Sci U S A. 1993. PMID: 8327459 Free PMC article. Review.
-
Structure-activity relationships of cyclic enediynes related to dynemicin A. II. Synthesis and antitumor activity of 9- and 12-substituted enediynes equipped with aryl carbamate moieties.Bioorg Med Chem. 1997 May;5(5):903-19. doi: 10.1016/s0968-0896(97)00027-8. Bioorg Med Chem. 1997. PMID: 9208101
-
Synthesis and biological evaluation of novel cyclic enediyne compounds related to dynemicin A as antitumor agents.Chem Pharm Bull (Tokyo). 1997 Jan;45(1):125-33. doi: 10.1248/cpb.45.125. Chem Pharm Bull (Tokyo). 1997. PMID: 9023974
-
Enediyne compounds - new promises in anticancer therapy.Acta Pharm. 2007 Jun;57(2):133-50. doi: 10.2478/v10007-007-0011-y. Acta Pharm. 2007. PMID: 17507311 Review.
-
Cell-specific regulation of apoptosis by designed enediynes.Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3142-6. doi: 10.1073/pnas.90.8.3142. Proc Natl Acad Sci U S A. 1993. PMID: 8475052 Free PMC article.
Cited by
-
Mechanisms of target selection by DNA-damaging chemicals: studies with enediyne anticancer drugs.Int Arch Occup Environ Health. 1996;68(6):408-14. doi: 10.1007/BF00377861. Int Arch Occup Environ Health. 1996. PMID: 8891777 Review. No abstract available.
-
Tunable and Photoactivatable Mimics of Calicheamicin γ1 for DNA Cleavage.J Am Chem Soc. 2024 Sep 18;146(37):25416-25421. doi: 10.1021/jacs.4c07754. Epub 2024 Sep 9. J Am Chem Soc. 2024. PMID: 39248674 Free PMC article.
-
Highly selective cross-coupling reactions of 1,1-dibromoethylenes with alkynylaluminums for the synthesis of aryl substituted conjugated enediynes and unsymmetrical 1,3-diynes.RSC Adv. 2022 May 3;12(21):13314-13318. doi: 10.1039/d2ra02127g. eCollection 2022 Apr 28. RSC Adv. 2022. PMID: 35520111 Free PMC article.
-
Specific inhibition of formation of transcription complexes by a calicheamicin oligosaccharide: a paradigm for the development of transcriptional antagonists.Proc Natl Acad Sci U S A. 1994 Sep 27;91(20):9203-7. doi: 10.1073/pnas.91.20.9203. Proc Natl Acad Sci U S A. 1994. PMID: 7937742 Free PMC article.
-
Biosynthesis of alkyne-containing natural products.RSC Chem Biol. 2020 Dec 21;2(1):166-180. doi: 10.1039/d0cb00190b. eCollection 2021 Feb 1. RSC Chem Biol. 2020. PMID: 34458779 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials