Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Elise Champeil"'
Publikováno v:
Journal of Nucleic Acids, Vol 2010 (2010)
The clinically used antitumor agent mitomycin C (MC) alkylates DNA upon reductive activation, forming six covalent DNA adducts in this process. This review focuses on differential biological effects of individual adducts in various mammalian cell cul
Externí odkaz:
https://doaj.org/article/9af043799f2e46e69a54d4fb89e9d34e
Autor:
Manuel M. Paz, Elise Champeil
Publikováno v:
Chemical record (New York, N.Y.).
Mitomycin C, (MC), an antitumor drug used in the clinics, is a DNA alkylating agent. Inert in its native form, MC is reduced to reactive mitosenes in cellulo which undergo nucleophilic attack by DNA bases to form monoadducts as well as interstrand cr
Publikováno v:
The FASEB Journal. 36
Publikováno v:
The FASEB Journal. 36
Autor:
Marian Romaine, Ana G. Petrovic, Manuel M. Paz, Elise Champeil, Gloria Proni, Rinat R. Abzalimov, Owen Zacarias, William Aguilar
Publikováno v:
Chemistry
Mitomycin C, (MC), an antitumor drug and decarbamoylmitomycin C, (DMC), a derivative of MC lacking the carbamoyl moiety, are DNA alkylating agents which can form DNA interstrand crosslinks (ICLs) between deoxyguanosine residues located on opposing DN
Autor:
Shu-Yuan Cheng, Lissette Delgado-Cruzata, Cristina C. Clement, Owen Zacarias, Marta Concheiro-Guisan, Nicholas Towler, Timothy Snyder, Maggie Zheng, Nickolas Almodovar, Christina Gonzalez, Marian Romaine, Anne-Marie Sapse, Elise Champeil
Publikováno v:
Bioorg Chem
While interstrand crosslinks (ICLs) have been considered as one type of DNA damage in the past, there is mounting evidence suggesting that these highly cytotoxic lesions are processed differently by the cellular machinery depending upon the ICL struc
Publikováno v:
Chemistry
Mitomycin C, (MC), an antitumor drug, is a DNA alkylating agent currently used in the clinics. Inert in its native form, MC is reduced to reactive mitosenes, which undergo nucleophilic attack by guanine or adenine bases in DNA to form monoadducts as
Autor:
Manuel M. Paz, Elise Champeil, Maggie Zheng, William Aguilar, Sergey Tsukanov, Shu-Yuan Cheng, Padmanava Pradhan, Owen Zacarias
Publikováno v:
Chemical Research in Toxicology. 31:762-771
Mitomycin C (MC) is an anticancer agent that alkylates DNA to form monoadducts and interstrand cross-links. Decarbamoylmitomycin C (DMC) is an analogue of MC lacking the carbamate on C10. The major DNA adducts isolated from treatment of culture cells
Autor:
Maggie Zheng, Seokjin Hwang, Timothy Snyder, Jake Aquilina, Gloria Proni, Manuel M. Paz, Padmanava Pradhan, Shu-Yuan Cheng, Elise Champeil
Publikováno v:
Bioorg Chem
Mitomycin C (MC), an anti-cancer drug, and its analog, decarbamoylmitomycin C (DMC), are DNA-alkylating agents. MC is currently used in the clinics and its cytotoxicity is mainly due to its ability to form Interstrand Crosslinks (ICLs) which impede D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbad4431b02bb536644de398ab3feb14
https://europepmc.org/articles/PMC6936608/
https://europepmc.org/articles/PMC6936608/
Publikováno v:
International Journal of Oncology
Mitomycin C (MC), a commonly used anticancer drug, induces DNA damage via DNA alkylation. Decarbamoyl mitomycin C (DMC), another mitomycin lacking the carbamate at C10, generates similar lesions as MC. Interstrand cross-links (ICLs) are believed to b