학술논문
Autocyclized and oxidized forms of SCR7 induce cancer cell death by inhibiting nonhomologous DNA end joining in a Ligase IV dependent manner.
Document Type
Article
Author
Vartak, Supriya V.; Swarup, Hassan A.; Gopalakrishnan, Vidya; Gopinatha, Vindya K.; Ropars, Virginie; Nambiar, Mridula; John, Franklin; Kothanahally, Sharath Kumar S.; Kumari, Rupa; Kumari, Nitu; Ray, Ujjayinee; Radha, Gudapureddy; Dinesh, Depina; Pandey, Monica; Ananda, Hanumappa; Karki, Subhas S.; Srivastava, Mrinal; Charbonnier, Jean Baptiste; Choudhary, Bibha; Mantelingu, Kempegowda
Source
Subject
*CELL death
*CANCER cells
*MOLECULAR structure
*SINGLE-strand DNA breaks
*TUMOR growth
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Language
ISSN
1742-464X
Abstract
Nonhomologous DNA end joining (NHEJ) is the major DNA double‐strand break (DSB) repair pathway in mammals. Previously, we have described a small molecule inhibitor, SCR7, which can inhibit NHEJ in a Ligase IV‐dependent manner. Administration of SCR7 within the cells resulted in the accumulation of DNA breaks, cell death, and inhibition of tumor growth in mice. In the present study, we report that parental SCR7, which is unstable, can be autocyclized into a stable form. Both parental SCR7 and cyclized SCR7 possess the same molecular weight (334.09) and molecular formula (C18H14N4OS), whereas its oxidized form, SCR7‐pyrazine, possesses a different molecular formula (C18H12N4OS), molecular weight (332.07), and structure. While cyclized form of SCR7 showed robust inhibition of NHEJ in vitro, both forms exhibited efficient cytotoxicity. Cyclized and oxidized forms of SCR7 inhibited DNA end joining catalyzed by Ligase IV, whereas their impact was minimal on Ligase III, Ligase I, and T4 DNA Ligase‐mediated joining. Importantly, both forms inhibited V(D)J recombination, although the effect was more pronounced for SCR7‐cyclized. Both forms blocked NHEJ in a Ligase IV‐dependent manner leading to the accumulation of DSBs within the cells. Although cytotoxicity due to SCR7‐cyclized was Ligase IV specific, the pyrazine form exhibited nonspecific cytotoxicity at higher concentrations in Ligase IV‐null cells. Finally, we demonstrate that both forms can potentiate the effect of radiation. Thus, we report that cyclized and oxidized forms of SCR7 can inhibit NHEJ in a Ligase IV‐dependent manner, although SCR7‐pyrazine is less specific to Ligase IV inside the cell. Nonhomologous DNA end joining (NHEJ) is the major DNA DSB repair pathway in mammals. We show that parental SCR7 gets autocyclized to stable SCR7‐cyclized, with the same molecular weight, molecular mass, and melting point, which upon oxidation, forms SCR7‐pyrazine having a different molecular weight, molecular mass, and melting point. Although both forms inhibit NHEJ in a Ligase IV‐dependent manner in vitro and induce cytotoxicity, SCR7‐pyrazine can be nonspecific inside the cell. [ABSTRACT FROM AUTHOR]