Kennedy Daniel R, Ju Jianhua, Shen Ben, Beerman Terry A
Department of Pharmacology and Therapeutics, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
Proc Natl Acad Sci U S A. 2007 Nov 6;104(45):17632-7. doi: 10.1073/pnas.0708274104. Epub 2007 Oct 31.
The ability of the radiomimetic anticancer enediyne C-1027 to induce ataxia-telangiectasia mutated (ATM) and ATM and Rad3-related (ATR)-independent damage responses was discovered to reside in its unique ability to concurrently generate robust amounts of double-strand breaks (DSBs) and interstrand cross-links (ICLs) in cellular DNA. Furthermore, a single substitution to the chromophore's benzoxazolinate moiety shifted DNA damage to primarily ICLs and an ATR- but not ATM-dependent damage response. In contrast, single substitutions of the chromophore's beta-amino acid component shifted DNA damage to primarily DSBs, consistent with its induction of conventional ATM-dependent damage responses of the type generated by ionizing radiation and other radiomimetics. Thus, phosphatidylinositol 3-kinase-like protein kinase regulation of DNA damage responses is dictated by the relative proportions of DSBs and ICLs.
放射模拟抗癌烯二炔C-1027诱导共济失调毛细血管扩张突变(ATM)以及ATM和Rad3相关(ATR)非依赖性损伤反应的能力,被发现源于其在细胞DNA中同时产生大量双链断裂(DSB)和链间交联(ICL)的独特能力。此外,发色团苯并恶唑啉部分的单个取代将DNA损伤主要转变为ICL,并引发ATR而非ATM依赖性损伤反应。相比之下,发色团β-氨基酸组分的单个取代将DNA损伤主要转变为DSB,这与其诱导由电离辐射和其他放射模拟物产生的常规ATM依赖性损伤反应一致。因此,DNA损伤反应的磷脂酰肌醇3激酶样蛋白激酶调节由DSB和ICL的相对比例决定。