Proteomic Analysis of Nuclei Isolated from Cancer Cell Lines Treated with Indenoisoquinoline NSC 724998, a Novel Topoisomerase I Inhibitor

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• 作者：Bingnan Han ; Luke H. Stockwin ; Chad Hancock ; Sherry X. Yu ; Melinda G. Hollingshead ; Dianne L. Newton
• 刊名：Journal of Proteome Research
• 出版年：2010
• 出版时间：August 6, 2010
• 年：2010
• 卷：9
• 期：8
• 页码：4016-4027
• 全文大小：574K
• 年卷期：v.9,no.8(August 6, 2010)
• ISSN：1535-3907

文摘

The indenoisoquinoline NSC724998 is a novel topoisomerase I (Top1) inhibitor entering Phase I clinical trials at the National Cancer Institute, USA. In this study, 2-D PAGE analysis was performed on nuclear lysates prepared from HCT-116 and A375 cells treated with 1 μM NSC724998 for 24 h and the differentially regulated spots identified by LC−MS/MS. One-hundred fourteen protein spot differentials were identified, 66 from A375 cells and 48 from HCT-116 cells. Proteins related to apoptosis changed specifically in A375 cells, whereas proteins involved in the ubiquitin-proteasome system were highly enriched in treated HCT-116 cells. Importantly, 12 differentially expressed proteins (ETFA, HCC1, HNRCL, KAP1, NPM, NUCL, PRDX1, PRP19, PSB6, RAE1L, RU2A, and SFRS9) were common to both cell lines. Western blotting and immunocytochemistry confirmed significant nuclear upregulation of both the proteasome subunit PSB6 and the transcriptional repressor KAP1. Interestingly, increased KAP1 polypeptide was accompanied by enhanced phosphorylation at Ser824. Similar to γH2AX, KAP1 phosphorylation was consistently enhanced in a panel of 12 cell lines and in A375 xenografts following NSC 724998 treatment. In summary, these data enhance our understanding of protein dynamics in the nucleus following DNA damage and provide an alternate marker (pKAP1) with potential for monitoring clinical responses to Top1 poisons.

Keywords:

topoisomerase I; indenoisoquinoline; DNA damage; KAP1; proteasome; γH2AX; nuclear proteome