کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10900044 | 1084458 | 2012 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
A novel obatoclax derivative, SC-2001, induces apoptosis in hepatocellular carcinoma cells through SHP-1-dependent STAT3 inactivation
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کلمات کلیدی
STAT3DMEMFBSESIHRMSPARPSHP-1SOCSnuclear magnetic resonance - رزونانس مغناطیسی هستهایHCC - HCCLC/MS - LC / MSObatoclax - اوتاتاکلاکسNMR - تشدید مغناطیسی هستهای fetal bovine serum - سرم جنین گاوsuppressor of cytokine signaling - سرکوب کننده سیگنالینگ سیتوکینhigh-resolution mass spectrometry - طیف سنجی جرمی با وضوح بالاSignal transducers and activators of transcription 3 - مبدل های سیگنال و فعال کننده های رونویسی 3Dulbecco’s modified eagle’s medium - محیط عقاب اصلاح شده Dulbeccopoly ADP-ribose polymerase - پلی ADA-ribose پلیمرازHepatocellular carcinoma - کارسینوم هپاتوسلولار(کارسینوم سلولهای استخوانی)Liquid chromatography/mass spectrometry - کروماتوگرافی مایع / طیف سنج جرمی
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
تحقیقات سرطان
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
We investigated the effects of a novel compound, SC-2001, on hepatocellular carcinoma (HCC). SC-2001, which is structurally related to the Mcl-1 inhibitor obatoclax, showed better antitumor effects than obatoclax in HCC cell lines, including HepG2, PLC5 and Huh-7. Like obatoclax, SC-2001 inhibited the protein-protein interactions between Mcl-1 and Bak. However, SC-2001 downregulated the protein levels of Mcl-1 by reducing its transcription whereas obatoclax had no significant effect on Mcl-1 expression. As Mcl-1 is regulated by signal transducers and activators of transcription 3 (STAT3), we found that SC-2001 downregulated the phosphorylation of STAT3 (Tyr 705) and subsequently inhibited transcriptional activities of STAT3 in a dose-dependent manner. In addition to Mcl-1, STAT3-regulated proteins, including survivin and cyclin D1, were also repressed by SC-2001. Notably, SC-2001 reduced IL-6-induced STAT3 activation in HepG2 and PLC5 cells. Ectopic expression of STAT3 abolished the prominent apoptotic death in SC-2001-treated PLC5 cells, indicating that STAT3 is indispensable in mediating the effects of SC-2001. Importantly, SC-2001 enhanced the expression of SHP1, a negative regulator of STAT3. Inhibition of SHP-1 by either specific inhibitor or small interference RNA reduced the apoptotic effects of SC-2001, indicating that SHP-1 plays a key role in mediating SC2001-induced cell death. SC-2001 enhanced the activity of SHP-1 in all tested HCC cells including HepG2, PLC5 and Huh-7. Finally, SC-2001 reduced PLC5 tumor growth, downregulated p-STAT3 and upregulated SHP-1 expression and activity in vivo. In conclusion, our results suggest that SC-2001 induces apoptosis in HCC, and that this effect is mediated through SHP-1-dependent STAT3 inactivation.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Cancer Letters - Volume 321, Issue 1, 1 August 2012, Pages 27-35
Journal: Cancer Letters - Volume 321, Issue 1, 1 August 2012, Pages 27-35
نویسندگان
Kuen-Feng Chen, Jung-Chen Su, Chun-Yu Liu, Jui-Wen Huang, Kuei-Chiu Chen, Wei-Lin Chen, Wei-Tien Tai, Chung-Wai Shiau,