دورية أكاديمية

Effects of CS-1 on A431 cell proliferation, cell cycle, and epidermal growth factor receptor signal transduction

التفاصيل البيبلوغرافية
العنوان: Effects of CS-1 on A431 cell proliferation, cell cycle, and epidermal growth factor receptor signal transduction
المؤلفون: Du, Haiyan, Xu, Bo, Wu, Caixia, Li, Min, Ran, Fuxiang, Cai, Shaoqing, Cui, Jingrong
المساهمون: Cui, JR (reprint author), Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China., Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China., Capital Med Univ, Drug Clin Trail Inst, Beijing Anzhen Hosp, Beijing 100029, Peoples R China., Shandong Med Coll, Linyi 276000, Peoples R China., Peking Univ, Dept Nat Med, Sch Pharmaceut Sci, Beijing 100191, Peoples R China.
المصدر: PubMed ; SCI
بيانات النشر: acta biochimica et biophysica sinica
سنة النشر: 2012
المجموعة: Peking University Institutional Repository (PKU IR) / 北京大学机构知识库
مصطلحات موضوعية: CS-1, cell cycle, EGFR signaling pathway, high content screening, NASOPHARYNGEAL CARCINOMA-CELLS, KINASE, INHIBITION, ACTIVATION, EXPRESSION
الوصف: CS-1, a new alkaloid with a molecular formula of C21H20O8N2S, is extracted from traditional Chinese medicine. Previous studies have shown that CS-1 can inhibit the proliferation of several human carcinoma cells in vivo and in vitro. The aims of this study are to investigate the anti-tumor effect and mechanism of CS-1 in epidermal growth factor receptor (EGFR) signaling pathway in human A431 cell line. Through the sulforhodamine B assay, we found that CS-1 inhibited A431 cell proliferation in the concentration- and time-dependent manners. The inhibitory rate ranged from 14.5% to 87.8% after 24 h of incubation. High content screening (HCS) multi-parameters cytotoxicity analysis showed that CS-1 at high concentration had slight cytotoxicity that resulted from the cell permeabilization and slight reduction in total mitochondrial mass, whereas no change in nucleus size/morphology and lysosomal mass-pH was found. The cytotoxicity of CS-1 was not a major reason for its anti-proliferative effect. Cell cycle analysis indicated that CS-1 induced G1-phase arrest in A431 cells in a time-dependent manner at high concentration (2.5 mu M), and S-phase arrest at low concentration (0.625 mu M). The HCS assay also showed that CS-1 could inhibit the EGFR internalization, extracellular-signal-regulated kinase (Erk)/mitogen-activated protein kinase translocation to nucleus, the accumulation of phosphorylated protein kinase B (Akt), signal transducer and activator of transcription 3 (STAT3), and cyclin D1 in the nucleus. These results were confirmed by the western blot analysis. CS-1 might inhibit the epidermal growth factor binding to its receptor, resulting in the inhibition of the accumulation of phosphorylated Erk and Akt, and STAT3 in the nucleus, and affecting the transcription of cyclin D1 and cell cycle arrest in G1/S phase. ...
نوع الوثيقة: journal/newspaper
اللغة: English
تدمد: 1672-9145
العلاقة: ACTA BIOCHIMICA ET BIOPHYSICA SINICA.2012,44,(2),136-146.; 661465; http://hdl.handle.net/20.500.11897/323061Test; WOS:000299744000005
DOI: 10.1093/abbs/gmr111
الإتاحة: https://doi.org/20.500.11897/323061Test
https://doi.org/10.1093/abbs/gmr111Test
https://hdl.handle.net/20.500.11897/323061Test
رقم الانضمام: edsbas.B85C1BCD
قاعدة البيانات: BASE
الوصف
تدمد:16729145
DOI:10.1093/abbs/gmr111