دورية أكاديمية

Antiproliferative effects of cinobufacini on human hepatocellular carcinoma HepG2 cells detected by atomic force microscopy.

التفاصيل البيبلوغرافية
العنوان: Antiproliferative effects of cinobufacini on human hepatocellular carcinoma HepG2 cells detected by atomic force microscopy.
المؤلفون: Wu Q; Qing Wu, Wei-Dong Lin, Guan-Qun Liao, Li-Guo Zhang, Shun-Qian Wen, Jia-Ying Lin, Department of General Surgery, the Affiliated Foshan Hospital of Southern Medical University, Foshan 528000, Guangdong Province, China., Lin WD; Qing Wu, Wei-Dong Lin, Guan-Qun Liao, Li-Guo Zhang, Shun-Qian Wen, Jia-Ying Lin, Department of General Surgery, the Affiliated Foshan Hospital of Southern Medical University, Foshan 528000, Guangdong Province, China., Liao GQ; Qing Wu, Wei-Dong Lin, Guan-Qun Liao, Li-Guo Zhang, Shun-Qian Wen, Jia-Ying Lin, Department of General Surgery, the Affiliated Foshan Hospital of Southern Medical University, Foshan 528000, Guangdong Province, China., Zhang LG; Qing Wu, Wei-Dong Lin, Guan-Qun Liao, Li-Guo Zhang, Shun-Qian Wen, Jia-Ying Lin, Department of General Surgery, the Affiliated Foshan Hospital of Southern Medical University, Foshan 528000, Guangdong Province, China., Wen SQ; Qing Wu, Wei-Dong Lin, Guan-Qun Liao, Li-Guo Zhang, Shun-Qian Wen, Jia-Ying Lin, Department of General Surgery, the Affiliated Foshan Hospital of Southern Medical University, Foshan 528000, Guangdong Province, China., Lin JY; Qing Wu, Wei-Dong Lin, Guan-Qun Liao, Li-Guo Zhang, Shun-Qian Wen, Jia-Ying Lin, Department of General Surgery, the Affiliated Foshan Hospital of Southern Medical University, Foshan 528000, Guangdong Province, China.
المصدر: World journal of gastroenterology [World J Gastroenterol] 2015 Jan 21; Vol. 21 (3), pp. 854-61.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Baishideng Publishing Group Country of Publication: United States NLM ID: 100883448 Publication Model: Print Cited Medium: Internet ISSN: 2219-2840 (Electronic) Linking ISSN: 10079327 NLM ISO Abbreviation: World J Gastroenterol Subsets: MEDLINE
أسماء مطبوعة: Publication: 2014- : Pleasanton, CA : Baishideng Publishing Group
Original Publication: Beijing : WJG Press, c1998-
مواضيع طبية MeSH: Microscopy, Atomic Force*, Amphibian Venoms/*pharmacology , Antineoplastic Agents/*pharmacology , Carcinoma, Hepatocellular/*ultrastructure , Cell Proliferation/*drug effects , Liver Neoplasms/*ultrastructure, Actin Cytoskeleton/drug effects ; Actin Cytoskeleton/ultrastructure ; Cell Nucleus/drug effects ; Cell Nucleus/ultrastructure ; Cell Shape/drug effects ; Cell Survival/drug effects ; Dose-Response Relationship, Drug ; Flow Cytometry ; Hep G2 Cells ; Humans ; Microscopy, Confocal ; S Phase Cell Cycle Checkpoints/drug effects
مستخلص: Aim: To investigate the antiproliferative activity of cinobufacini on human hepatocellular carcinoma HepG2 cells and the possible mechanism of its action.
Methods: HepG2 cells were treated with different concentrations of cinobufacini. Cell viability was measured by methylthiazolyl tetrazolium (MTT) assay. Cell cycle distribution was analyzed by flow cytometry (FCM). Cytoskeletal and nuclear alterations were observed by fluorescein isothiocyanate-phalloidin and DAPI staining under a laser scanning confocal microscope. Changes in morphology and ultrastructure of cells were detected by atomic force microscopy (AFM) at the nanoscale level.
Results: MTT assay indicated that cinobufacini significantly inhibited the viability of HepG2 cells in a dose-dependent manner. With the concentration of cinobufacini increasing from 0 to 0.10 mg/mL, the cell viability decreased from 74.9% ± 2.7% to 49.41% ± 2.2% and 39.24% ± 2.1% (P < 0.05). FCM analysis demonstrated cell cycle arrest at S phase induced by cinobufacini. The immunofluorescence studies of cytoskeletal and nuclear morphology showed that after cinobufacini treatment, the regular reorganization of actin filaments in HepG2 cells become chaotic, while the nuclei were not damaged seriously. Additionally, high-resolution AFM imaging revealed that cell morphology and ultrastructure changed a lot after treatment with cinobufacini. It appeared as significant shrinkage and deep pores in the cell membrane, with larger particles and a rougher cell surface.
Conclusion: Cinobufacini inhibits the viability of HepG2 cells via cytoskeletal destruction and cell membrane toxicity.
References: Appl Microbiol Biotechnol. 2012 Feb;93(4):1715-23. (PMID: 22270235)
Bioorg Med Chem Lett. 2014 Jan 15;24(2):679-84. (PMID: 24365157)
Oncol Rep. 2012 May;27(5):1619-24. (PMID: 22267101)
PLoS One. 2012;7(1):e30066. (PMID: 22272274)
World J Gastroenterol. 2005 Mar 21;11(11):1709-11. (PMID: 15786556)
J Ethnopharmacol. 2012 Jun 1;141(2):692-700. (PMID: 22210051)
Eur J Pharmacol. 2011 Jan 10;650(1):41-7. (PMID: 20883687)
Scanning. 2013 Jul-Aug;35(4):253-60. (PMID: 23070725)
Biochim Biophys Acta. 2014 Mar;1840(3):1028-50. (PMID: 24291690)
Bioorg Med Chem Lett. 2012 Feb 1;22(3):1459-63. (PMID: 22225634)
Cancer. 2009 Nov 15;115(22):5309-18. (PMID: 19701908)
Nat Nanotechnol. 2009 Feb;4(2):72; author reply 72-3. (PMID: 19197298)
J Ethnopharmacol. 2010 Apr 21;128(3):654-61. (PMID: 20193751)
Appl Microbiol Biotechnol. 2013 Feb;97(3):1051-62. (PMID: 22945264)
Scanning. 2013 Sep-Oct;35(5):316-26. (PMID: 23239560)
Trends Cell Biol. 2011 Aug;21(8):461-9. (PMID: 21664134)
Biophys J. 1998 Aug;75(2):695-703. (PMID: 9675171)
Drug Discov Ther. 2008 Dec;2(6):339-43. (PMID: 22504743)
Biomed Res Int. 2014;2014:418624. (PMID: 24987682)
Biosens Bioelectron. 2009 Dec 15;25(4):721-7. (PMID: 19734031)
J Cell Biochem. 2011 Jan;112(1):169-78. (PMID: 21053362)
World J Gastroenterol. 2008 Sep 7;14(33):5210-6. (PMID: 18777599)
Scanning. 2013 Mar-Apr;35(2):119-26. (PMID: 22833475)
فهرسة مساهمة: Keywords: Atomic force microscopy; Cell viability; Cinobufacini; HepG2 cells; Hepatocarcinoma
المشرفين على المادة: 0 (Amphibian Venoms)
0 (Antineoplastic Agents)
0 (huachansu)
تواريخ الأحداث: Date Created: 20150128 Date Completed: 20150914 Latest Revision: 20181113
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC4299337
DOI: 10.3748/wjg.v21.i3.854
PMID: 25624718
قاعدة البيانات: MEDLINE
الوصف
تدمد:2219-2840
DOI:10.3748/wjg.v21.i3.854