Literature DB >> 21677689

SIRT1 RNAi knockdown induces apoptosis and senescence, inhibits invasion and enhances chemosensitivity in pancreatic cancer cells.

G Zhao1, J Cui, J-G Zhang, Q Qin, Q Chen, T Yin, S-C Deng, Y Liu, L Liu, B Wang, K Tian, G-B Wang, C-Y Wang.   

Abstract

The NAD(+)-dependent deacetylase, sirtuin 1 (SIRT1), has been recently been suspected to have a role in tumorigenesis. We investigated the expression of SIRT1 in pancreatic cancer and the effect of SIRT1-targeted RNA interference (RNAi) on cell proliferation and tumor formation in a pancreatic cancer cell line, PANC1. The expression of SIRT1 was investigated in 49 specimens of pancreatic cancer and adjacent normal pancreatic tissues. SIRT1 was overexpressed in pancreatic cancer tissues at both the mRNA and protein levels, with increased SIRT1 positivity associated with tumors from patients over 60 years old, tumors larger than 4 cm, higher TNM (extent of tumor (T), the extent of spread to lymph nodes (N), and presence of distant metastasis (M)) stage or the presence of lymph node or hepatic metastases. The PANC-1 was stably transfected with a SIRT1 small hairpin RNA (shRNA) expression plasmid and compared with untransfected and PANC-1-negative RNAi cells. Proliferation of PANC-1-SIRT1-RNAi cells was significantly reduced, accompanied by increased rates of apoptosis, G1 arrest and senescence. Furthermore, FOXO3a expression was markedly upregulated in PANC-1-SIRT1-RNAi cells, but no significant difference in p53 expression was observed. The invasive ability of PANC-1-SIRT1-RNAi cells was markedly reduced in vitro, which was linked to increased E-cadherin and reduced-MMP expression. Additionally, PANC-1-SIRT1-RNAi cells had a significantly reduced capacity to form tumors in vivo compared with untransfected and PANC-1-negative RNAi cells. These results suggest that SIRT1 may promote cell proliferation and tumor formation in pancreatic cancer, and downregulation of SIRT1 using shRNA could provide a novel therapeutic treatment.

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Year:  2011        PMID: 21677689     DOI: 10.1038/gt.2011.81

Source DB:  PubMed          Journal:  Gene Ther        ISSN: 0969-7128            Impact factor:   5.250


  49 in total

1.  SIRT1-Activating Compounds (STAC) Negatively Regulate Pancreatic Cancer Cell Growth and Viability Through a SIRT1 Lysosomal-Dependent Pathway.

Authors:  Claudia C S Chini; Jair M Espindola-Netto; Gourish Mondal; Anatilde M Gonzalez Guerrico; Veronica Nin; Carlos Escande; Mauro Sola-Penna; Jin-San Zhang; Daniel D Billadeau; Eduardo N Chini
Journal:  Clin Cancer Res       Date:  2015-12-11       Impact factor: 12.531

Review 2.  Circadian rhythm connections to oxidative stress: implications for human health.

Authors:  Melissa Wilking; Mary Ndiaye; Hasan Mukhtar; Nihal Ahmad
Journal:  Antioxid Redox Signal       Date:  2013-04-24       Impact factor: 8.401

3.  SIRT1 deacetylase is overexpressed in human melanoma and its small molecule inhibition imparts anti-proliferative response via p53 activation.

Authors:  Melissa J Wilking; Chandra Singh; Minakshi Nihal; Weixiong Zhong; Nihal Ahmad
Journal:  Arch Biochem Biophys       Date:  2014-04-18       Impact factor: 4.013

4.  The expression and correlation of SIRT1 and Phospho-SIRT1 in colorectal cancer.

Authors:  Xianzhen Zhang; Suiqin Chen; Meili Cheng; Fangli Cao; Yufeng Cheng
Journal:  Int J Clin Exp Med       Date:  2015-01-15

5.  p53 and miR-34a Feedback Promotes Lung Epithelial Injury and Pulmonary Fibrosis.

Authors:  Shwetha K Shetty; Nivedita Tiwari; Amarnath S Marudamuthu; Bijesh Puthusseri; Yashodhar P Bhandary; Jian Fu; Jeffrey Levin; Steven Idell; Sreerama Shetty
Journal:  Am J Pathol       Date:  2017-03-06       Impact factor: 4.307

Review 6.  Mechanistic understanding of β-cryptoxanthin and lycopene in cancer prevention in animal models.

Authors:  Ji Ye Lim; Xiang-Dong Wang
Journal:  Biochim Biophys Acta Mol Cell Biol Lipids       Date:  2020-02-05       Impact factor: 4.698

7.  Ectopic expression of miR-494 inhibited the proliferation, invasion and chemoresistance of pancreatic cancer by regulating SIRT1 and c-Myc.

Authors:  Y Liu; X Li; S Zhu; J-g Zhang; M Yang; Q Qin; S-c Deng; B Wang; K Tian; L Liu; Y Niu; C-y Wang; G Zhao
Journal:  Gene Ther       Date:  2015-04-28       Impact factor: 5.250

8.  Effects of gambogic acid on the activation of caspase-3 and downregulation of SIRT1 in RPMI-8226 multiple myeloma cells via the accumulation of ROS.

Authors:  Li-Jing Yang; Yan Chen; Jing He; Sha Yi; Lu Wen; Shuai Zhao; Guo-Hui Cui
Journal:  Oncol Lett       Date:  2012-03-06       Impact factor: 2.967

9.  Clinicopathological significance of SIRT1 expression in colorectal adenocarcinoma.

Authors:  Liang Lv; Zhanlong Shen; Jizhun Zhang; Hui Zhang; Jianqiang Dong; Yichao Yan; Fangfang Liu; Kewei Jiang; Yingjiang Ye; Shan Wang
Journal:  Med Oncol       Date:  2014-05-10       Impact factor: 3.064

Review 10.  Metabolism, longevity and epigenetics.

Authors:  Claudia Cosentino; Raul Mostoslavsky
Journal:  Cell Mol Life Sci       Date:  2013-03-07       Impact factor: 9.261

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