1 microrna silencing of tumor suppressor dlc-1 promotes efficient hepatitis c virus replication in...

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1 MicroRNA Silencing of Tumor Sup pressor DLC-1 Promotes Efficien t Hepatitis C Virus Replication in Primary Human Hepatocytes 指指指指 指指指指指指 指指指指指 :、 指指 指指指 (N99H0005) 指指指指 :2011/05/01 HEPATOLOGY, 2011;53:53- 61

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Page 1: 1 MicroRNA Silencing of Tumor Suppressor DLC-1 Promotes Efficient Hepatitis C Virus Replication in Primary Human Hepatocytes 指導老師:鄭伯智老師、林宏榮老師 學生:林怡君

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MicroRNA Silencing of Tumor Suppressor DLC-1 Promotes Efficient Hepatitis C Virus Replication in Primary Human Hepatocytes

指導老師:鄭伯智老師、林宏榮老師學生:林怡君 (N99H0005)報告日期 :2011/05/01

HEPATOLOGY, 2011;53:53-61

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IntroductionIntroduction

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MicroRNA (miRNAs)

The first miRNA, lin-4, was identified in 1993 in a genetic screen for mutants that disrupt the timing of post-embryonic development in Caenorhabditis elegans (Lee et al., 1993).

miRNAs are approximately 22-nucleotide noncoding RNAs that constitute silencers of target gene expression.

Development 132, 4645-4652

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5Development, 2005

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Deregulated cell proliferation and apoptosis play a major role in hepatocellular carcinoma (HCC). MicroRNAs participate in the modulation of key molecules linked to hepatocarcinogenesis.

Clin Cancer Res 2009;15(16):5073–81

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Hepatitis C Virus (HCV)

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Pathology of HCV

Acute Hepatitis C:Generally benign:

No jaundice (80%)Usually asymptomatic

Can be severe, but liver failure rare

Only real threat of acute Hepatitis C is its ability to reach chronic stages undetected and untreated.

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Pathology of HCV Chronic Hepatitis C:

70% of patients become chronic Possible results:

Cirrhosis End-stage liver disease Hepatocellular carcinoma

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The gene deleted in liver cancer-1 (DLC-1) is located on human chromosome 8p21–22, a region thought to harbor tumor suppressor genes on the basis of its frequent deletion or loss of heterozygosity in a variety of human cancers, including hepatocellular carcinoma (HCC).

Oncogene (2004) 23, 1308–1313

Deleted in Liver Cancer-1 (DLC-1)

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Chronic Hepatitis C

Cancer

DLC-1Induce

Infected cellapoptosis

MiRNA

HCV

HCV

?

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Materials and MethodsMaterials and Methods

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Primary Hepatocyte Coculture

RNA-Primed, Array-Based Klenow Enzyme Assay

Luciferase Reporter Assay

Western Blot Analysis

Reverse-Transcription, and QuantitativePCR

Flow Cytometry of Ki67 Nuclear Antigen FluorescenceStained

HCV 1a 、 1b 、 2a infection

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NATURE METHODS | VOL.1 NO.2 | NOVEMBER 2004

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Luciferase Reporter Assay

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ResultsResults

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Fig. 1. Changes in miRNAs in HCV-infected primary hepatocytes. Array-based Klenow extension profiles are shown for pairwise comparison of uninfected hepatocyte miRNAs with hepatocytes infected with HCV genotype 1a (A), genotype 1b (B), or genotype 2a (C).

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Fig. 2. Changes in miR-141 and miR-200a upon HCV infection of hepatocytes.

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Summary-1

cells infected with the HCV strains showed induced expression of miR-141, miR-200a, and miR-200b and miR-200c.

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Fig. 3. Inhibition of DLC-1 expression by miR-141 induced in HCV infected hepatocytes.

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Summary-2

The results suggest that DLC-1 expression in HCV1a-infected cells is regulated by intracellular miR-141.

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Fig. 4. DLC-1 protein level is reduced in cells with replicating HCV.

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Fig. 5. Changes in DLC1 protein levels in response to miR-141 in uninfected and HCV1a-infected cells.

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Fig. 6. (A) Effects of miR-141 on HCV RNA replication. (B) Effects of miR-141 on the release of mature HCV particles from infected cells.

+--

+-+

++-

+--

+-+

++-

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Fig. 6.(C) Effects of miR-141 on DLC-1 mRNA.

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Summary- 3

HCV replication in infected hepatocytes relies on miR-141–mediated depletion of tumor suppressor DLC-1.

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Fig. 7. (A) Immunostaining of Ki67 nuclear antigen with fluorescein isothiocyanate. (B) Quantitation of Ki67-positive cells.

Uninfected control HCV 1a infection DLC-1+HCV 1a infection

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Fig. 7.(C) Quantitation of Ki67-positive cells by flow cytometry.

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Summary- 4

The results showed an approximately 40% increase in cell proliferation of HCV1a-infected hepatocytes.

The increased cell proliferation is neutralized when the DLC-1 level was artificially increased through transfection with a DLC-1 expression vector.

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Discussion

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Efficient HCV replication is correlated with miR-141–mediated reduction of DLC-1 protein in virus infected cells.

The exact mechanism by which miR-141 or DLC-1 modulate virus replication is not clear.

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ConclusionConclusion

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Chronic Hepatitis C

Cancer

InduceInfected cellapoptosis

MiRNA

HCV

HCV

DLC-1

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Thanks for your attention!!Thanks for your attention!!

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Examples of miRNA Functions & Relevance of miRNA to Human Biology

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Development 132, 4645-4652

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49Nature Biotechnology 25, 631 - 638 (2007)

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HCV Structure

RNA virus Single-stranded Positive-sense 9400 nucleotide

Virion: Enveloped Icosahedral capsid 40-60 nm in diameter

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Part of Flaviviridae family of viruses Associated with both human and animal disease 3 genera: pestiviruses (cattle, pigs), flaviviruses (dengue,

yellow fever), hepaciviruses (HCV) In hepacivirus family:

6 major clades >100 different subtypes

Countless quasispecies: mult. seen in each infected individual

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HCV Life Cycle

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The origin of MicroRNA : 1.Extronic miRNA in non-coding transcription units1.Intronic miRNA in non-coding transcription units.2.Intronic miRNA in protein-coding transcription units