MiR-192 inhibits nucleotide excision repair by targeting ERCC3 and ERCC4 in HepG2.2.15 cells

Biochemical and Biophysical Research Communications

Volumn 410, Issue 3, 2011, Pages 440-445

  Xie, Qiong Hui ^a   He, Xing Xing ^a   Chang, Ying ^a   Sun, Shu zhen ^a   Jiang, Xiang ^a   Li, Pei Yuan ^a   Lin, Ju Sheng ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

ERCC3; ERCC4; MiR 192; Nucleotide excision repair

Indexed keywords

EXCISION REPAIR CROSS COMPLEMENTING PROTEIN 3; EXCISION REPAIR CROSS COMPLEMENTING PROTEIN 4; MICRORNA; NUCLEIC ACID BINDING PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CELL STRAIN HEPG2; EXCISION REPAIR; GENE CONTROL; GENE EXPRESSION; HEPATITIS B; PRIORITY JOURNAL; PROTEIN EXPRESSION; UPREGULATION;

CELL LINE, TUMOR; DNA HELICASES; DNA REPAIR; DNA-BINDING PROTEINS; GENOMIC INSTABILITY; HELA CELLS; HEPATITIS B VIRUS; HEPATITIS B, CHRONIC; HUMANS; MICRORNAS;

HEPATITIS B VIRUS;

EID: 79960034688     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2011.05.153     Document Type: Article

References (30)

1. Natarajan A.T., Palitti F. DNA repair and chromosomal alterations. Mutat. Res. 2008, 657:3-7.
2. Nouspikel T. DNA repair in mammalian cells: nucleotide excision repair: variations on versatility. Cell Mol. Life Sci. 2009, 66:994-1009.
3. van Pelt J.F., Severi T., Crabbe T., Eetveldt A.V., Verslype C., Roskams T., Fevery J. Expression of hepatitis C virus core protein impairs DNA repair in human hepatoma cells. Cancer Lett. 2004, 209:197-205.
4. Schavinsky-Khrapunsky Y., Priel E., Aboud M. Dose-dependent dual effect of HTLV-1 tax oncoprotein on p53-dependent nucleotide excision repair in human T-cells. Int. J. Cancer 2008, 122:305-316.
5. Matsuda Y., Ichida T. Impact of hepatitis B virus X protein on the DNA damage response during hepatocarcinogenesis. Med. Mol. Morphol. 2009, 42:138-142.
6. Lee A.T., Ren J., Wong E.T., Ban K.H., Lee L.A., Lee C.G. The hepatitis B virus X protein sensitizes HepG2 cells to UV light-induced DNA damage. J. Biol. Chem. 2005, 280:33525-33535.
7. Bartel D.P. MicroRNAs:genomics biogenesis mechanism and function. Cell 2004, 116:281-297.
8. Hu H., Gatti R.A. MicroRNAs: new players in the DNA damage response. J. Mol. Cell Biol. 2010.
9. Crosby M.E., Kulshreshtha R., Ivan M., Glazer P.M. MicroRNA regulation of DNA repair gene expression in hypoxic stress. Cancer Res. 2009, 69:1221-1229.
10. Yan D., Ng W.L., Zhang X., Wang P., Zhang Z., Mo Y.Y., Mao H., Hao C., Olson J.J., Curran W.J., Wang Y. Targeting DNA-PKcs and ATM with miR-101 sensitizes tumors to radiation. PLoS One 2010, 5:e11397.
11. Georges S.A., Biery M.C., Kim S.Y., Schelter J.M., Guo J., Chang A.N., Jackson A.L., Carleton M.O., Linsley P.S., Cleary M.A., Chau B.N., microRNAs Coordinated regulation of cell cycle transcripts by p53-Inducible miR-192 and miR-215. Cancer Res. 2008, 68:10105-10112.
12. Sells M.A., Chen M.L., Acs G. Production of hepatitis B virus particles in Hep G2 cells transfected with cloned hepatitis B virus DNA. Proc. Natl. Acad. Sci. USA 1987, 84:1005-1009.
13. He X.X., Chen T., Lin J.S., Chang Y., Ye B.X., 2 Inhibition of the replication of hepatitis B virus in vitro by a novel, analog 6-diaminopurine beta-LPA. Biochem. Biophys. Res. Commun. 2008, 369:513-518.
14. Feng Z., Hu W., Tang M.S. Trans-4-hydroxy-2-nonenal inhibits nucleotide excision repair in human cells: a possible mechanism for lipid peroxidation-induced carcinogenesis. Proc. Natl. Acad. Sci. USA 2004, 101:8598-8602.
15. Wang K., Zhang S., Marzolf B., Troisch P., Brightman A., Hu Z., Hood L.E., Galas D.J., microRNAs Circulating potential biomarkers for drug-induced liver injury. Proc. Natl. Acad. Sci. USA 2009, 106:4402-4407.
16. Kremsdorf D., Soussan P., Paterlini-Brechot P., Brechot C. Hepatitis B virus-related hepatocellular carcinoma: paradigms for viral-related human carcinogenesis. Oncogene 2006, 25:3823-3833.
17. Yu M.C., Yuan J.M. Environmental factors and risk for hepatocellular carcinoma. Gastroenterology 2004, 127:S72-78.
18. Alekseyev Y.O., Hamm M.L., Essigmann J.M. Aflatoxin B1 formamidopyrimidine adducts are preferentially repaired by the nucleotide excision repair pathway in vivo. Carcinogenesis 2004, 25:1045-1051.
19. Ming L., Thorgeirsson S.S., Gail M.H., Lu P., Harris C.C., Wang N., Shao Y., Wu Z., Liu G., Wang X., Sun Z., virus Dominant role of hepatitis B, Qidong cofactor role of aflatoxin in hepatocarcinogenesis in China. Hepatology 2002, 36:1214-1220.
20. Nuovo G.J., Wu X., Volinia S., Yan F., di Leva G., Chin N., Nicol A.F., Jiang J., Otterson G., Schmittgen T.D., Croce C. Strong inverse correlation between microRNA-125b and human papillomavirus DNA in productive infection. Diagn. Mol. Pathol. 2010, 19:135-143.
21. Cameron J.E., Yin Q., Fewell C., Lacey M., McBride J., Wang X., Lin Z., Schaefer B.C., Flemington E.K., miR-146a Epstein-Barr virus latent membrane protein 1 induces cellular MicroRNA a modulator of lymphocyte signaling pathways. J. Virol. 2008, 82:1946-1958.
22. Hou J., Wang P., Lin L., Liu X., Ma F., An H., Wang Z., Cao X., TRAF6 MicroRNA-146a feedback inhibits RIG-I-dependent Type I IFN production in macrophages by targeting, IRAK1 and IRAK2. J. Immunol. 2009, 183:2150-2158.
23. Rom S., Rom I., Passiatore G., Pacifici M., Radhakrishnan S., Del Valle L., Pina-Oviedo S., Khalili K., Eletto D., Peruzzi F. CCL8/MCP-2 is a target for mir-146a in HIV-1-infected human microglial cells. FASEB J. 2010, 24:2292-2300.
24. Barad O., Meiri E., Avniel A., Aharonov R., Barzilai A., Bentwich I., Einav U., Gilad S., Hurban P., Karov Y., Lobenhofer E.K., Sharon E., Shiboleth Y.M., Shtutman M., Bentwich Z., Einat P. MicroRNA expression detected by oligonucleotide microarrays: system establishment and expression profiling in human tissues. Genome Res. 2004, 14:2486-2494.
25. Braun C.J., Zhang X., Savelyeva I., Wolff S., Moll U.M., Schepeler T., Orntoft T.F., Andersen C.L., Dobbelstein M. p53-Responsive micrornas 192 and 215 are capable of inducing cell cycle arrest. Cancer Res 2008, 68:10094-10104.
26. Chung A.C., Huang X.R., Meng X., Lan H.Y. miR-192 mediates TGF-beta/Smad3-driven renal fibrosis. J. Am. Soc. Nephrol. 2010, 21:1317-1325.
27. Lee D.K., Park S.H., Yi Y., Choi S.G., Lee C., Parks W.T., Cho H., de Caestecker M.P., Shaul Y., Roberts A.B., Kim S.J. The hepatitis B virus encoded oncoprotein pX amplifies TGF-beta family signaling through direct interaction with Smad4: potential mechanism of hepatitis B virus-induced liver fibrosis. Genes Dev. 2001, 15:455-466.
28. Hwang J.R., Moncollin V., Vermeulen W., Seroz T., van Vuuren H., Hoeijmakers J.H., Egly J.M., 3' A 5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription. J. Biol. Chem. 1996, 271:15898-15904.
29. Lankoff A., Sochacki J., Spoof L., Meriluoto J., Wojcik A., Wegierek A., Verschaeve L. Nucleotide excision repair impairment by nodularin in CHO cell lines due to ERCC1/XPF inactivation. Toxicol. Lett. 2008, 179:101-107.
30. van der Wees C., Jansen J., Vrieling H., van der Laarse A., Van Zeeland A., Mullenders L. Nucleotide excision repair in differentiated cells. Mutat. Res. 2007, 614:16-23.