Epigallocatechin-3-O-gallate up-regulates microRNA-let-7b expression by activating 67-kDa laminin receptor signaling in melanoma cells

Scientific Reports

Volumn 6, Issue , 2016, Pages

  Yamada, Shuhei ^a   Tsukamoto, Shuntaro ^a   Huang, Yuhui ^a   Makio, Akiko ^a   Kumazoe, Motofumi ^a   Yamashita, Shuya ^a   Tachibana, Hirofumi ^a  

^a KYUSHU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CATECHIN; CYCLIC AMP; CYCLIC AMP DEPENDENT PROTEIN KINASE; EPIGALLOCATECHIN GALLATE; HIGH MOBILITY GROUP A2 PROTEIN; LAMININ RECEPTOR; MICRORNA; MIRNLET7 MICRORNA, HUMAN; PHOSPHOPROTEIN PHOSPHATASE 2; RIBOSOME PROTEIN; RPSA PROTEIN, HUMAN;

ANALOGS AND DERIVATIVES; ANIMAL; DRUG EFFECTS; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENETICS; HUMAN; MELANOMA; METABOLISM; MOUSE; SIGNAL TRANSDUCTION; TUMOR CELL LINE;

ANIMALS; CATECHIN; CELL LINE, TUMOR; CYCLIC AMP; CYCLIC AMP-DEPENDENT PROTEIN KINASES; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, NEOPLASTIC; HMGA2 PROTEIN; HUMANS; MELANOMA; MICE; MICRORNAS; PROTEIN PHOSPHATASE 2; RECEPTORS, LAMININ; RIBOSOMAL PROTEINS; SIGNAL TRANSDUCTION;

EID: 84954456185     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep19225     Document Type: Article

References (34)

1. Ambros, V. microRNAs. Cell 107, 823-826 (2001).
2. Rathod, S. S., Rani, S. B., Khan, M., Muzumdar, D. & Shiras, A. Tumor suppressive miRNA-34a suppresses cell proliferation and tumor growth of glioma stem cells by targeting Akt and Wnt signaling pathways. FEBS Open Bio 4, 485-95 (2014).
3. Zhao, L. et al. MicroRNA-383 Regulates the Apoptosis of Tumor Cells through Targeting Gadd45g. PLoS One 9, e110472 (2014).
4. Rusca, N. et al. miR-146a and NF-B1 Regulate Mast Cell Survival and T Lymphocyte Differentiation. Mol. Cell. Biol. 32, 4432-4444 (2012).
5. Sun, X. et al. MicroRNA-181b regulates NF-κ B - mediated vascular inflammation. J Clin Invest 122, 1-18 (2012).
6. Kornfeld, J. W. et al. Obesity-induced overexpression of miR-802 impairs glucose metabolism through silencing of Hnf1b. Nature 494, 111-115 (2013).
7. Zou, Q., Li, J., Song, L., Zeng, X. & Wang, G. Similarity computation strategies in the microRNA-disease network: a survey. Brief. Funct. Genomics elv024; doi: 10.1093/bfgp/elv024 (2015).
8. Zou, Q. et al. Prediction of MicroRNA-Disease Associations Based on Social Network Analysis Methods. Biomed Res. Int. 2015, doi: 10.1155/20158/810514 (2015).
9. Lu, J. et al. MicroRNA expression profiles classify human cancers. Nature 435, 834-838 (2005).
10. Volinia, S. et al. A microRNA expression signature of human solid tumors defines cancer gene targets. Proc. Natl. Acad. Sci. USA 103, 2257-2261 (2006).
11. Parikh, A. et al. microRNA-181a has a critical role in ovarian cancer progression through the regulation of the epithelialmesenchymal transition. Nat. Commun. 5, 2977 (2014).
12. Yang, Y. et al. Downregulation of microRNA-21 expression restrains non-small cell lung cancer cell proliferation and migration through upregulation of programmed cell death 4. Cancer Gene Ther. 22, 23-29 (2014).
13. Yang, C. S., Wang, X., Lu, G. & Picinich, S. C. Cancer prevention by tea: animal studies, molecular mechanisms and human relevance. Nat. Rev. Cancer 9, 429-439 (2009).
14. Shammas, M.A. et al. Specific killing of multiple myeloma cells by (-)-epigallocatechin-3-gallate extracted from green tea: biologic activity and therapeutic implications. Blood 108, 2804-2810 (2006).
15. Shanafelt, T. D. et al. Phase 2 trial of daily, oral polyphenon e in patients with asymptomatic, Rai stage 0 to II chronic lymphocytic leukemia. Cancer 119, 363-370 (2013).
16. Bettuzzi, S. et al. Chemoprevention of human prostate cancer by oral administration of green tea catechins in volunteers with highgrade prostate intraepithelial neoplasia: A preliminary report from a one-year proof-of-principle study. Cancer Res. 66, 1234-1240 (2006).
17. Brausi, M., Rizzi, F. & Bettuzzi, S. Chemoprevention of Human Prostate Cancer by Green Tea Catechins: Two Years Later. A Followup Update. Eur. Urol. 54, 472-473 (2008).
18. Tachibana, H., Koga, K., Fujimura, Y. & Yamada, K. A receptor for green tea polyphenol EGCG. Nat. Struct. Mol. Biol. 11, 380-381 (2004).
19. Tachibana, H. Green tea polyphenol sensing. Proc. Japan Acad. Ser. B 87, 66-80 (2011).
20. Umeda, D., Yano, S., Yamada, K. & Tachibana, H. Green tea polyphenol epigallocatechin-3-gallate signaling pathway through 67-kDa laminin receptor. J. Biol. Chem. 283, 3050-3058 (2008).
21. Tsukamoto, S. et al. Green tea polyphenol EGCG induces lipid-raft clustering and apoptotic cell death by activating protein kinase Cδ and acid sphingomyelinase through a 67 kDa laminin receptor in multiple myeloma cells. Biochem. J. 443, 525-534 (2012).
22. Kumazoe, M. et al. 67-kDa laminin receptor increases cGMP to induce cancer-selective apoptosis. J. Clin. Invest. 123, 787-799 (2013).
23. Tsukamoto, S. et al. 67-kDa Laminin Receptor-dependent Protein Phosphatase 2A (PP2A) Activation Elicits Melanoma-specific Antitumor Activity Overcoming Drug Resistance. J. Biol. Chem. 289, 32671-32681 (2014).
24. Milenkovic, D. et al. Modulation of miRNA expression by dietary polyphenols in apoE deficient mice: A new mechanism of the action of polyphenols. PLoS One 7, e29837, doi: 10.1371/journal.pone.0029837 (2012).
25. Hui, C. et al. MicroRNA-34a and microRNA-21 play roles in the chemopreventive effects of 3,6-dihydroxyflavone on 1-methyl-1-nitrosourea-induced breast carcinogenesis. Breast Cancer Res. 14, R80 (2012).
26. Ohno, M. et al. The flavonoid apigenin improves glucose tolerance through inhibition of microRNA maturation in miRNA103 transgenic mice. Sci. Rep. 3, 2553 (2013).
27. Zhou, H. et al. Gene regulation mediated by microRNAs in response to green tea polyphenol EGCG in mouse lung cancer. BMC Genomics 15, S3 (2014).
28. Di Cello, F. et al. HMGA2 participates in transformation in human lung cancer. Mol. Cancer Res. 6, 743-750 (2008).
29. Liu, Q. et al. HMGA2 is down-regulated by microRNA let-7 and associated with epithelial-mesenchymal transition in oesophageal squamous cell carcinomas of Kazakhs. Histopathology 65, 408-417 (2014).
30. Johnson, S. M. et al. RAS is regulated by the let-7 microRNA family. Cell 120, 635-647 (2005).
31. Schultz, J., Lorenz, P., Gross, G., Ibrahim, S. & Kunz, M. MicroRNA let-7b targets important cell cycle molecules in malignant melanoma cells and interferes with anchorage-independent growth. Cell Res. 18, 549-557 (2008).
32. Perrotti, D. & Neviani, P. Protein phosphatase 2A: a target for anticancer therapy. Lancet Oncol 14, e229-e238 (2013).
33. Cristobal, I. et al. PP2A inhibition is a common event in colorectal cancer and its restoration using FTY720 shows promising therapeutic potential. Mol. Cancer Ther. 13, 938-947 (2014).
34. Winter, J., Jung, S., Keller, S., Gregory, R. I. & Diederichs, S. Many roads to maturity: microRNA biogenesis pathways and their regulation. Nat. Cell Biol. 11, 228-234 (2009).