Menu utilisateur

Accès à distance ? S'identifier sur le proxy UCLouvain

microRNA-155, Induced by Interleukin-1ß, Represses the Expression of Microphthalmia-Associated Transcription Factor (MITF-M) in Melanoma Cells

  • Open access
  • PDF
  • 3.40 M
  1. Shibahara Shigeki, Takeda Kazuhisa, Yasumoto Ken-ichi, Udono Tetsuo, Watanabe Ken-ichi, Saito Hideo, Takahashi Kazuhiro, Microphthalmia-Associated Transcription Factor (MITF): Multiplicity in Structure, Function, and Regulation, 10.1046/j.0022-202x.2001.00010.x
  2. Vance Keith W., Goding Colin R., The Transcription Network Regulating Melanocyte Development and Melanoma, 10.1111/j.1600-0749.2004.00164.x
  3. Brichard V., The tyrosinase gene codes for an antigen recognized by autologous cytolytic T lymphocytes on HLA-A2 melanomas, 10.1084/jem.178.2.489
  4. Coulie P. G., A new gene coding for a differentiation antigen recognized by autologous cytolytic T lymphocytes on HLA-A2 melanomas, 10.1084/jem.180.1.35
  5. Zarour Hassane, Smet Charles De, Lehmann Frédéric, Marchand Marie, Lethé Bernard, Romero Pedro, Boon Thierry, Renauld Jean-Christophe, The Majority of Autologous Cytolytic T-Lymphocyte Clones Derived from Peripheral Blood Lymphocytes of a Melanoma Patient Recognize an Antigenic Peptide Derived from Gene Pmel17/gp100, 10.1111/1523-1747.ep12298177
  6. Romero Pedro, Valmori Danila, Pittet Mikael J., Zippelius Alfred, Rimoldi Donata, Levy Frederic, Dutoit Valerie, Ayyoub Maha, Rubio-Godoy Verena, Michielin Olivier, Guillaume Philippe, Batard Pascal, Luescher Immanuel F., Lejeune Ferdy, Lienard Danielle, Rufer Nathalie, Dietrich Pierre-Yves, Speiser Daniel E., Cerottini Jean-Charles, Antigenicity and immunogenicity of Melan-A/MART-1 derived peptides as targets for tumor reactive CTL in human melanoma, 10.1034/j.1600-065x.2002.18808.x
  7. V Voelter, Cancer immunity, 8, 6 (2008)
  8. Boon Thierry, Coulie Pierre G., Eynde Benoît J. Van den, Bruggen Pierre van der, HUMAN T CELL RESPONSES AGAINST MELANOMA, 10.1146/annurev.immunol.24.021605.090733
  9. Gallimore Awen, Godkin Andrew, Regulatory T cells and tumour immunity - observations in mice and men : Regulatory T cells and tumour immunity, 10.1111/j.1365-2567.2007.02748.x
  10. Uyttenhove Catherine, Pilotte Luc, Théate Ivan, Stroobant Vincent, Colau Didier, Parmentier Nicolas, Boon Thierry, Van den Eynde Benoît J, Evidence for a tumoral immune resistance mechanism based on tryptophan degradation by indoleamine 2,3-dioxygenase, 10.1038/nm934
  11. Pilotte L., Larrieu P., Stroobant V., Colau D., Dolusic E., Frederick R., De Plaen E., Uyttenhove C., Wouters J., Masereel B., Van den Eynde B. J., Reversal of tumoral immune resistance by inhibition of tryptophan 2,3-dioxygenase, 10.1073/pnas.1113873109
  12. Landskron Glauben, De la Fuente Marjorie, Thuwajit Peti, Thuwajit Chanitra, Hermoso Marcela A., Chronic Inflammation and Cytokines in the Tumor Microenvironment, 10.1155/2014/149185
  13. Le Poole I. Caroline, Riker Adam I., Quevedo M. Eugenia, Stennett Lawrence S., Wang Ena, Marincola Francesco M., Kast W. Martin, Robinson June K., Nickoloff Brian J., Interferon-γ Reduces Melanosomal Antigen Expression and Recognition of Melanoma Cells by Cytotoxic T Cells, 10.1016/s0002-9440(10)64871-7
  14. DJ Schwartzentruber, Journal of immunology, 146, 3674 (1991)
  15. Englaro Walter, Bahadoran Philippe, Bertolotto Corine, Buscà Roser, Dérijard Benoit, Livolsi Antonia, Peyron Jean-François, Ortonne Jean-Paul, Ballotti Robert, Tumor necrosis factor alpha-mediated inhibition of melanogenesis is dependent on nuclear factor kappa B activation, 10.1038/sj.onc.1202446
  16. Landsberg Jennifer, Kohlmeyer Judith, Renn Marcel, Bald Tobias, Rogava Meri, Cron Mira, Fatho Martina, Lennerz Volker, Wölfel Thomas, Hölzel Michael, Tüting Thomas, Melanomas resist T-cell therapy through inflammation-induced reversible dedifferentiation, 10.1038/nature11538
  17. JL Bennicelli, Cancer research, 49, 930 (1989)
  18. DM Elaraj, American Association for Cancer Research, 12, 1088 (2006)
  19. Kholmanskikh Olga, van Baren Nicolas, Brasseur Francis, Ottaviani Sabrina, Vanacker Julie, Arts Nathalie, van der Bruggen Pierre, Coulie Pierre, De Plaen Etienne, Interleukins 1α and 1β secreted by some melanoma cell lines strongly reduce expression of MITF-M and melanocyte differentiation antigens, 10.1002/ijc.25182
  20. Houghton A. N., Phenotypic heterogeneity of melanoma. Relation to the differentiation program of melanoma cells, 10.1084/jem.165.3.812
  21. Huijbers Ivo J., Krimpenfort Paul, Chomez Patrick, van der Valk Martin A., Song Ji-Ying, Inderberg-Suso Else-Marit, Schmitt-Verhulst Anne-Marie, Berns Anton, Van den Eynde Benoît J., An Inducible Mouse Model of Melanoma Expressing a Defined Tumor Antigen, 10.1158/0008-5472.can-05-3216
  22. Bemis L. T., Chen R., Amato C. M., Classen E. H., Robinson S. E., Coffey D. G., Erickson P. F., Shellman Y. G., Robinson W. A., MicroRNA-137 Targets Microphthalmia-Associated Transcription Factor in Melanoma Cell Lines, 10.1158/0008-5472.can-07-2912
  23. Haflidadóttir Benedikta S., Bergsteinsdóttir Kristín, Praetorius Christian, Steingrímsson Eiríkur, miR-148 Regulates Mitf in Melanoma Cells, 10.1371/journal.pone.0011574
  24. Goswami Srikanta, Tarapore Rohinton S., TeSlaa Jessica J., Grinblat Yevgenya, Setaluri Vijayasaradhi, Spiegelman Vladimir S., MicroRNA-340-mediated Degradation of Microphthalmia-associated Transcription Factor mRNA Is Inhibited by the Coding Region Determinant-binding Protein, 10.1074/jbc.m110.109298
  25. Xu Shunbin, Witmer P. Dane, Lumayag Stephen, Kovacs Beatrix, Valle David, MicroRNA (miRNA) Transcriptome of Mouse Retina and Identification of a Sensory Organ-specific miRNA Cluster, 10.1074/jbc.m700501200
  26. Mann M., Barad O., Agami R., Geiger B., Hornstein E., miRNA-based mechanism for the commitment of multipotent progenitors to a single cellular fate, 10.1073/pnas.0915022107
  27. Yin Qinyan, Wang Xia, McBride Jane, Fewell Claire, Flemington Erik, B-cell Receptor Activation Induces BIC/miR-155 Expression through a Conserved AP-1 Element, 10.1074/jbc.m708218200
  28. Gauthy Emilie, Cuende Julia, Stockis Julie, Huygens Caroline, Lethé Bernard, Collet Jean-François, Bommer Guido, Coulie Pierre G., Lucas Sophie, GARP Is Regulated by miRNAs and Controls Latent TGF-β1 Production by Human Regulatory T Cells, 10.1371/journal.pone.0076186
  29. Bondurand N., Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome, 10.1093/hmg/9.13.1907
  30. Steingrímsson Eiríkur, Copeland Neal G., Jenkins Nancy A., Melanocytes and theMicrophthalmiaTranscription Factor Network, 10.1146/annurev.genet.38.072902.092717
  31. Watanabe Ken-ichi, Takeda Kazuhisa, Yasumoto Ken-ichi, Udono Tetsuo, Saito Hideo, Ikeda Katsuhisa, Takasaka Tomonori, Takahashi Kazuhiro, Kobayashi Toshimitsu, Tachibana Masayoshi, Shibahara Shigeki, Identification of a Distal Enhancer for the Melanocyte-Specific Promoter of the MITF Gene, 10.1034/j.1600-0749.2002.01080.x
  32. Soudja S. M., Wehbe M., Mas A., Chasson L., de Tenbossche C. P., Huijbers I., Van den Eynde B., Schmitt-Verhulst A. M., Tumor-Initiated Inflammation Overrides Protective Adaptive Immunity in an Induced Melanoma Model in Mice, 10.1158/0008-5472.can-09-4354
  33. Thomas Aaron J., Erickson Carol A., The making of a melanocyte: the specification of melanoblasts from the neural crest, 10.1111/j.1755-148x.2008.00506.x
  34. Hoek Keith S., Goding Colin R., Cancer stem cells versus phenotype-switching in melanoma : Phenotype-switching in melanoma, 10.1111/j.1755-148x.2010.00757.x
  35. Nishimura Emi K., Suzuki Misa, Igras Vivien, Du Jinyan, Lonning Scott, Miyachi Yoshiki, Roes Jürgen, Beermann Friedrich, Fisher David E., Key Roles for Transforming Growth Factor β in Melanocyte Stem Cell Maintenance, 10.1016/j.stem.2009.12.010
  36. Pierrat Marie-Jeanne, Marsaud Véronique, Mauviel Alain, Javelaud Delphine, Expression of Microphthalmia-associated Transcription Factor (MITF), Which Is Critical for Melanoma Progression, Is Inhibited by Both Transcription Factor GLI2 and Transforming Growth Factor-β, 10.1074/jbc.m112.358341
  37. Kong W., Yang H., He L., Zhao J.-j., Coppola D., Dalton W. S., Cheng J. Q., MicroRNA-155 Is Regulated by the Transforming Growth Factor  /Smad Pathway and Contributes to Epithelial Cell Plasticity by Targeting RhoA, 10.1128/mcb.00941-08
  38. Swope Viki B, Abdel-Malek Zalfa, Kassem Lina M, Nordlund James J, Interleukins 1α and 6 and Tumor Necrosis Factor-α Are Paracrine Inhibitors of Human Melanocyte Proliferation and Melanogenesis, 10.1111/1523-1747.ep12460991
  39. Bell Rachel E., Levy Carmit, The three M’s: melanoma, microphthalmia-associated transcription factor and microRNA : The three M’s: melanoma, MITF and microRNA, 10.1111/j.1755-148x.2011.00931.x
  40. Hoek K. S., Eichhoff O. M., Schlegel N. C., Dobbeling U., Kobert N., Schaerer L., Hemmi S., Dummer R., In vivo Switching of Human Melanoma Cells between Proliferative and Invasive States, 10.1158/0008-5472.can-07-2491
  41. Cheli Y, Guiliano S, Botton T, Rocchi S, Hofman V, Hofman P, Bahadoran P, Bertolotto C, Ballotti R, Mitf is the key molecular switch between mouse or human melanoma initiating cells and their differentiated progeny, 10.1038/onc.2010.598
  42. Sáez-Ayala Magalí, Montenegro María F., Sánchez-del-Campo Luis, Fernández-Pérez María Piedad, Chazarra Soledad, Freter Rasmus, Middleton Mark, Piñero-Madrona Antonio, Cabezas-Herrera Juan, Goding Colin R., Rodríguez-López José Neptuno, Directed Phenotype Switching as an Effective Antimelanoma Strategy, 10.1016/j.ccr.2013.05.009
Référence bibliographique Arts, Nathalie ; Cané, Stefania ; Hennequart, Marc ; Lamy, Juliette ; Bommer, Guido ; et. al. microRNA-155, Induced by Interleukin-1ß, Represses the Expression of Microphthalmia-Associated Transcription Factor (MITF-M) in Melanoma Cells. In: PLoS One, Vol. 10, no.4, p. e0122517 (08/04/2015)
Permalien http://hdl.handle.net/2078.1/158669