User menu

Interleukins 1 alpha and 1 beta secreted by some melanoma cell lines strongly reduce expression of MITF-M and melanocyte differentiation antigens

Bibliographic reference Kholmanskikh, Olga ; van Baren, Nicolas ; Brasseur, Francis ; Ottaviani, Sabrina ; Vanacker, Julie ; et. al. Interleukins 1 alpha and 1 beta secreted by some melanoma cell lines strongly reduce expression of MITF-M and melanocyte differentiation antigens. In: International Journal of Cancer, Vol. 127, no. 7, p. 1625-36 (2010)
Permanent URL
  1. Rosenberg Steven A., Packard Beverly S., Aebersold Paul M., Solomon Diane, Topalian Suzanne L., Toy Stephen T., Simon Paul, Lotze Michael T., Yang James C., Seipp Claudia A., Simpson Colleen, Carter Charles, Bock Steven, Schwartzentruber Douglas, Wei John P., White Donald E., Use of Tumor-Infiltrating Lymphocytes and Interleukin-2 in the Immunotherapy of Patients with Metastatic Melanoma, 10.1056/nejm198812223192527
  2. 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
  3. Anichini A., Melanoma cells and normal melanocytes share antigens recognized by HLA- A2-restricted cytotoxic T cell clones from melanoma patients, 10.1084/jem.177.4.989
  4. Quaglino, Ann Oncol
  5. Le Gal Frédérique-Anne, Lefebvre Philippe, Deschemin Jean-Christophe, Andrieu Muriel, Guillet Jean-Gérard, Avril Marie-Françoise, Bosq Jacques, Dore Martin-Xavier, Direct Evidence to Support the Role of Antigen-Specific CD8+ T Cells in Melanoma-Associated Vitiligo, 10.1046/j.0022-202x.2001.01605.x
  6. Zou Weiping, Regulatory T cells, tumour immunity and immunotherapy, 10.1038/nri1806
  7. Filipazzi Paola, Valenti Roberta, Huber Veronica, Pilla Lorenzo, Canese Paola, Iero Manuela, Castelli Chiara, Mariani Luigi, Parmiani Giorgio, Rivoltini Licia, Identification of a New Subset of Myeloid Suppressor Cells in Peripheral Blood of Melanoma Patients With Modulation by a Granulocyte-Macrophage Colony-Stimulation Factor–Based Antitumor Vaccine, 10.1200/jco.2006.08.5829
  8. 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
  9. Freeman Gordon J., Long Andrew J., Iwai Yoshiko, Bourque Karen, Chernova Tatyana, Nishimura Hiroyuki, Fitz Lori J., Malenkovich Nelly, Okazaki Taku, Byrne Michael C., Horton Heidi F., Fouser Lynette, Carter Laura, Ling Vincent, Bowman Michael R., Carreno Beatriz M., Collins Mary, Wood Clive R., Honjo Tasuku, Engagement of the Pd-1 Immunoinhibitory Receptor by a Novel B7 Family Member Leads to Negative Regulation of Lymphocyte Activation, 10.1084/jem.192.7.1027
  10. Blank Christian, Mackensen Andreas, Contribution of the PD-L1/PD-1 pathway to T-cell exhaustion: an update on implications for chronic infections and tumor evasion, 10.1007/s00262-006-0272-1
  11. Schwartzentruber, J Immunol, 146, 3674 (1991)
  12. Sander Birgitta, Boeryd Bernt, Tumor necrosis factor-Α expression in human primary malignant melanoma and its relationship to tumor infiltration by CD3+ cells, 10.1002/(sici)1097-0215(19960328)66:1<42::aid-ijc8>;2-z
  13. Torisu Hitoe, Ono Mayumi, Kiryu Hiromaro, Furue Masutaka, Ohmoto Yasukazu, Nakayama Juichiro, Nishioka Yasuhiko, Sone Saburo, Kuwano Michihiko, Macrophage infiltration correlates with tumor stage and angiogenesis in human malignant melanoma: Possible involvement of TNFα and IL-1α, 10.1002/(sici)1097-0215(20000115)85:2<182::aid-ijc6>;2-m
  14. Boehm U., Klamp T., Groot M., Howard J. C., CELLULAR RESPONSES TO INTERFERON-γ, 10.1146/annurev.immunol.15.1.749
  15. Strehl Britta, Seifert Ulrike, Kruger Elke, Heink Sylvia, Kuckelkorn Ulrike, Kloetzel Peter-M., Interferon-gamma, the functional plasticity of the ubiquitin-proteasome system, and MHC class I antigen processing, 10.1111/j.0105-2896.2005.00308.x
  16. Kholmanskikh Olga, Loriot Axelle, Brasseur Francis, De Plaen Etienne, De Smet Charles, Expression ofBORISin melanoma: Lack of association withMAGE-A1activation, 10.1002/ijc.23140
  17. Penzo Marianna, Massa Paul E., Olivotto Eleonora, Bianchi Francesca, Borzi Rosa Maria, Hanidu Adedayo, Li Xiang, Li Jun, Marcu Kenneth B., Sustained NF-κB activation produces a short-term cell proliferation block in conjunction with repressing effectors of cell cycle progression controlled by E2F or FoxM1, 10.1002/jcp.21596
  18. Davis Leonard G., Dibner Mark D., Battey James F., Guanidine Isothiocyanate Preparation of Total RNA, Basic Methods in Molecular Biology (1986) ISBN:9780444010827 p.130-135, 10.1016/b978-0-444-01082-7.50040-0
  19. 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
  20. Harada, Cancer Res, 61, 1089 (2001)
  21. 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
  22. 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
  23. Certa Ulrich, Seiler Monika, Padovan Elisabetta, Spagnoli Giulio C., Interferon-α Sensitivity in Melanoma Cells: Detection of Potential Response Marker Genes, Cancers of the Skin (2002) ISBN:9783642639692 p.85-91, 10.1007/978-3-642-59410-6_12
  24. Dinarello Charles A., Immunological and Inflammatory Functions of the Interleukin-1 Family, 10.1146/annurev.immunol.021908.132612
  25. Apte Ron N., Voronov Elena, Is interleukin-1 a good or bad ‘guy’ in tumor immunobiology and immunotherapy?, 10.1111/j.1600-065x.2008.00615.x
  26. Du Jinyan, Fisher David E., Identification ofAim-1as theunderwhiteMouse Mutant and Its Transcriptional Regulation by MITF, 10.1074/jbc.m110229200
  27. Du Jinyan, Miller Arlo J., Widlund Hans R., Horstmann Martin A., Ramaswamy Sridhar, Fisher David E., MLANA/MART1 and SILV/PMEL17/GP100 Are Transcriptionally Regulated by MITF in Melanocytes and Melanoma, 10.1016/s0002-9440(10)63657-7
  28. Schadendorf, J Immunol, 151, 2667 (1993)
  29. Singh, Cancer Res, 58, 1532 (1998)
  30. Bennicelli, Cancer Res, 49, 930 (1989)
  31. Elaraj D. M., The Role of Interleukin 1 in Growth and Metastasis of Human Cancer Xenografts, 10.1158/1078-0432.ccr-05-1603
  32. Hiscott J, Marois J, Garoufalis J, D'Addario M, Roulston A, Kwan I, Pepin N, Lacoste J, Nguyen H, Bensi G, Characterization of a functional NF-kappa B site in the human interleukin 1 beta promoter: evidence for a positive autoregulatory loop., 10.1128/mcb.13.10.6231
  33. Niu Jiangong, Li Zhongkui, Peng Bailu, Chiao Paul J., Identification of an Autoregulatory Feedback Pathway Involving Interleukin-1α in Induction of Constitutive NF-κB Activation in Pancreatic Cancer Cells, 10.1074/jbc.m309789200
  34. Kim, Int J Biochem Cell Biol, 36, 1482 (2004)
  35. Gollob Jared A., Sciambi Catherine J., Huang Zhiqing, Dressman Holly K., Gene Expression Changes and Signaling Events Associated with the Direct Antimelanoma Effect of IFN-γ, 10.1158/0008-5472.can-05-1387
  36. Naugler Willscott E, Karin Michael, NF-κB and cancer—identifying targets and mechanisms, 10.1016/j.gde.2008.01.020
  37. Taganov K. D., Boldin M. P., Chang K.-J., Baltimore D., NF- B-dependent induction of microRNA miR-146, an inhibitor targeted to signaling proteins of innate immune responses, 10.1073/pnas.0605298103
  38. 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
  39. Cohen, Clin Cancer Res, 8, 3728 (2002)
  40. Kono M., Dunn I. S., Durda P. J., Butera D., Rose L. B., Haggerty T. J., Benson E. M., Kurnick J. T., Role of the Mitogen-Activated Protein Kinase Signaling Pathway in the Regulation of Human Melanocytic Antigen Expression, 10.1158/1541-7786.mcr-06-0077
  41. Verstrepen L., Bekaert T., Chau T.-L., Tavernier J., Chariot A., Beyaert R., TLR-4, IL-1R and TNF-R signaling to NF-κB: variations on a common theme, 10.1007/s00018-008-8064-8
  42. Morel Sandra, Lévy Frédéric, Burlet-Schiltz Odile, Brasseur Francis, Probst-Kepper Michaël, Peitrequin Anne-Lise, Monsarrat Bernard, Van Velthoven Robert, Cerottini Jean-Charles, Boon Thierry, Gairin Jean Edouard, Van den Eynde Benoît J., Processing of Some Antigens by the Standard Proteasome but Not by the Immunoproteasome Results in Poor Presentation by Dendritic Cells, 10.1016/s1074-7613(00)80163-6
  43. Leblond Jonathan, Hubert-Buron Aurélie, Bole-Feysot Christine, Ducrotté Philippe, Déchelotte Pierre, Coëffier Moïse, Regulation of proteolysis by cytokines in the human intestinal epithelial cell line HCT–8: role of IFNγ, 10.1016/j.biochi.2006.01.003
  44. Nagorsen Dirk, Servis Catherine, L�vy Nicole, Provenzano Maurizio, Dudley MarkE., Marincola FrancescoM., L�vy Fr�d�ric, Proteasomal cleavage does not determine immunogenicity of gp100-derived peptides gp100209-217 and gp100209-217T210M, 10.1007/s00262-004-0532-x
  45. Kurnick J. T., Ramirez-Montagut T., Boyle L. A., Andrews D. M., Pandolfi F., Durda P. J., Butera D., Dunn I. S., Benson E. M., Gobin S. J. P., van den Elsen P. J., A Novel Autocrine Pathway of Tumor Escape from Immune Recognition: Melanoma Cell Lines Produce a Soluble Protein That Diminishes Expression of the Gene Encoding the Melanocyte Lineage Melan-A/MART-1 Antigen Through Down-Modulation of Its Promoter, 10.4049/jimmunol.167.3.1204
  46. Durda, Mol Cancer Res, 1, 411 (2003)
  47. Lewis Anne M, Varghese Sheelu, Xu Hui, Alexander H Richard, 10.1186/1479-5876-4-48
  48. Vachtenheim J., Novotna H., Ghanem G., Transcriptional Repression of the Microphthalmia Gene in Melanoma Cells Correlates with the Unresponsiveness of Target Genes to Ectopic Microphthalmia-Associated Transcription Factor, 10.1046/j.0022-202x.2001.01563.x
  49. Fang D., Selective down-regulation of tyrosinase family gene TYRP1 by inhibition of the activity of melanocyte transcription factor, MITF, 10.1093/nar/gkf424
  50. Li Ling, Dragulev Bojan, Zigrino Paola, Mauch Cornelia, Fox Jay W., The invasive potential of human melanoma cell lines correlates with their ability to alter fibroblast gene expressionin vitroand the stromal microenvironmentin vivo, 10.1002/ijc.24463