The Eph-Receptor A7 Is a Soluble Tumor Suppressor for Follicular Lymphoma
Tài liệu tham khảo
Barr, 2008, Follicular non-Hodgkin lymphoma: long-term results of stem-cell transplantation, Curr. Opin. Oncol., 20, 502, 10.1097/CCO.0b013e32830b61ac
Bende, 2007, Molecular pathways in follicular lymphoma, Leukemia, 21, 18, 10.1038/sj.leu.2404426
Bidere, 2009, Casein kinase 1alpha governs antigen-receptor-induced NF-kappaB activation and human lymphoma cell survival, Nature, 458, 92, 10.1038/nature07613
Calado, 2010, Constitutive canonical NF-kappaB activation cooperates with disruption of BLIMP1 in the pathogenesis of activated B cell-like diffuse large cell lymphoma, Cancer Cell, 18, 580, 10.1016/j.ccr.2010.11.024
Chin, 2008, Translating insights from the cancer genome into clinical practice, Nature, 452, 553, 10.1038/nature06914
Compagno, 2009, Mutations of multiple genes cause deregulation of NF-kappaB in diffuse large B-cell lymphoma, Nature, 459, 717, 10.1038/nature07968
Dawson, 2007, Global DNA methylation profiling reveals silencing of a secreted form of Epha7 in mouse and human germinal center B-cell lymphomas, Oncogene, 26, 4243, 10.1038/sj.onc.1210211
Dickins, 2005, Probing tumor phenotypes using stable and regulated synthetic microRNA precursors, Nat. Genet., 37, 1289, 10.1038/ng1651
Ding, 2008, Somatic mutations affect key pathways in lung adenocarcinoma, Nature, 455, 1069, 10.1038/nature07423
Egle, 2004, VavP-Bcl2 transgenic mice develop follicular lymphoma preceded by germinal center hyperplasia, Blood, 103, 2276, 10.1182/blood-2003-07-2469
Feldser, 2010, Stage-specific sensitivity to p53 restoration during lung cancer progression, Nature, 468, 572, 10.1038/nature09535
Gaidano, 1992, Deletions involving two distinct regions of 6q in B-cell non-Hodgkin lymphoma, Blood, 80, 1781, 10.1182/blood.V80.7.1781.1781
Hauptschein, 1998, Cloning and mapping of human chromosome 6q26-q27 deleted in B-cell non-Hodgkin lymphoma and multiple tumor types, Genomics, 50, 170, 10.1006/geno.1998.5321
Heyer, 2010, Non-germline genetically engineered mouse models for translational cancer research, Nat. Rev. Cancer, 10, 470, 10.1038/nrc2877
Himanen, 2010, Architecture of Eph receptor clusters, Proc. Natl. Acad. Sci. USA, 107, 10860, 10.1073/pnas.1004148107
Holmberg, 2000, Regulation of repulsion versus adhesion by different splice forms of an Eph receptor, Nature, 408, 203, 10.1038/35041577
Johnson, 2009, Lymphomas with concurrent BCL2 and MYC translocations: the critical factors associated with survival, Blood, 114, 2273, 10.1182/blood-2009-03-212191
Kato, 2009, Frequent inactivation of A20 in B-cell lymphomas, Nature, 459, 712, 10.1038/nature07969
Klein, 2008, Germinal centres: role in B-cell physiology and malignancy, Nat. Rev. Immunol., 8, 22, 10.1038/nri2217
Kuang, 2010, Aberrant DNA methylation and epigenetic inactivation of Eph receptor tyrosine kinases and ephrin ligands in acute lymphoblastic leukemia, Blood, 115, 2412, 10.1182/blood-2009-05-222208
Lenz, 2008, Oncogenic CARD11 mutations in human diffuse large B cell lymphoma, Science, 319, 1676, 10.1126/science.1153629
Macrae, 2005, A conditional feedback loop regulates Ras activity through EphA2, Cancer Cell, 8, 111, 10.1016/j.ccr.2005.07.005
Maloney, 2003, Rituximab for follicular lymphoma, Curr. Hematol. Rep., 2, 13
Mandelbaum, 2010, BLIMP1 is a tumor suppressor gene frequently disrupted in activated B cell-like diffuse large B cell lymphoma, Cancer Cell, 18, 568, 10.1016/j.ccr.2010.10.030
Mavrakis, 2010, Genome-wide RNA-mediated interference screen identifies miR-19 targets in Notch-induced T-cell acute lymphoblastic leukaemia, Nat. Cell Biol., 12, 372, 10.1038/ncb2037
McBride, 2008, Regulation of class switch recombination and somatic mutation by AID phosphorylation, J. Exp. Med., 205, 2585, 10.1084/jem.20081319
McCaffrey, 2002, RNA interference in adult mice, Nature, 418, 38, 10.1038/418038a
Nanjangud, 2007, Molecular cytogenetic analysis of follicular lymphoma (FL) provides detailed characterization of chromosomal instability associated with the t(14;18)(q32;q21) positive and negative subsets and histologic progression, Cytogenet. Genome Res., 118, 337, 10.1159/000108318
Ngo, 2011, Oncogenically active MYD88 mutations in human lymphoma, Nature, 470, 115, 10.1038/nature09671
Noren, 2006, The EphB4 receptor suppresses breast cancer cell tumorigenicity through an Abl-Crk pathway, Nat. Cell Biol., 8, 815, 10.1038/ncb1438
Novak, 2009, The NF-{kappa}B negative regulator TNFAIP3 (A20) is inactivated by somatic mutations and genomic deletions in marginal zone lymphomas, Blood, 113, 4918, 10.1182/blood-2008-08-174110
Offit, 1993, 6q deletions define distinct clinico-pathologic subsets of non-Hodgkin's lymphoma, Blood, 82, 2157, 10.1182/blood.V82.7.2157.2157
Oricchio, 2010, Mouse models of cancer as biological filters for complex genomic data, Dis. Model Mech., 11-12, 701, 10.1242/dmm.006296
Pasquale, 2008, Eph-ephrin bidirectional signaling in physiology and disease, Cell, 133, 38, 10.1016/j.cell.2008.03.011
Pasquale, 2010, Eph receptors and ephrins in cancer: bidirectional signalling and beyond, Nat. Rev. Cancer, 10, 165, 10.1038/nrc2806
Pasqualucci, 2006, Inactivation of the PRDM1/BLIMP1 gene in diffuse large B cell lymphoma, J. Exp. Med., 203, 311, 10.1084/jem.20052204
Relander, 2010, Prognostic factors in follicular lymphoma, J. Clin. Oncol., 28, 2902, 10.1200/JCO.2009.26.1693
Schmitz, 2009, TNFAIP3 (A20) is a tumor suppressor gene in Hodgkin lymphoma and primary mediastinal B cell lymphoma, J. Exp. Med., 206, 981, 10.1084/jem.20090528
Seiradake, 2010, An extracellular steric seeding mechanism for Eph-ephrin signaling platform assembly, Nat. Struct. Mol. Biol., 17, 398, 10.1038/nsmb.1782
Shaffer, 2008, IRF4 addiction in multiple myeloma, Nature, 454, 226, 10.1038/nature07064
Smith, 2004, Dissecting the EphA3/Ephrin-A5 interactions using a novel functional mutagenesis screen, J. Biol. Chem., 279, 9522, 10.1074/jbc.M309326200
Valenzuela, 1995, Identification of full-length and truncated forms of Ehk-3, a novel member of the Eph receptor tyrosine kinase family, Oncogene, 10, 1573
Velculescu, 2008, Defining the blueprint of the cancer genome, Carcinogenesis, 29, 1087, 10.1093/carcin/bgn096
Ventura, 2007, Restoration of p53 function leads to tumour regression in vivo, Nature, 445, 661, 10.1038/nature05541
Viardot, 2002, Clinicopathologic correlations of genomic gains and losses in follicular lymphoma, J. Clin. Oncol., 20, 4523, 10.1200/JCO.2002.12.006
Wendel, 2004, Survival signalling by Akt and eIF4E in oncogenesis and cancer therapy, Nature, 428, 332, 10.1038/nature02369
Xue, 2007, Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas, Nature, 445, 656, 10.1038/nature05529
Zender, 2008, An oncogenomics-based in vivo RNAi screen identifies tumor suppressors in liver cancer, Cell, 135, 852, 10.1016/j.cell.2008.09.061
Antipenko, A., Himanen, J.P., van Leyen, K., Nardi-Dei, V., Lesniak, J., Barton, W.A., Rajashankar, K.R., Lu, M., Hoemme, C., Puschel, A.W., et al. (2003). Structure of the semaphorin-3A receptor binding module. Neuron 39, 589–598.
Bergers, G., Javaherian, K., Lo, K.M., Folkman, J., and Hanahan, D. (1999). Effects of angiogenesis inhibitors on multistage carcinogenesis in mice. Science 284, 808–812.
Chen, K., McLellan, M.D., Ding, L., Wendl, M.C., Kasai, Y., Wilson, R.K., and Mardis, E.R. (2007). PolyScan: an automatic indel and SNP detection approach to the analysis of human resequencing data. Genome Res. 17, 659–666.
Dickins, R.A., Hemann, M.T., Zilfou, J.T., Simpson, D.R., Ibarra, I., Hannon, G.J., and Lowe, S.W. (2005). Probing tumor phenotypes using stable and regulated synthetic microRNA precursors. Nat. Genet. 37, 1289–1295.
Egle, A., Harris, A.W., Bath, M.L., O'Reilly, L., and Cory, S. (2004). VavP-Bcl2 transgenic mice develop follicular lymphoma preceded by germinal center hyperplasia. Blood 103, 2276–2283.
Gordon, D., Abajian, C., and Green, P. (1998). Consed: a graphical tool for sequence finishing. Genome Res. 8, 195–202.
Himanen, J.P., Henkemeyer, M., and Nikolov, D.B. (1998). Crystal structure of the ligand-binding domain of the receptor tyrosine kinase EphB2. Nature 396, 486–491.
Mandelbaum, J., Bhagat, G., Tang, H., Mo, T., Brahmachary, M., Shen, Q., Chadburn, A., Rajewsky, K., Tarakhovsky, A., Pasqualucci, L., et al. (2010). BLIMP1 Is a Tumor Suppressor Gene Frequently Disrupted in Activated B Cell-like Diffuse Large B Cell Lymphoma. Cancer Cell 18, 568–579.
Mavrakis, K.J., Wolfe, A.L., Oricchio, E., Palomero, T., de Keersmaecker, K., McJunkin, K., Zuber, J., James, T., Khan, A.A., Leslie, C.S., et al. (2010). Genome-wide RNA-mediated interference screen identifies miR-19 targets in Notch-induced T cell acute lymphoblastic leukemia. Nat. Cell Biol. 12, 372–379.
Mavrakis, K.J., Zhu, H., Silva, R.L., Mills, J.R., Teruya-Feldstein, J., Lowe, S.W., Tam, W., Pelletier, J., and Wendel, H.G. (2008). Tumorigenic activity and therapeutic inhibition of Rheb GTPase. Genes Dev. 22, 2178–2188.
McBride, K.M., Gazumyan, A., Woo, E.M., Schwickert, T.A., Chait, B.T., and Nussenzweig, M.C. (2008). Regulation of class switch recombination and somatic mutation by AID phosphorylation. J. Exp. Med. 205, 2585–2594.
Nickerson, D.A., Tobe, V.O., and Taylor, S.L. (1997). PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing. Nucleic Acids Res. 25, 2745–2751.
Scott, C.L., Gil, J., Hernando, E., Teruya-Feldstein, J., Narita, M., Martinez, D., Visakorpi, T., Mu, D., Cordon-Cardo, C., Peters, G., et al. (2007). Role of the chromobox protein CBX7 in lymphomagenesis. Proc. Natl. Acad. Sci. USA 104, 5389–5394.
Shaknovich, R., Figueroa, M.E., and Melnick, A. (2010). HELP (HpaII tiny fragment enrichment by ligation-mediated PCR) assay for DNA methylation profiling of primary normal and malignant B lymphocytes. Methods Mol. Biol. 632, 191–201.
Thompson, R.F., Reimers, M., Khulan, B., Gissot, M., Richmond, T.A., Chen, Q., Zheng, X., Kim, K., and Greally, J.M. (2008). An analytical pipeline for genomic representations used for cytosine methylation studies. Bioinformatics 24, 1161–1167.
Veeriah, S., Taylor, B.S., Meng, S., Fang, F., Yilmaz, E., Vivanco, I., Janakiraman, M., Schultz, N., Hanrahan, A.J., Pao, W., et al. (2010). Somatic mutations of the Parkinson's disease-associated gene PARK2 in glioblastoma and other human malignancies. Nat. Genet. 42, 77–82.
Wendel, H.G., de Stanchina, E., Cepero, E., Ray, S., Emig, M., Fridman, J.S., Veach, D.R., Bornmann, W.G., Clarkson, B., McCombie, W.R., et al. (2006). Loss of p53 impedes the antileukemic response to BCR-ABL inhibition. Proc. Natl. Acad. Sci. USA 103, 7444–7449.
Wendel, H.G., De Stanchina, E., Fridman, J.S., Malina, A., Ray, S., Kogan, S., Cordon-Cardo, C., Pelletier, J., and Lowe, S.W. (2004). Survival signaling by Akt and eIF4E in oncogenesis and cancer therapy. Nature 428, 332–337.
Xu, K., Rajashankar, K.R., Chan, Y.P., Himanen, J.P., Broder, C.C., and Nikolov, D.B. (2008). Host cell recognition by the henipaviruses: crystal structures of the Nipah G attachment glycoprotein and its complex with ephrin-B3. Proc. Natl. Acad. Sci. USA 105, 9953–9958.
Yu, D., and Thomas-Tikhonenko, A. (2002). A non-transgenic mouse model for B cell lymphoma: in vivo infection of p53-null bone marrow progenitors by a Myc retrovirus is sufficient for tumorigenesis. Oncogene 21, 1922–1927.