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==References==
==References==
Barbaux, S., Niaudet, P., Gubler, M.C., Grünfeld, J.P., Jaubert, F., Kuttenn, F., Fékété, C.N., Souleyreau-Therville, N., Thibaud, E., Fellous, M., et al. (1997). Donor splice-site mutations in WT1 are responsible for Frasier syndrome. Nat. Genet. 17, 467–470. PMID: 9398852
Brayer, J., Lancet, J.E., Powers, J., List, A., Balducci, L., Komrokji, R., and Pinilla-Ibarz, J. (2015). WT1 vaccination in AML and MDS: A pilot trial with synthetic analog peptides. Am J Hematol 90, 602–607. PMID: 25802083
Breslow, N.E., Beckwith, J.B., Perlman, E.J., and Reeve, A.E. (2006). Age distributions, birth weights, nephrogenic rests, and heterogeneity in the pathogenesis of Wilms tumor. Pediatric Blood & Cancer 47, 260–267. PMID: 16700047
Call, K.M., Glaser, T., Ito, C.Y., Buckler, A.J., Pelletier, J., Haber, D.A., Rose, E.A., Kral, A., Yeger, H., and Lewis, W.H. (1990). Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms’ tumor locus. Cell 60, 509–520. PMID: 2154335
Di Stasi, A., Jimenez, A.M., Minagawa, K., Al-Obaidi, M., and Rezvani, K. (2015). Review of the Results of WT1 Peptide Vaccination Strategies for Myelodysplastic Syndromes and Acute Myeloid Leukemia from Nine Different Studies. Front Immunol 6. PMID: 25699052
Dohi, S., Ohno, S., Ohno, Y., Soma, G.-I., Kyo, S., and Inoue, M. (2009). Correlation between WT1 expression and cell proliferation in endometrial cancer. Anticancer Res. 29, 4887–4891. PMID: 20032452
Gaidzik, V.I., Schlenk, R.F., Moschny, S., Becker, A., Bullinger, L., Corbacioglu, A., Krauter, J., Schlegelberger, B., Ganser, A., Döhner, H., et al. (2009). Prognostic impact of WT1 mutations in cytogenetically normal acute myeloid leukemia: a study of the German-Austrian AML Study Group. Blood 113, 4505–4511. PMID: 19221039
Gessler, M., König, A., Arden, K., Grundy, P., Orkin, S., Sallan, S., Peters, C., Ruyle, S., Mandell, J., and Li, F. (1994). Infrequent mutation of the WT1 gene in 77 Wilms’ Tumors. Hum. Mutat. 3, 212–222. PMID: 8019557
Haber, D.A., Sohn, R.L., Buckler, A.J., Pelletier, J., Call, K.M., and Housman, D.E. (1991). Alternative splicing and genomic structure of the Wilms tumor gene WT1. Proc. Natl. Acad. Sci. U.S.A. 88, 9618–9622. PMID: 1658787
Hammes, A., Guo, J.K., Lutsch, G., Leheste, J.R., Landrock, D., Ziegler, U., Gubler, M.C., and Schedl, A. (2001). Two splice variants of the Wilms’ tumor 1 gene have distinct functions during sex determination and nephron formation. Cell 106, 319–329. PMID: 11509181
Hastie, N.D. (2017). Wilms’ tumour 1 (WT1) in development, homeostasis and disease. Development 144, 2862–2872. PMID: 28811308
Hewitt, S.M., Hamada, S., McDonnell, T.J., Rauscher, F.J., and Saunders, G.F. (1995). Regulation of the Proto-oncogenes bcl-2 and c-myc by the Wilms’ Tumor Suppressor Gene WT1. Cancer Res 55, 5386–5389. PMID: 7585606
Hollink, I.H.I.M., van den Heuvel-Eibrink, M.M., Zimmermann, M., Balgobind, B.V., Arentsen-Peters, S.T.C.J.M., Alders, M., Willasch, A., Kaspers, G.J.L., Trka, J., Baruchel, A., et al. (2009). Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia. Blood 113, 5951–5960. PMID: 19171881
Huff, V., and Saunders, G.F. (1993). Wilms tumor genes. Biochim. Biophys. Acta 1155, 295–306.
Hylander, B., Repasky, E., Shrikant, P., Intengan, M., Beck, A., Driscoll, D., Singhal, P., Lele, S., and Odunsi, K. (2006). Expression of Wilms tumor gene (WT1) in epithelial ovarian cancer. Gynecol. Oncol. 101, 12–17. PMID: 16263157
Köbel, M., Kalloger, S.E., Boyd, N., McKinney, S., Mehl, E., Palmer, C., Leung, S., Bowen, N.J., Ionescu, D.N., Rajput, A., et al. (2008). Ovarian carcinoma subtypes are different diseases: implications for biomarker studies. PLoS Med. 5, e232. PMID: 19053170
Koido, S., Homma, S., Okamoto, M., Takakura, K., Mori, M., Yoshizaki, S., Tsukinaga, S., Odahara, S., Koyama, S., Imazu, H., et al. (2014). Treatment with chemotherapy and dendritic cells pulsed with multiple Wilms’ tumor 1 (WT1)-specific MHC class I/II-restricted epitopes for pancreatic cancer. Clin. Cancer Res. 20, 4228–4239. PMID: 25056373
Krauth, M.-T., Alpermann, T., Bacher, U., Eder, C., Dicker, F., Ulke, M., Kuznia, S., Nadarajah, N., Kern, W., Haferlach, C., et al. (2015). WT1 mutations are secondary events in AML, show varying frequencies and impact on prognosis between genetic subgroups. Leukemia 29, 660–667. PMID: 25110071
Liu, Z., Yamanouchi, K., Ohtao, T., Matsumura, S., Seino, M., Shridhar, V., Takahashi, T., Takahashi, K., and Kurachi, H. (2014). High Levels of Wilms’ Tumor 1 (WT1) Expression Were Associated with Aggressive Clinical Features in Ovarian Cancer. Anticancer Res 34, 2331–2340. PMID: 24778040
Maheswaran, S., Park, S., Bernard, A., Morris, J.F., Rauscher, F.J., Hill, D.E., and Haber, D.A. (1993). Physical and functional interaction between WT1 and p53 proteins. Proc. Natl. Acad. Sci. U.S.A. 90, 5100–5104. PMID: 8389468
Maiti, S., Alam, R., Amos, C.I., and Huff, V. (2000). Frequent Association of β-Catenin and WT1 Mutations in Wilms Tumors. Cancer Res 60, 6288–6292. PMID: 11103785
Menke, A.L., van der Eb, A.J., and Jochemsen, A.G. (1998). The Wilms’ tumor 1 gene: oncogene or tumor suppressor gene? Int. Rev. Cytol. 181, 151–212. PMID: 9522457
Mikami, T., Hada, T., Chosa, N., Ishisaki, A., Mizuki, H., and Takeda, Y. (2013). Expression of Wilms’ tumor 1 (WT1) in oral squamous cell carcinoma. J. Oral Pathol. Med. 42, 133–139. PMID: 22672247
Netinatsunthorn, W., Hanprasertpong, J., Dechsukhum, C., Leetanaporn, R., and Geater, A. (2006). WT1 gene expression as a prognostic marker in advanced serous epithelial ovarian carcinoma: an immunohistochemical study. BMC Cancer 6, 90. PMID: 16606472
Paschka, P., Marcucci, G., Ruppert, A.S., Whitman, S.P., Mrózek, K., Maharry, K., Langer, C., Baldus, C.D., Zhao, W., Powell, B.L., et al. (2008). Wilms’ tumor 1 gene mutations independently predict poor outcome in adults with cytogenetically normal acute myeloid leukemia: a cancer and leukemia group B study. J. Clin. Oncol. 26, 4595–4602. PMID: 18559874
Pelletier, J., Bruening, W., Kashtan, C.E., Mauer, S.M., Manivel, J.C., Striegel, J.E., Houghton, D.C., Junien, C., Habib, R., and Fouser, L. (1991). Germline mutations in the Wilms’ tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell 67, 437–447. PMID: 1655284
Qi, X., Zhang, F., Wu, H., Liu, J., Zong, B., Xu, C., and Jiang, J. (2015). Wilms’ tumor 1 (WT1) expression and prognosis in solid cancer patients: a systematic review and meta-analysis. Sci Rep 5. PMID: 25748047
Rampal, R., Alkalin, A., Madzo, J., Vasanthakumar, A., Pronier, E., Patel, J., Li, Y., Ahn, J., Abdel-Wahab, O., Shih, A., et al. (2014). DNA Hydroxymethylation Profiling Reveals that WT1 Mutations Result in Loss of TET2 Function in Acute Myeloid Leukemia. Cell Reports 9, 1841–1855. PMID: 25482556
Rauscher, J., Beschorner, R., Gierke, M., Bisdas, S., Braun, C., Ebner, F.H., and Schittenhelm, J. (2014). WT1 expression increases with malignancy and indicates unfavourable outcome in astrocytoma. J. Clin. Pathol. 67, 556–561. PMID: 24607494
Riccardi, V.M., Sujansky, E., Smith, A.C., and Francke, U. (1978). Chromosomal Imbalance in the Aniridia-Wilms’ Tumor Association: 11p Interstitial Deletion. Pediatrics 61, 604–610. PMID: 208044
Richard, D.J., Schumacher, V., Royer-Pokora, B., and Roberts, S.G.E. (2001). Par4 is a coactivator for a splice isoform–specific transcriptional activation domain in WT1. Genes Dev. 15, 328–339. PMID: 11159913
Rivera, M.N., Kim, W.J., Wells, J., Driscoll, D.R., Brannigan, B.W., Han, M., Kim, J.C., Feinberg, A.P., Gerald, W.L., Vargas, S.O., et al. (2007). An X chromosome gene, WTX, is commonly inactivated in Wilms tumor. Science 315, 642–645. PMID: 17204608
Sano, H., Shimada, A., Tabuchi, K., Taki, T., Murata, C., Park, M., Ohki, K., Sotomatsu, M., Adachi, S., Tawa, A., et al. (2013). WT1 mutation in pediatric patients with acute myeloid leukemia: a report from the Japanese Childhood AML Cooperative Study Group. Int. J. Hematol. 98, 437–445. PMID: 23979985
Sawada, A., Inoue, M., Kondo, O., Yamada‐Nakata, K., Ishihara, T., Kuwae, Y., Nishikawa, M., Ammori, Y., Tsuboi, A., Oji, Y., et al. (2016). Feasibility of Cancer Immunotherapy with WT1 Peptide Vaccination for Solid and Hematological Malignancies in Children. Pediatric Blood & Cancer 63, 234–241. PMID: 26469989
Shirakata, T., Oka, Y., Nishida, S., Hosen, N., Tsuboi, A., Oji, Y., Murao, A., Tanaka, H., Nakatsuka, S.-I., Inohara, H., et al. (2012). WT1 peptide therapy for a patient with chemotherapy-resistant salivary gland cancer. Anticancer Res. 32, 1081–1085. PMID: 22399636
Summers, K., Stevens, J., Kakkas, I., Smith, M., Smith, L.L., MacDougall, F., Cavenagh, J., Bonnet, D., Young, B.D., Lister, T.A., et al. (2007). Wilms’ tumour 1 mutations are associated with FLT3-ITD and failure of standard induction chemotherapy in patients with normal karyotype AML. Leukemia 21, 550–551. PMID: 17205055
Suri, M., Kelehan, P., O’Neill, D., Vadeyar, S., Grant, J., Ahmed, S.F., Tolmie, J., McCann, E., Lam, W., Smith, S., et al. (2007). WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations. American Journal of Medical Genetics Part A 143A, 2312–2320. PMID: 17853480
Ujj, Z., Buglyó, G., Udvardy, M., Beyer, D., Vargha, G., Biró, S., and Rejtő, L. (2016). WT1 Expression in Adult Acute Myeloid Leukemia: Assessing its Presence, Magnitude and Temporal Changes as Prognostic Factors. Pathol. Oncol. Res. 22, 217–221. PMID: 26531831
Virappane, P., Gale, R., Hills, R., Kakkas, I., Summers, K., Stevens, J., Allen, C., Green, C., Quentmeier, H., Drexler, H., et al. (2008). Mutation of the Wilms’ tumor 1 gene is a poor prognostic factor associated with chemotherapy resistance in normal karyotype acute myeloid leukemia: the United Kingdom Medical Research Council Adult Leukaemia Working Party. J. Clin. Oncol. 26, 5429–5435. PMID: 18591546
Yang, L., Han, Y., Saiz, F.S., and Minden, M.D. (2007). A tumor suppressor and oncogene: the WT1 story. Leukemia 21, 868–876. PMID: 17361230
== Notes ==
== Notes ==