The Peripheral T-Cell Lymphomas. Группа авторов

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The Peripheral T-Cell Lymphomas - Группа авторов

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      Molecular analysis has shed light on the diversity and hierarchy of genetic events linked to T

      LdL is supported by a grant of the Swiss National Foundation.

       Heavican, T.B., Bouska, A., Yu,. J, et al. (2019). Genetic drivers of oncogenic pathways in molecular subgroups of peripheral T‐cell lymphoma. Blood 133(15):1664–1676.

       Lemonnier, F., Couronné, L., Parrens, M., et al. (2012). Recurrent TET2 mutations in peripheral T‐cell lymphomas correlate with TFH‐like features and adverse clinical parameters. Blood 120(7):1466–1469.

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      3 3 Abate, F., da Silva‐Almeida, A.C., Zairs, S. et al. (2017). Activating mutations and translocations in the guanine exchange factor VAV1 in peripheral T‐cell lymphomas. Proc Natl Acad Sci U S A 114 (4): 764–769.

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      5 5 Vallois, D., Dupuy, A., Lemonnier, F. et al. (2018). RNA fusions involving CD28 are rare in peripheral T‐cell lymphomas and concentrate mainly in those derived from follicular helper T cells. Haematologica 103 (8): e360–e363.

      6 6 Heavican, T.B., Bouska, A., Yu, J. et al. (2019). Genetic drivers of oncogenic pathways in molecular subgroups of peripheral T‐cell lymphoma. Blood 133 (15): 1664–1676.

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      9 9 Kataoka, K., Shiraishi, Y., Takeda, Y. et al. (2016). Aberrant PD‐L1 expression through 3’‐UTR disruption in multiple cancers. Nature 534 (7607): 402–406.

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      12 12 Valleron, W., Ysebaert, L., Berquet, L. et al. (2012). Small nucleolar RNA expression profiling identifies potential prognostic markers in peripheral T‐cell lymphoma. Blood 120 (19): 3997–4005.

      13 13 Wang, L., Ni, X., Covington, K.R. et al. (2015). Genomic profiling of Sezary syndrome identifies alterations of key T cell signaling and differentiation genes. Nat Genet 47 (12): 1426–1434.

      14 14 Sakata‐Yanagimoto, M., Enami, T., Yoshida, K. et al. (2014). Somatic RHOA mutation in angioimmunoblastic T cell lymphoma. Nat Genet 46 (2): 171–175.

      15 15 Odejide, O., Weigert, O., Lane, A.A. et al. (2014). A targeted mutational landscape of angioimmunoblastic T‐cell lymphoma. Blood 123 (9): 1293–1296.

      16 16 Lemonnier, F., Couronné, L., Parrens, M. et al. (2012). Recurrent TET2 mutations in peripheral T‐cell lymphomas correlate with TFH‐like features and adverse clinical parameters. Blood 120 (7): 1466–1469.

      17 17 Couronné, L., Bastard, C., and Bernard, O.A. (2012). TET2 and DNMT3A mutations in human T‐cell lymphoma. N Engl J Med 366 (1): 95–96.

      18 18 Cairns, R.A., Iqbal, J., Lemonnier, F. et al. (2012). IDH2 mutations are frequent in angioimmunoblastic T‐cell lymphoma. Blood 119 (8): 1901–1903.

      19 19 Solary, E., Bernard, O.A., Tefferi, A. et al. (2014). The Ten‐Eleven Translocation‐2 (TET2) gene in hematopoiesis and hematopoietic diseases. Leukemia 28 (3): 485–496.

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      22 22 Lemonnier, F., Poullot, E., Dupuy, A. et al. (2018). Loss of 5‐hydroxymethylcytosine is a frequent event in peripheral T‐cell lymphomas. Haematologica 103 (3): e115–e118.

      23 23 Roberti, A., Dobay, M.P., Bisig, B. et al. (2016). Type II enteropathy‐associated T‐cell lymphoma features a unique genomic profile with highly recurrent SETD2 alterations. Nat Commun 7: 12602.

      24 24 McKinney, M., Moffitt, A.B., Gaulard, P. et al. (2017). The genetic basis of hepatosplenic T‐cell lymphoma. Cancer Discov 7 (4): 369–379.

      25 25 Jiang, L., Gu, Z.H., Yan, Z.X. et al. (2015). Exome sequencing identifies somatic mutations of DDX3X in natural killer/T‐cell lymphoma. Nat Genet 47 (9): 1061–1066.

      26 26 Li, Z., Zhang, X., Xue, W. et al. (2019). Recurrent GNAQ mutation encoding T96S in natural killer/T cell lymphoma. Nat Commun 10 (1): 4209–4209.

      27 27 Ji, M.M., Huang, Y.H., Huang, J.Y. et al. (2018). Histone modifier gene mutations in peripheral T‐cell lymphoma not otherwise specified. Haematologica 103 (4): 679–687.

      28 28 Laurent, C., Nicolae, A., Laurent, C. et al. (2020). Gene alterations in epigenetic modifiers and JAK‐STAT signaling are frequent in breast implant–associated ALCL. Blood 135 (5): 360–370.

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      30 30 Jaiswal, S., Fontanillas, P., Flannick, J. et al. (2014). Age‐related clonal hematopoiesis associated with adverse outcomes. N Engl J Med 371 (26): 2488–2498.

      31 31 Quivoron, C., Couronné, L., Della Valle, V. et al. (2011). TET2 inactivation results in pleiotropic hematopoietic abnormalities in mouse and is a recurrent event during human

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