Analysis of CTCL cell lines reveals important differences between mycosis fungoides/Sezary syndrome vs. HTLV-1(+) leukemic cell lines

作者：Netchiporouk Elena; Gantchev Jennifer; Tsang Matthew; Thibault Philippe; Watters Andrew K; Hughes John Douglas Matthew; Ghazawi Feras M; Woetmann Anders; Odum Niels; Sasseville Denis^*; Litvinov Ivan V^*

来源：Oncotarget, 2017, 8(56): 95981-95998.

DOI：10.18632/oncotarget.21619

• human T-cell lymphotropic virus type 1
• cutaneous T-cell lymphomas
• spectral karyotyping
• gene expression analysis
• xenograft tumors

HTLV-1 is estimated to affect similar to 20 million people worldwide and in similar to 5% of carriers it produces Adult T-Cell Leukemia/Lymphoma (ATLL), which can often masquerade and present with classic erythematous pruritic patches and plaques that are typically seen in Mycosis Fungoides (MF) and Sezary Syndrome (SS), the most recognized variants of Cutaneous T-Cell Lymphomas (CTCL). For many years the role of HTLV1 in the pathogenesis of MF/SS has been hotly debated. In this study we analyzed CTCL vs. HTLV-1(+) leukemic cells. We performed G-banding/spectral karyotyping, extensive gene expression analysis, TP53 sequencing in the 11 patient-derived HTLV1(+) (MJ and Hut102) vs. HTLV-1-(Myla, Mac2a, PB2B, HH, H9, Hut78, SZ4, Sez4 and SeAx) CTCL cell lines. We further tested drug sensitivities to commonly used CTCL therapies and studied the ability of these cells to produce subcutaneous xenograft tumors in NOD. Cg-Prkdc(scid) Il2rg(tm1Wjl)/SzJ mice. Our work demonstrates that unlike classic advanced MF/SS cells that acquire many ongoing balanced and unbalanced chromosomal translocations, HTLV-1(+) CTCL leukemia cells are diploid and exhibit only a minimal number of non-specific chromosomal alterations. Our results indicate that HTLV-1 virus is likely not involved in the pathogenesis of classic MF/SS since it drives a very different pathway of lymphomagenesis based on our findings in these cells. This study also provides for the first time a comprehensive characterization of the CTCL cells with respect to gene expression profiling, TP53 mutation status, ability to produce tumors in mice and response to commonly used therapies.

• 出版日期2017-11-10
• 单位McGill