| Literature DB >> 30792187 |
Chantana Polprasert1,2, Yasuhide Takeuchi3,4, Nobuyuki Kakiuchi3, Kenichi Yoshida3, Thamathorn Assanasen5, Wimonmas Sitthi5, Udomsak Bunworasate1,2, Arunrat Pirunsarn6, Kitsada Wudhikarn1,2, Panisinee Lawasut1,2, Noppacharn Uaprasert1, Sunisa Kongkiatkamon1,2, Chatphatai Moonla1, Masashi Sanada7, Nobuhiro Akita8, June Takeda3, Yoichi Fujii3, Hiromichi Suzuki3, Yasuhito Nannya3, Yuichi Shiraishi9, Kenichi Chiba9, Hiroko Tanaka9, Satoru Miyano9, Ponlapat Rojnuckarin1,2, Seishi Ogawa3, Hideki Makishima3.
Abstract
Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare subtype of peripheral T-cell lymphoma affecting younger patients and associated with hemophagocytic lymphohistiocytosis. To clarify the molecular pathogenesis of SPTCL, we analyzed paired tumor and germline DNAs from 13 patients by whole-exome sequencing. All cases were Asians and were phenotypically sporadic with no family history of SPTCL. Consistent with a recent report, germline mutations in HAVCR2, encoding T-cell immunoglobulin mucin 3 (TIM3), were identified in 11 of 13 (85%) cases. All mutated cases were primary SPTCL, whereas the 2 cases without mutation were secondary SPTCL associated with underlying diseases, including viral infection and autoimmune disease. Ten patients harbored homozygous p.Y82C mutations, and 1 showed compound heterozygous mutations (p.Y82C and p.T101I). Both missense mutations altered highly conserved residues located in the extracellular immunoglobulin variable-like domain. According to the Genome Aggregation Database of >138 500 general individuals, both mutations were documented with minor allele frequencies < 0.007, indicating remarkable enrichment of these HAVCR2 alleles in SPTCL. SPTCL cells also harbored somatic mutations (6.2 per patient) that are frequently identified in genes associated with epigenetic regulation and signal transduction. In conclusion, individuals harboring biallelic HAVCR2 (TIM3) germline mutations were highly susceptible to sporadic SPTCL, which was also associated with clonal somatic mutations.Entities:
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Year: 2019 PMID: 30792187 PMCID: PMC6391671 DOI: 10.1182/bloodadvances.2018028340
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529