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北美 ATLL 具有独特的突变和转录特征,并对表观遗传治疗有反应。

North American ATLL has a distinct mutational and transcriptional profile and responds to epigenetic therapies.

机构信息

Department of Oncology, Montefiore Medical Center, Bronx, NY.

Department of Cell Biology and.

出版信息

Blood. 2018 Oct 4;132(14):1507-1518. doi: 10.1182/blood-2018-01-824607. Epub 2018 Aug 13.

Abstract

Adult T-cell leukemia lymphoma (ATLL) is a rare T cell neoplasm that is endemic in Japanese, Caribbean, and Latin American populations. Most North American ATLL patients are of Caribbean descent and are characterized by high rates of chemo-refractory disease and worse prognosis compared with Japanese ATLL. To determine genomic differences between these 2 cohorts, we performed targeted exon sequencing on 30 North American ATLL patients and compared the results with the Japanese ATLL cases. Although the frequency of TP53 mutations was comparable, the mutation frequency in epigenetic and histone modifying genes (57%) was significantly higher, whereas the mutation frequency in JAK/STAT and T-cell receptor/NF-κB pathway genes was significantly lower. The most common type of epigenetic mutation is that affecting EP300 (20%). As a category, epigenetic mutations were associated with adverse prognosis. Dissimilarities with the Japanese cases were also revealed by RNA sequencing analysis of 9 primary patient samples. ATLL samples with a mutated EP300 gene have decreased total and acetyl p53 protein and a transcriptional signature reminiscent of p53-mutated cancers. Most importantly, decitabine has highly selective single-agent activity in the EP300-mutated ATLL samples, suggesting that decitabine treatment induces a synthetic lethal phenotype in EP300-mutated ATLL cells. In conclusion, we demonstrate that North American ATLL has a distinct genomic landscape that is characterized by frequent epigenetic mutations that are targetable preclinically with DNA methyltransferase inhibitors.

摘要

成人 T 细胞白血病淋巴瘤(ATLL)是一种罕见的 T 细胞肿瘤,在日本、加勒比和拉丁美洲人群中流行。大多数北美 ATLL 患者是加勒比裔,与日本 ATLL 患者相比,他们的化疗耐药疾病发生率更高,预后更差。为了确定这两个队列之间的基因组差异,我们对 30 名北美 ATLL 患者进行了靶向外显子测序,并将结果与日本 ATLL 病例进行了比较。虽然 TP53 突变的频率相当,但表观遗传和组蛋白修饰基因(57%)的突变频率明显更高,而 JAK/STAT 和 T 细胞受体/NF-κB 通路基因的突变频率明显更低。最常见的表观遗传突变类型是影响 EP300(20%)的突变。作为一个类别,表观遗传突变与不良预后相关。对 9 个原发性患者样本进行 RNA 测序分析也揭示了与日本病例的不同之处。具有突变 EP300 基因的 ATLL 样本中总蛋白和乙酰化 p53 蛋白减少,转录特征类似于 p53 突变型癌症。最重要的是,地西他滨在 EP300 突变的 ATLL 样本中具有高度选择性的单一药物活性,表明地西他滨治疗在 EP300 突变的 ATLL 细胞中诱导合成致死表型。总之,我们证明了北美 ATLL 具有独特的基因组景观,其特征是频繁发生表观遗传突变,这些突变可以通过 DNA 甲基转移酶抑制剂进行临床前靶向治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ba9/6410908/161a4d25339a/blood824607absf1.jpg

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