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原发性玻璃体视网膜淋巴瘤的基因表达谱分析。

Gene expression profiling of primary vitreoretinal lymphoma.

机构信息

Department of Hematological Therapeutics, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.

Division of Hematology and Oncology, Department of Internal Medicine, St. Marianna University School of Medicine, Kanagawa, Japan.

出版信息

Cancer Sci. 2020 Apr;111(4):1417-1421. doi: 10.1111/cas.14347. Epub 2020 Mar 12.

Abstract

The characteristics of tumor cells of primary vitreoretinal lymphoma (PVRL) have not been defined, although researches have shown that most cases are of diffuse large B-cell lymphoma (DLBCL). To determine the subtype and biological characteristics of tumor cells of PVRL, we performed a gene expression profiling analysis. RNA was extracted from the vitreous fluid of 7 PVRL patients and from nodal samples of 10 DLBCL patients: 6 of germinal center B-cell (GCB) type and 4 of activated B-cell (ABC) type determined by Hans' criteria. Six PVRL samples showed gene expression profiles that were similar to each other. The patterns were different from those of the ABC-type nodular DLBCL but relatively close to those of the GCB-type nodular DLBCL. Interestingly, all of the 6 examined PVRL samples had either MYD88 or mutation in the immunoreceptor tyrosine-based activation motif (ITAM) region of CD79B. Five PVRL patients with similar gene expression profiles were treated with a standardized regimen: intravitreal administration of methotrexate (MTX) followed by six courses of systemic high doses of MTX. As a result, 2 patients had CD79B mutations and showed early central nervous system (CNS) progression. Patients without CNS progression did not have this mutation. In conclusion, PVRL had unique genetic features: an expression pattern different from ABC-type and relatively close to GCB-type DLBCL. CD79B mutations showed potential to serve as prognostic markers for CNS progression.

摘要

原发性玻璃体内视网膜淋巴瘤 (PVRL) 的肿瘤细胞特征尚未确定,尽管研究表明大多数病例为弥漫性大 B 细胞淋巴瘤 (DLBCL)。为了确定 PVRL 肿瘤细胞的亚型和生物学特征,我们进行了基因表达谱分析。从 7 例 PVRL 患者的玻璃体液和 10 例 DLBCL 患者的淋巴结样本中提取 RNA:6 例符合 Hans 标准的生发中心 B 细胞 (GCB) 型,4 例为激活 B 细胞 (ABC) 型。6 例 PVRL 样本的基因表达谱彼此相似。这些模式与 ABC 型结节性 DLBCL 不同,但与 GCB 型结节性 DLBCL 较为接近。有趣的是,所有 6 例检查的 PVRL 样本均存在 MYD88 或 CD79B 免疫受体酪氨酸激活基序 (ITAM) 区突变。5 例具有相似基因表达谱的 PVRL 患者接受了标准化治疗方案:玻璃体内注射甲氨蝶呤 (MTX) ,随后进行 6 个疗程的全身高剂量 MTX。结果,2 例患者存在 CD79B 突变,表现为早期中枢神经系统 (CNS) 进展。没有 CNS 进展的患者没有这种突变。总之,PVRL 具有独特的遗传特征:表达模式不同于 ABC 型,与 GCB 型 DLBCL 较为接近。CD79B 突变可能成为 CNS 进展的预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7062/7156859/e4dd220a72a1/CAS-111-1417-g001.jpg

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