Osaka Iseikai Clinic for Cancer Therapy, Iseikai Holonics Group, Osaka, Japan.
Laboratory of Molecular Target Therapy for Cancer, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Sci Rep. 2020 May 21;10(1):8435. doi: 10.1038/s41598-020-65463-6.
Primary central nervous system lymphoma (PCNSL) is a brain malignant non-Hodgkin's B-cell lymphoma. The standard treatments are high-dose methotrexate (MTX)-based chemotherapies and deferred whole brain radiotherapy. However, MTX resistance-dependent global expression and signaling pathway changes and their relationship with prognoses have not yet been elucidated. Here, we conducted a global expression analysis with next-generation sequencing and gene set enrichment analysis (GSEA) in MTX-resistant PCNSL cell lines (HKBML-MTX and TK-MTX) and PCNSL tissues. In rank scores, genes listed in HKBML-MTX and TK-MTX were enriched in PCNSL with poor prognoses. In fold changes, a part of differentially-expressed genes in PCNSL tissues were also detected in HKBML-MTX and TK-MTX cells; FOXD2-AS1 and MMP19 were commonly expressed in both HKBML-MTX and TK-MTX, FABP5 and CD70 were HKBML-MTX-specifically expressed, and CLCN2, HOXB9, INE1, and LRP5L were TK-MTX-specifically expressed, which may provide a combination of prognostic markers on MTX-sensitivities in PCNSL. Additionally, PCNSL subgroups, divided with hierarchical clustering and Kaplan-Meier methods, included twenty commonly expressed genes in both HKBML-MTX and TK-MTX, ten HKBML-MTX-specifically expressed genes, and two TK-MTX-specifically expressed genes. These results suggest that the GSEA-assisted gene signatures can provide a combination for prognostic markers in recurrent PCNSL with MTX resistances.
原发性中枢神经系统淋巴瘤(PCNSL)是一种脑恶性非霍奇金 B 细胞淋巴瘤。标准治疗方法是大剂量甲氨蝶呤(MTX)为基础的化疗和延迟全脑放疗。然而,MTX 耐药相关的全表达和信号通路变化及其与预后的关系尚未阐明。在这里,我们通过下一代测序和基因集富集分析(GSEA)对 MTX 耐药 PCNSL 细胞系(HKBML-MTX 和 TK-MTX)和 PCNSL 组织进行了全表达分析。在秩评分中,HKBML-MTX 和 TK-MTX 中列出的基因在预后不良的 PCNSL 中富集。在 fold change 方面,PCNSL 组织中部分差异表达基因也在 HKBML-MTX 和 TK-MTX 细胞中检测到;FOXD2-AS1 和 MMP19 在 HKBML-MTX 和 TK-MTX 中均有表达,FABP5 和 CD70 仅在 HKBML-MTX 中表达,CLCN2、HOXB9、INE1 和 LRP5L 仅在 TK-MTX 中表达,这可能为 PCNSL 中 MTX 敏感性提供了一组预后标志物。此外,通过层次聚类和 Kaplan-Meier 方法对 PCNSL 亚组进行划分,包含了在 HKBML-MTX 和 TK-MTX 中均有表达的 20 个共同表达基因、10 个 HKBML-MTX 特异性表达基因和 2 个 TK-MTX 特异性表达基因。这些结果表明,GSEA 辅助基因特征可提供一组复发性 PCNSL 中 MTX 耐药的预后标志物。