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EGR1 作为结外 NK/T 细胞淋巴瘤预后的潜在标志物。

EGR1 as a potential marker of prognosis in extranodal NK/T-cell lymphoma.

机构信息

Division of Hematology-Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.

Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Sci Rep. 2021 May 14;11(1):10342. doi: 10.1038/s41598-021-89754-8.

DOI:10.1038/s41598-021-89754-8
PMID:33990633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8121831/
Abstract

Extranodal natural killer T-cell lymphoma (ENKTL) is an aggressive malignancy with a dismal prognosis. In the present study, gene expression profiling was performed to provide more information on ENKTL molecular signature and offer a rationale for further investigation of prognostic markers in ENKTL. NanoString nCounter Analysis encompassing 133 target genes was used to compare gene expression levels of 43 ENKTL tumor samples. The majority of the patients were under 60 years of age (79.1%); 32 (74.4%) patients had nasal type ENKTL and 23 patients (53.5%) had intermediate/high risk ENKTL based on the prognostic index for natural killer cell lymphoma (PINK). The median follow-up was 15.9 months and the median overall survival (OS) was 16.1 months (95% CI 13.0-69.8). EGR1 upregulation was consistently identified in the localized stage with a low risk of prognostic index based on the PINK. Among the six significantly relevant genes for EGR1 expression, high expression levels of genes, including CD59, GAS1, CXCR7, and RAMP3, were associated with a good survival prognosis. The in vitro test showed EGR1 modulated the transcriptional activity of the target genes including CD59, GAS1, CXCR7, and RAMP3. Downregulation of EGR1 and its target genes significantly inhibited apoptosis and decreased chemosensitivity and attenuated radiation-induced apoptosis. The findings showed EGR1 may be a candidate for prognostic markers in ENKTL. Considerable additional characterization may be necessary to fully understand EGR1.

摘要

结外自然杀伤/T 细胞淋巴瘤(ENKTL)是一种侵袭性恶性肿瘤,预后较差。本研究通过基因表达谱分析,为 ENKTL 的分子特征提供更多信息,并为进一步研究 ENKTL 的预后标志物提供理论依据。采用包含 133 个靶基因的 NanoString nCounter 分析,比较了 43 例 ENKTL 肿瘤样本的基因表达水平。大多数患者年龄在 60 岁以下(79.1%);32 例(74.4%)患者为鼻型 ENKTL,23 例(53.5%)患者根据自然杀伤细胞淋巴瘤预后指数(PINK)为中高危。中位随访时间为 15.9 个月,中位总生存期(OS)为 16.1 个月(95%CI 13.0-69.8)。在基于 PINK 的局部阶段和低风险预后指数中,一致发现 EGR1 上调。在与 EGR1 表达相关的 6 个显著相关基因中,包括 CD59、GAS1、CXCR7 和 RAMP3 在内的基因高表达与良好的生存预后相关。体外试验表明,EGR1 调节了 CD59、GAS1、CXCR7 和 RAMP3 等靶基因的转录活性。EGR1 及其靶基因的下调显著抑制了细胞凋亡,降低了化疗敏感性,并减弱了辐射诱导的细胞凋亡。这些发现表明,EGR1 可能是 ENKTL 的候选预后标志物。为了充分了解 EGR1,可能还需要进行更多的特征描述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/91fddd477b16/41598_2021_89754_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/72ffacb42108/41598_2021_89754_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/392b3f8fbc3a/41598_2021_89754_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/0a1c94f6a9dd/41598_2021_89754_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/91fddd477b16/41598_2021_89754_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/72ffacb42108/41598_2021_89754_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/d152e272a2c1/41598_2021_89754_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/875b79785fe2/41598_2021_89754_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/adb4865e6acc/41598_2021_89754_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/392b3f8fbc3a/41598_2021_89754_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/0a1c94f6a9dd/41598_2021_89754_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/8121831/91fddd477b16/41598_2021_89754_Fig7_HTML.jpg

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