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CXCL1 和 CXCL6 是 HCC 对 TACE 反应的潜在预测因子。

CXCL1 and CXCL6 Are Potential Predictors for HCC Response to TACE.

机构信息

Department of Internal Medicine I, University Hospital Frankfurt, Goethe University-Frankfurt am Main, 60590 Frankfurt am Main, Germany.

Dr. Senckenberg Institute for Pathology, University Hospital Frankfurt, Goethe University Frankfurt am Main, 60590 Frankfurt am Main, Germany.

出版信息

Curr Oncol. 2023 Mar 20;30(3):3516-3528. doi: 10.3390/curroncol30030267.

Abstract

Distinct immune patterns of hepatocellular carcinoma (HCC) may have prognostic implications in the response to transarterial chemoembolization (TACE). Thus, we aimed to exploratively analyze tumor tissue of HCC patients who do or do not respond to TACE, and to identify novel prognostic biomarkers predictive of response to TACE. We retrospectively included 15 HCC patients who had three consecutive TACE between January 2019 and November 2019. Eight patients had a response while seven patients had no response to TACE. All patients had measurable disease according to mRECIST. Corresponding tumor tissue samples were processed for differential expression profiling using NanoString nCounter PanCancer immune profiling panel. Immune-related pathways were broadly upregulated in TACE responders. The top differentially regulated genes were the upregulated CXCL1 (log2fc 4.98, Benjamini-Hochberg (BH)- < 0.001), CXCL6 (log2fc 4.43, BH- = 0.016) and the downregulated MME (log2fc -4.33, BH- 0.001). CD8/T-regs was highly increased in responders, whereas the relative number of T-regs to tumor-infiltrating lymphocytes (TIL) was highly decreased. We preliminary identified CXCL1 and CXCL6 as candidate genes that might have the potential to serve as therapeutically relevant biomarkers in HCC patients. This might pave the way to improve patient selection for TACE in HCC patients beyond expert consensus.

摘要

肝细胞癌 (HCC) 的不同免疫模式可能对经动脉化疗栓塞 (TACE) 反应的预后有影响。因此,我们旨在探索性地分析对 TACE 有反应和无反应的 HCC 患者的肿瘤组织,并确定预测 TACE 反应的新的预后生物标志物。我们回顾性纳入了 2019 年 1 月至 2019 年 11 月期间连续接受三次 TACE 的 15 例 HCC 患者。8 例患者对 TACE 有反应,7 例患者无反应。所有患者均根据 mRECIST 有可测量的疾病。用 NanoString nCounter PanCancer 免疫谱分析试剂盒对相应的肿瘤组织样本进行差异表达谱分析。TACE 应答者的免疫相关途径广泛上调。差异调节基因中,上调最明显的是 CXCL1(log2fc4.98,BH-<0.001)、CXCL6(log2fc4.43,BH-=0.016)和下调最明显的 MME(log2fc-4.33,BH-0.001)。应答者中 CD8/T-regs 高度增加,而 T 调节细胞与肿瘤浸润淋巴细胞 (TIL) 的相对数量显著减少。我们初步确定 CXCL1 和 CXCL6 为候选基因,它们可能有潜力作为 HCC 患者治疗相关的生物标志物。这可能为改善 HCC 患者 TACE 患者选择提供新的途径,超越专家共识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7489/10046993/7de5fc3998c0/curroncol-30-00267-g001.jpg

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