Expression and clinical significance of NLRC5 in hepatocellular carcinoma.

IF 4.4 4区 医学 Q2 ONCOLOGY Cancer Biology & Therapy Pub Date : 2024-12-31 Epub Date: 2024-08-12 DOI:10.1080/15384047.2024.2390205
Xiangyu Ma, Shangkun Ning, Tong Sun, Mei Liu, Jibing Liu
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Abstract

NLRC5, the largest member of the nucleotide-binding and oligomerization domain (NOD)-like receptor (NLR) family, has been reported to participate in the regulation of immune function and is associated with chronic inflammatory diseases. However, the biological function of NLRC5 in hepatocellular carcinoma (HCC) has not been fully demonstrated. The aim of this study is to evaluate NLRC5 expression in the tumor tissues of HCC patients undergoing surgical treatment, assess its prognostic value, and explore its relationship with critical immune-related molecules within the tumor microenvironment. A total of 100 patients with hepatitis B virus-associated HCC receiving surgical treatment were enrolled in the study. Immunohistochemical results were obtained by scoring the intensity of cellular staining and the percentage of positive cells in the tissue sections. The association between NLRC5 expression levels and the main clinicopathological factors was analyzed by Chi-square test method. The prognostic values were analyzed by COX regression model and the Kaplan-Meier survival curve. Receiver operating characteristic (ROC) curve analysis was performed to assess the predictive performance of NLRC5 in postoperative patients with HCC. IHC showed that high expression of NLRC5 was observed in 67% of HCC tissue samples. Chi-square test showed that NLRC5 was a risk factor associated with tumor number, satellite nodule, and envelope invasion. Kaplan-Meier survival curves and COX survival analysis showed that high expression of NLRC5 was significantly associated with decreased overall survival (OS) in HCC patients (HR = 1.79, 95% CI 1.03-3.12, p = .041). However, univariate logistic regression analysis revealed that NLRC5 showed positive relationship with GZMB and CD8α suggesting its role in immune escape of HCC. ROC curve analysis showed that the combination of tumor number, envelope invasion, and NLRC5 expression (area under the curve = 0.824, sensitivity = 77.30%, specificity = 82.4%) can more accurately evaluate the prognosis of HCC patients compared to the combination of only tumor number and envelope invasion (area under the curve = 0.690, sensitivity = 43.9%, specificity = 94.1%).NLRC5 plays a crucial role in progression of HCC and can be considered as a potential prognostic and predictive biomarker. Targeting NLRC5 may provide an attractive therapeutic approach for HCC.

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肝细胞癌中 NLRC5 的表达和临床意义。
NLRC5是核苷酸结合和寡聚化结构域(NOD)样受体(NLR)家族中最大的成员,据报道它参与调节免疫功能,并与慢性炎症性疾病相关。然而,NLRC5 在肝细胞癌(HCC)中的生物学功能尚未得到充分证实。本研究旨在评估接受手术治疗的 HCC 患者肿瘤组织中 NLRC5 的表达,评估其预后价值,并探讨其与肿瘤微环境中关键免疫相关分子的关系。研究共纳入了100名接受手术治疗的乙肝病毒相关性HCC患者。通过对组织切片中的细胞染色强度和阳性细胞百分比进行评分,得出免疫组化结果。NLRC5表达水平与主要临床病理因素之间的关系采用Chi-square检验法进行分析。预后值通过 COX 回归模型和 Kaplan-Meier 生存曲线进行分析。为评估 NLRC5 对术后 HCC 患者的预测能力,进行了接收者操作特征(ROC)曲线分析。IHC显示,在67%的HCC组织样本中观察到NLRC5的高表达。卡普兰-梅耶生存曲线(Kaplan-Meier survival curve)显示,NLRC5是与肿瘤数量、卫星结节和包膜侵犯相关的风险因素。卡普兰-梅耶生存曲线和 COX 生存分析表明,NLRC5 的高表达与 HCC 患者总生存期(OS)的降低显著相关(HR = 1.79,95% CI 1.03-3.12,p = .041)。然而,单变量逻辑回归分析显示,NLRC5与GZMB和CD8α呈正相关,表明其在HCC免疫逃逸中的作用。ROC曲线分析表明,肿瘤数目、包膜侵犯和NLRC5表达的组合(曲线下面积=0.824,灵敏度=77.30%,特异度=82.4%)与仅有肿瘤数目和包膜侵犯的组合(曲线下面积=0.690,灵敏度=43.9%,特异度=94.1%)相比,能更准确地评估HCC患者的预后。靶向 NLRC5 可为 HCC 提供一种有吸引力的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer Biology & Therapy
Cancer Biology & Therapy 医学-肿瘤学
CiteScore
7.00
自引率
0.00%
发文量
60
审稿时长
2.3 months
期刊介绍: Cancer, the second leading cause of death, is a heterogenous group of over 100 diseases. Cancer is characterized by disordered and deregulated cellular and stromal proliferation accompanied by reduced cell death with the ability to survive under stresses of nutrient and growth factor deprivation, hypoxia, and loss of cell-to-cell contacts. At the molecular level, cancer is a genetic disease that develops due to the accumulation of mutations over time in somatic cells. The phenotype includes genomic instability and chromosomal aneuploidy that allows for acceleration of genetic change. Malignant transformation and tumor progression of any cell requires immortalization, loss of checkpoint control, deregulation of growth, and survival. A tremendous amount has been learned about the numerous cellular and molecular genetic changes and the host-tumor interactions that accompany tumor development and progression. It is the goal of the field of Molecular Oncology to use this knowledge to understand cancer pathogenesis and drug action, as well as to develop more effective diagnostic and therapeutic strategies for cancer. This includes preventative strategies as well as approaches to treat metastases. With the availability of the human genome sequence and genomic and proteomic approaches, a wealth of tools and resources are generating even more information. The challenge will be to make biological sense out of the information, to develop appropriate models and hypotheses and to translate information for the clinicians and the benefit of their patients. Cancer Biology & Therapy aims to publish original research on the molecular basis of cancer, including articles with translational relevance to diagnosis or therapy. We will include timely reviews covering the broad scope of the journal. The journal will also publish op-ed pieces and meeting reports of interest. The goal is to foster communication and rapid exchange of information through timely publication of important results using traditional as well as electronic formats. The journal and the outstanding Editorial Board will strive to maintain the highest standards for excellence in all activities to generate a valuable resource.
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