LRRC3-DT Inhibits Malignant Behaviors of Hepatocellular Carcinoma and is Associated With CCDC81 Expression.

IF 3.1 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jinglu Li, Yunfeng Luo, Mei Luo, Zhiqiang Yue, Liuxia Yuan, Huixuan Wang, Lin Chen, Linling Ju
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引用次数: 0

Abstract

Background: Enhancer RNAs (eRNAs) are important regulators of tumor development and progression. Nevertheless, the diagnostic utility of circulating eRNAs in hepatocellular carcinoma (HCC) remains unclear.

Methods: This was a retrospective study. The recently identified eRNA, leucine-rich repeat-containing 3 divergent transcript (LRRC3-DT), was analyzed in serum samples, tissue specimens, and various cell lines. Its diagnostic performance was evaluated alone and in combination with alpha-fetoprotein (AFP) and protein induced by vitamin K absence or antagonist-II (PIVKA-II) using receiver operating characteristic (ROC) curve analysis. Functional investigations were performed to assess the biological role of LRRC3-DT by overexpressing and knocking down this eRNA in HCC cell lines. Furthermore, using transcriptome sequencing, potential target genes of LRRC3-DT were identified.

Results: The serum levels of LRRC3-DT were significantly lower in patients diagnosed with HCC than in healthy controls. When LRRC3-DT was assessed alongside AFP and PIVKA-II, the combination improved sensitivity for the detection of HCC. Despite earlier research indicating that LRRC3-DT is present primarily in the nucleus and is strongly associated with tumor proliferation, invasion, and apoptosis, the serum levels of LRRC3-DT were similar between patients with HCC and those with benign liver diseases in the present study. These findings indicate limited specificity in distinguishing between these two conditions.

Conclusions: Serum LRRC3-DT represents a potential auxiliary biomarker for early HCC screening; its combined use with other indicators improved diagnostic performance. However, it cannot individually discriminate HCC from benign liver disorders, and additional validation studies are warranted to confirm its differential diagnostic value.

LRRC3-DT抑制肝细胞癌恶性行为并与CCDC81表达相关
背景:增强子rna (Enhancer RNAs, eRNAs)是肿瘤发生和发展的重要调控因子。然而,循环erna在肝细胞癌(HCC)诊断中的应用仍不清楚。方法:回顾性研究。最近发现的eRNA,富含亮氨酸的重复-含有3发散转录物(LRRC3-DT),在血清样本、组织标本和各种细胞系中进行了分析。采用受试者工作特征(ROC)曲线分析,评价其单独或与甲胎蛋白(AFP)和维生素K缺失或拮抗剂- ii (PIVKA-II)诱导的蛋白(PIVKA-II)联合的诊断性能。通过在HCC细胞系中过表达和敲低LRRC3-DT的功能研究来评估其生物学作用。此外,通过转录组测序,鉴定了LRRC3-DT的潜在靶基因。结果:HCC患者血清LRRC3-DT水平明显低于健康对照组。当LRRC3-DT与AFP和PIVKA-II联合评估时,该组合提高了检测HCC的敏感性。尽管早期研究表明LRRC3-DT主要存在于细胞核中,并与肿瘤增殖、侵袭和凋亡密切相关,但在本研究中,HCC患者和良性肝病患者的血清LRRC3-DT水平相似。这些发现表明区分这两种疾病的特异性有限。结论:血清LRRC3-DT是早期HCC筛查的潜在辅助生物标志物;它与其他指标的结合使用提高了诊断性能。然而,它不能单独区分HCC和良性肝脏疾病,需要进一步的验证研究来确认其鉴别诊断价值。
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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