Primary liver cancer

原发性肝癌
  • 文章类型: Journal Article
    背景:原发性肝细胞癌(HCC)的发病率和死亡率很高,常规治疗是射频消融术(RFA)联合肝动脉化疗栓塞术(TACE);3年生存率仍然很低。Further,没有有效预测其预后的视觉方法。
    目的:探讨RFA和TACE治疗后影响HCC预后的因素,建立列线图预测模型。
    方法:回顾性收集并记录杭州临平中医医院2020年5月至2022年12月采用RFA和TACE治疗的150例HCC患者的临床及随访资料。我们使用多变量逻辑回归检查了他们的预后因素,并使用R软件(4.1.2版)创建了列线图预后预测模型。使用自举技术进行内部验证。使用一致性指数(CI)评估列线图预测模型的预后效果,校正曲线,和接收器工作特性曲线。
    结果:在接受RFA和TACE治疗的150例患者中,92例(61.33%)发生复发和转移。Logistic回归分析确定了六个变量,并创建了预测模型。模型内部验证结果显示aCI为0.882。预后预测模型的校正曲线趋势始终在对角线附近,内部验证前后的平均绝对误差为0.021。内部验证后预测模型的曲线下面积为0.882[95%置信区间(95CI):0.820-0.945],特异性为0.828,敏感性为0.656。根据Hosmer-Lemeshow测试,χ2=3.552,P=0.895。预测模型证明了令人满意的校准,决策曲线分析证明了其临床适用性。
    结论:肝癌患者行RFA和TACE后的预后受多种因素影响。建立的基于影响参数的预测模型显示出良好的预后预测效能。
    BACKGROUND: The incidence and mortality rates of primary hepatocellular carcinoma (HCC) are high, and the conventional treatment is radiofrequency ablation (RFA) with transcatheter arterial chemoembolization (TACE); however, the 3-year survival rate is still low. Further, there are no visual methods to effectively predict their prognosis.
    OBJECTIVE: To explore the factors influencing the prognosis of HCC after RFA and TACE and develop a nomogram prediction model.
    METHODS: Clinical and follow-up information of 150 patients with HCC treated using RFA and TACE in the Hangzhou Linping Hospital of Traditional Chinese Medicine from May 2020 to December 2022 was retrospectively collected and recorded. We examined their prognostic factors using multivariate logistic regression and created a nomogram prognosis prediction model using the R software (version 4.1.2). Internal verification was performed using the bootstrapping technique. The prognostic efficacy of the nomogram prediction model was evaluated using the concordance index (CI), calibration curve, and receiver operating characteristic curve.
    RESULTS: Of the 150 patients treated with RFA and TACE, 92 (61.33%) developed recurrence and metastasis. Logistic regression analysis identified six variables, and a predictive model was created. The internal validation results of the model showed a CI of 0.882. The correction curve trend of the prognosis prediction model was always near the diagonal, and the mean absolute error before and after internal validation was 0.021. The area under the curve of the prediction model after internal verification was 0.882 [95% confidence interval (95%CI): 0.820-0.945], with a specificity of 0.828 and sensitivity of 0.656. According to the Hosmer-Lemeshow test, χ 2 = 3.552 and P = 0.895. The predictive model demonstrated a satisfactory calibration, and the decision curve analysis demonstrated its clinical applicability.
    CONCLUSIONS: The prognosis of patients with HCC after RFA and TACE is affected by several factors. The developed prediction model based on the influencing parameters shows a good prognosis predictive efficacy.
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  • 文章类型: Journal Article
    原发性肝癌(PLC)是世界范围内最常见的胃肠道恶性肿瘤之一。受限于肝移植供体的短缺和肿瘤的异质性,肝癌患者缺乏有效的治疗选择,导致快速进展和转移。目前,PLC的临床前模型达不到临床现实,并且在对疾病进展和药物治疗有效性的反应方面受到限制。类器官是体外三维培养的临床前模型,具有高度异质性,可保留原发性肿瘤的组织形态学和基因组特征。肝癌类器官已广泛用于药物筛选,新的目标发现,和精准医学;因此代表了研究PLC的一个有前途的工具。这里,我们总结了肝癌类器官的研究进展及其作为疾病模型的潜在应用。本综述对这一新兴技术进行了全面介绍,为研究者在精准医学领域的探索提供了新的思路。
    Primary liver cancer (PLC) is one of the most common malignant gastrointestinal tumors worldwide. Limited by the shortage of liver transplantation donors and the heterogeneity of tumors, patients with liver cancer lack effective treatment options, which leads to rapid progression and metastasis. Currently, preclinical models of PLC fall short of clinical reality and are limited in their response to disease progression and the effectiveness of drug therapy. Organoids are in vitro three-dimensional cultured preclinical models with a high degree of heterogeneity that preserve the histomorphological and genomic features of primary tumors. Liver cancer organoids have been widely used for drug screening, new target discovery, and precision medicine; thus representing a promising tool to study PLC. Here, we summarize the progress of research on liver cancer organoids and their potential application as disease models. This review provides a comprehensive introduction to this emerging technology and offers new ideas for researchers to explore in the field of precision medicine.
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  • 文章类型: Journal Article
    背景:复方斑茅胶囊(FFBM),中药,多年来一直被用于治疗原发性肝癌(PLC)。然而,生物活性成分,FFBM治疗PLC的机制尚不清楚。我们的目标是利用网络药理学来研究这些方面,并随后通过临床数据验证其有效性。
    方法:从HERB数据库获得FFBM成分,并使用SwissTargetPrediction数据库筛选生物活性成分。PharmMapper和GEO数据库用于获取FFBM和PLC的靶标和差异表达基因(DEGs),分别。使用维恩图确定了常见目标,然后进行富集和蛋白质-蛋白质相互作用(PPI)分析。此外,利用Cytoscape软件鉴定Hub基因并构建成分靶途径网络。随后,回顾性收集2008年1月至2019年12月在我院接受肝动脉化疗栓塞(TACE)治疗的确诊为不可切除PLC的患者.最后,进行Cox分析以揭示FFBM在不可切除的PLC的治疗中的作用。
    结果:FFBM有232个目标,PLC有1582个DEG。HSP90AA1和SRC被确定为关键靶标。阿尔法-桑他洛尔,甘草酸,和莫罗尼甙被确定为前三种生物活性成分。富集分析揭示了FFBM用于治疗PLC与多种途径之间的显着联系,如化学致癌作用,PI3K-AKT,Rap1,FoxO,MAPK,和VEGF途径。临床数据显示,食用FFBM可显着改善不可切除的PLC的预后,风险比为0.69。
    结论:我们的研究确定了FFBM的生物活性成分及其治疗PLC的潜在机制。此外,我们通过临床数据验证了有效性.
    BACKGROUND: Fufang Banmao capsules (FFBM), a traditional Chinese medicine, has been used to treat primary liver cancer (PLC) for several years. However, the bioactive ingredients, and mechanism of FFBM for treating PLC remains unclear. Our objective is to utilize network pharmacology to investigate these aspects and subsequently validate their effectiveness through clinical data.
    METHODS: The FFBM ingredients were obtained from the HERB database and screened for bioactive ingredients using the SwissTargetPrediction database. The PharmMapper and GEO database were used to acquire targets and differentially expressed genes (DEGs) for FFBM and PLC, respectively. Common targets were identified using Venn diagrams, followed by enrichment and protein-protein interaction (PPI) analysis. Furthermore, the Cytoscape software was utilized to identify Hub genes and construct the ingredienttarget- pathway network. Subsequently, patients diagnosed with unresectable PLC who underwent transcatheter arterial chemoembolization (TACE) at our hospital between January 2008 and December 2019 were retrospectively collected. Finally, Cox analysis was conducted to reveal the role of FFBM in the treatment of unresectable PLC.
    RESULTS: FFBM had 232 targets, and PLC had 1582 DEGs. HSP90AA1 and SRC were identified as crucial targets. Alpha-santalol, glycyrrhizin, and morroniside were identified as the top three bioactive ingredients. Enrichment analysis revealed a significant connection between FFBM utilization for treating PLC and multiple pathways, such as chemical carcinogenesis, PI3K-AKT, Rap1, FoxO, MAPK, and VEGF pathway. Clinic data revealed that consuming FFBM significantly improved the prognosis of unresectable PLC with a hazard ratio of 0.69.
    CONCLUSIONS: Our study identified the bioactive ingredients of FFBM and its potential mechanisms for treating PLC. Additionally, we validated the effectiveness through clinical data.
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  • 文章类型: Journal Article
    Hedgehog(Hh)信号通路失调与代谢功能障碍相关脂肪性肝炎的发病机制有关,和声波Hh(SHh)蛋白,Hh通路中的一个关键分子,在膨胀的肝细胞中表达。本研究旨在探讨SHh在脂肪性肝细胞癌(SH-HCC)中的表达及其临床病理意义。采用逆转录-定量聚合酶链反应和免疫组织化学方法检测SH-HCC中SHh基因和SHh蛋白的表达。此外,将常规HCC(C-HCC)患者纳入对照组.还进行了患者和肿瘤特征的比较。在整个队列中,SH-HCC的患病率为3%,它与糖尿病的高患病率显著相关。在所有SH-HCC患者中均检测到SHhmRNA,但在23%的C-HCC患者中没有。值得注意的是,SHhmRNA表达在SH-HCC患者和C-HCC患者之间没有显着差异;然而,SH-HCC患者的SHh蛋白高表达明显高于C-HCC患者。尽管SH-HCC和C-HCC组之间的预后没有显着差异,SHh蛋白高表达是HCC的独立不良预后因素。总之,SHh可能作为肝癌患者的治疗靶点。
    Hedgehog (Hh) signaling pathway dysregulation is involved in the pathogenesis of metabolic dysfunction-associated steatohepatitis, and the sonic Hh (SHh) protein, a pivotal molecule in the Hh pathway, is expressed in ballooned hepatocytes. The present study aimed to investigate the clinicopathological significance of SHh expression in steatohepatitic hepatocellular carcinoma (SH-HCC). Reverse transcription-quantitative polymerase chain reaction and immunohistochemistry were performed to examine SHh gene and SHh protein expression in SH-HCC. Additionally, patients with conventional HCC (C-HCC) were included in the control group. Comparisons of patient and tumor characteristics were also performed. The prevalence of SH-HCC was 3% in the whole cohort, and it was significantly associated with a high prevalence of diabetes mellitus. SHh mRNA was detected in all patients with SH-HCC, but not in 23% of patients with C-HCC. Notably, SHh mRNA expression was not significantly different between patients with SH-HCC and those with C-HCC; however, high SHh protein expression was significantly more frequent in SH-HCC patients than in those with C-HCC. Although the prognosis was not significantly different between the SH-HCC and C-HCC groups, high SHh protein expression was an independent poor prognostic factor for HCC. In conclusion, SHh could potentially serve as a therapeutic target for patients with HCC.
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  • 文章类型: Journal Article
    目的:探讨肝动脉介入栓塞化疗(TACE)治疗原发性肝癌的临床效果。
    方法:选择2017年1月至2018年1月我院收治的73例PHC患者,采用随机数字表法分为研究组37例和对照组36例。对照组仅接受超声引导下的微波消融治疗,研究组在对照组基础上术前再次行TACE治疗。癌抗原125(CA125)的表达水平,甲胎蛋白(AFP),多种肿瘤抑制因子1(P16)蛋白,治疗后不同时间段比较两组患者癌抗原19-9(CA19-9),和缓解率(ORR),控制率(DCR),比较两组治疗后3个月的并发症发生率和治疗后3年的生存率。
    结果:治疗1年后,ORR,DCR,研究组P16蛋白水平高于对照组(P<0.05),差异有统计学意义;研究组CA125、CA19-9、AFP水平低于对照组(P<0.05),差异有统计学意义。回归方程显示,两组患者的长期生存率均随时间呈下降趋势,研究组的长期生存率始终高于对照组。
    结论:原发性肝癌患者肝动脉介入化疗栓塞的综合干预效果更好,能有效降低患者并发症和不良反应的发生率,有利于缩短患者肝动脉介入化疗栓塞治疗时间。
    OBJECTIVE: To investigate clinical effects of hepatic artery interventional embolization chemotherapy (TACE) for primary hepatocellular carcinoma (PHC).
    METHODS: 73 patients with PHC in our hospital from January 2017 to January 2018 were selected and divided into 37 cases in study group and 36 cases in control group by random number table method. The control group received only ultrasound-guided microwave ablation treatment, and the study group received TACE treatment again before surgery based on control group. The expression levels of cancer antigen 125 (CA125), alpha-fetoprotein (AFP), multiple tumor suppressors 1 (P16) proteins, and cancer antigen 19-9 (CA19-9) were compared between the two groups at different time periods after treatment, and the remission rate (ORR), control rate (DCR), complication rate at 3 months after treatment and survival rate at 3 years after treatment were compared.
    RESULTS: After 1 year of treatment, ORR, DCR, and P16 protein levels in the study group were higher than those in the control group (P < 0.05), and differences were statistically significant; CA125, CA19-9, and AFP levels in study group were lower than those in the control group (P < 0.05), and differences were statistically significant. The regression equation showed that long-term survival rate of both groups showed decreasing trend over time, while long-term survival rate of study group was always higher than that of the control group.
    CONCLUSIONS: Comprehensive intervention for hepatic artery interventional chemoembolization in patients with primary hepatocellular carcinoma is more effective, which can effectively reduce incidence of complications and adverse effects in patients and help shorten treatment time of hepatic artery interventional chemoembolization in patients.
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  • 文章类型: Journal Article
    胆管细胞癌(CCA)是第二常见的原发性肝癌,随着全球发病率的增加和治疗选择的不足。肝内和肝外胆管有明显不同的胚胎起源和发育行为,因此,肝内和肝外CCA(ICC与ECC)在分子上是不同的。肿瘤治疗中一个有希望的策略是靶向治疗,靶向调节细胞存活和增殖的蛋白质,如MAPK/ERK和PI3K/AKT/mTOR信号通路。先前已经在CCA细胞系中测试了这些途径的抑制剂。然而,这些细胞系不能明确地分配给ICC或ECC,结果表明,通过靶向治疗诱导细胞凋亡。我们测试了靶向疗法(司米替尼,MK2206)在三种定义的ICC细胞系(HuH28,RBE,SSP25)。我们观察到两种途径双重抑制的累加效应,根据抑制磷酸-AKT和磷酸-ERK1/2的表达。双重抑制比每个单一抑制更有效地阻断增殖,但细胞数量没有下降到基线以下。因此,我们观察到G1期停滞,但未观察到细胞凋亡或细胞死亡(通过裂解的caspase-3,AIFM1调节,次G0/G1阶段)。我们得出的结论是,MAPK/ERK和PI3K/AKT/mTOR通路的双重抑制对体外阻断ICC细胞系的增殖非常有效;然而,必须严格检查潜在的临床应用,作为增殖阻滞也可以诱导对标准疗法的抗性。
    Cholangiocellular carcinoma (CCA) is the second most common primary liver cancer, with increasing incidence worldwide and inadequate therapeutic options. Intra- and extrahepatic bile ducts have distinctly different embryonic origins and developmental behavior, and accordingly, intra- and extrahepatic CCAs (ICC vs. ECC) are molecularly different. A promising strategy in oncotherapy is targeted therapy, targeting proteins that regulate cell survival and proliferation, such as the MAPK/ERK and PI3K/AKT/mTOR signaling pathways. Inhibitors of these pathways have been tested previously in CCA cell lines. However, these cell lines could not be clearly assigned to ICC or ECC, and the results indicated apoptosis induction by targeted therapeutics. We tested targeted therapeutics (selumetinib, MK2206) in three defined ICC cell lines (HuH28, RBE, SSP25). We observed additive effects of the dual inhibition of the two pathways, in accordance with the inhibition of phospho-AKT and phospho-ERK1/2 expression. Proliferation was blocked more effectively with dual inhibition than with each single inhibition, but cell numbers did not drop below baseline. Accordingly, we observed G1 phase arrest but not apoptosis or cell death (measured by cleaved caspase-3, AIFM1 regulation, sub-G0/G1 phase). We conclude that the dual inhibition of the MAPK/ERK and PI3K/AKT/mTOR pathways is highly effective to block the proliferation of ICC cell lines in vitro; however, potential clinical applications must be critically examined, as a proliferation block could also induce resistance to standard therapies.
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  • 文章类型: Journal Article
    采用网络Meta分析和多标准决策分析(MCDA)模型对复方斑马龙胶囊的获益-风险进行评价。汇生口服液,和金龙胶囊辅助治疗原发性肝癌(PLC)。复方斑ataris胶囊的随机对照试验(RCT),汇生口服液,金龙胶囊治疗PLC的检索来自CNKI,万方,VIP,WebofScience,PubMed,科克伦图书馆采用R4.2进行网络荟萃分析,在此基础上通过间接比较获得了三种药物的作用值。基于收益-风险指数进行MCDA建立价值树。Hive3.2用于计算效益值,风险值,以及三种药物治疗PLC的获益风险值,并进行了敏感性分析,以评估结果的稳健性。采用OracleCrystalBall11.1对评价结果进行蒙特卡罗模拟优化。共纳入39项RCT。结果表明,复方斑潜鱼胶囊,汇生口服液,金龙胶囊联合肝动脉化疗栓塞术(TACE)的获益值分别为45、51和45,风险值分别为59、47和41,获益-风险值分别为52、49和43。复方Cantharis胶囊与回生口服液的获益-风险差异及[95CI]复方斑马龙胶囊vs金龙胶囊,汇生口服液与金龙胶囊的比较为3.00[-13.09,21.82],9.00[-4.39,24.62],和6.00[-8.84,20.28],分别。根据MCDA的结果,汇生口服液,金龙胶囊,复方斑ataris胶囊联合TACE治疗效果最大,最大的风险,和最佳的整体效益,分别。考虑到疗效和安全性,三种口服中成药联合TACE治疗PLC的优先顺序遵循复方斑ataris胶囊的趋势,汇生口服液,和金龙胶囊。
    Network Meta-analysis and multi-criteria decision analysis(MCDA) model were performed to evaluate the benefit-risk of Compound Cantharis Capsules, Huisheng Oral Solution, and Jinlong Capsules in the adjuvant treatment of primary liver cancer(PLC). The randomized controlled trial(RCT) of Compound Cantharis Capsules, Huisheng Oral Solution, and Jinlong Capsules in treating PLC were retrieved from CNKI, Wanfang, VIP, Web of Science, PubMed, and Cochrane Library. R 4.2 was employed to conduct a network Meta-analysis, on the basis of which the effect values of the three medicines were obtained by indirect comparison. MCDA was performed to establish the value tree based on the benefit-risk indexes. Hiview 3.2 was used to calculate the benefit values, risk values, and benefit-risk values of the three medicines in treating PLC, and a sensitivity analysis was carried out to evaluate the robustness of the results. Oracle Crystal Ball 11.1 was employed to optimize the evaluation results by Monte Carlo simulation. A total of 39 RCTs were included. The results showed that Compound Cantharis Capsules, Huisheng Oral Solution, and Jinlong Capsules combined with transcatheter arterial chemoembolization(TACE) had the benefit values of 45, 51 and 45, the risk values of 59, 47, and 41, and the benefit-risk values of 52, 49, and 43, respectively. The benefit-risk differences and [95%CI] of Compound Cantharis Capsules vs Huisheng Oral Solution, Compound Cantharis Capsules vs Jinlong Capsules, and Huisheng Oral Solution vs Jinlong Capsules were 3.00[-13.09, 21.82], 9.00[-4.39, 24.62], and 6.00[-8.84, 20.28], respectively. Based on the results of MCDA, Huisheng Oral Solution, Jinlong Capsules, and Compound Cantharis Capsules combined with TACE had the greatest benefit, the greatest risk, and the best overall benefit, respectively. Considering the efficacy and safety, the priority of the three oral Chinese patent medicines combined with TACE for treating PLC followed the trend of Compound Cantharis Capsules, Huisheng Oral Solution, and Jinlong Capsules.
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  • 文章类型: Journal Article
    原发性肝癌,更具体地说,肝细胞癌(HCC),仍然是一个与发病率和死亡率增加相关的重大全球健康问题。临床,生物,和分子异质性是众所周知的癌症的标志和肝癌被认为是最异质性的肿瘤类型之一,显示大量的患者间,肿瘤间和肿瘤内变异性。这种异质性在肝癌发生中起着关键作用,转移,复发和药物反应或耐药性。单峰单细胞测序技术已经彻底改变了我们对HCC肿瘤微环境中不同分子层次的理解。通过强调细胞异质性和癌症之间复杂的相互作用,治疗前和治疗期间的免疫和基质细胞,这些技术有助于更深入地理解肿瘤克隆性,血行扩散和免疫检查点抑制剂的作用机制。然而,主要问题仍有待阐明,鉴定预测对基于免疫治疗的方案的应答或抗性的生物标志物代表了重要的未满足的临床需求。尽管到目前为止,单细胞多组学在肝癌研究中的应用受到限制,只有在单细胞分辨率下,将各种单峰方法整合到多组学方法中,才能为HCC患者提供个性化护理的革命。在这次审查中,我们将重点介绍不同的已建立的单细胞测序技术,并探讨其对肝癌研究的生物学和临床影响,同时在这个充满活力和快速发展的领域中,对多维组学的未来作用一目了然。
    Primary liver cancer, more specifically hepatocellular carcinoma (HCC), remains a significant global health problem associated with increasing incidence and mortality. Clinical, biological, and molecular heterogeneity are well-known hallmarks of cancer and HCC is considered one of the most heterogeneous tumour types, displaying substantial inter-patient, intertumoural and intratumoural variability. This heterogeneity plays a pivotal role in hepatocarcinogenesis, metastasis, relapse and drug response or resistance. Unimodal single-cell sequencing techniques have already revolutionised our understanding of the different layers of molecular hierarchy in the tumour microenvironment of HCC. By highlighting the cellular heterogeneity and the intricate interactions among cancer, immune and stromal cells before and during treatment, these techniques have contributed to a deeper comprehension of tumour clonality, hematogenous spreading and the mechanisms of action of immune checkpoint inhibitors. However, major questions remain to be elucidated, with the identification of biomarkers predicting response or resistance to immunotherapy-based regimens representing an important unmet clinical need. Although the application of single-cell multi-omics in liver cancer research has been limited thus far, a revolution of individualised care for patients with HCC will only be possible by integrating various unimodal methods into multi-omics methodologies at the single-cell resolution. In this review, we will highlight the different established single-cell sequencing techniques and explore their biological and clinical impact on liver cancer research, while casting a glance at the future role of multi-omics in this dynamic and rapidly evolving field.
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  • 文章类型: Journal Article
    作为一种高度侵袭性的肿瘤,原发性肝癌的病理生理机制备受关注。近年来,因素如铁凋亡调节,脂质过氧化和代谢异常已经出现在肝癌的研究中,为了解肝癌的发展提供了新的视角。铁凋亡调节,脂质过氧化和代谢异常在肝癌的发生发展中起重要作用。铁凋亡的调节参与细胞凋亡和坏死,影响细胞存活和死亡。脂质过氧化促进氧化损伤并促进肝癌细胞的侵袭。代谢异常,尤其是糖脂代谢紊乱,直接影响肝癌细胞的增殖和生长。铁凋亡调节和脂质过氧化的研究可能有助于发现新的治疗靶点并改善治疗效果。对代谢异常的认识可以为肝癌的预防提供新思路,并通过调节代谢过程降低患病风险。本文综述了铁凋亡调控的关键作用,脂质过氧化和代谢异常。
    As a highly aggressive tumor, the pathophysiological mechanism of primary liver cancer has attracted much attention. In recent years, factors such as ferroptosis regulation, lipid peroxidation and metabolic abnormalities have emerged in the study of liver cancer, providing a new perspective for understanding the development of liver cancer. Ferroptosis regulation, lipid peroxidation and metabolic abnormalities play important roles in the occurrence and development of liver cancer. The regulation of ferroptosis is involved in apoptosis and necrosis, affecting cell survival and death. Lipid peroxidation promotes oxidative damage and promotes the invasion of liver cancer cells. Metabolic abnormalities, especially the disorders of glucose and lipid metabolism, directly affect the proliferation and growth of liver cancer cells. Studies of ferroptosis regulation and lipid peroxidation may help to discover new therapeutic targets and improve therapeutic outcomes. The understanding of metabolic abnormalities can provide new ideas for the prevention of liver cancer, and reduce the risk of disease by adjusting the metabolic process. This review focuses on the key roles of ferroptosis regulation, lipid peroxidation and metabolic abnormalities in this process.
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  • 文章类型: Journal Article
    晚期肝癌是老年人最常见的恶性肿瘤,但它也发生在乙肝病毒流行地区的年轻人中。本研究的目的是评估全身抗肿瘤治疗对年轻晚期肝癌患者的疗效,并探讨其影响因素。收集38例年轻肝癌患者(≤35岁)的基线人口统计学和临床资料作为A组,79例老年肝癌患者(≥55岁)作为B组,血清谷草转氨酶升高的患者比例无显著组间差异。低血清白蛋白,甲胎蛋白(AFP)和高Child-Pugh评分。A组和B组的中位(m)PFS时间分别为3.9和8.3个月,分别为[危险比(HR),1.702;P=0.009]。A组的mOS(17.6个月)比B组短12.4个月(HR,1.799;P=0.010)。在亚组分析中,男性[HR,1.73;95%置信区间(CI),1.07-2.79],病理诊断(HR,1.79;95%CI,1.10-2.91),以前的手术治疗(HR,2.16;95%CI,1.18-3.95),无肿瘤血栓(HR,2.45;95%CI,1.22-4.93),丙氨酸转氨酶增加(HR,2.23;95%CI,1.07-4.65),天冬氨酸转氨酶增加(HR,3.22;95%CI,1.62-6.39),正常总胆红素(HR,1.77;95%CI,1.09-2.87)和AFP增加(HR,2.02;95%CI,1.19~3.41)与A组生存时间比B组缩短相关(P<0.05)。A组的超进行性疾病(HPD)发生率也较高(31.6vs.3.8%;P<0.001)。HPD是晚期肝癌的危险因素(HR,4.530;95%CI,2.251-9.115;P<0.001]。总之,与老年患者相比,年轻患者的全身抗肿瘤治疗效果较差。年轻肝癌患者HBV感染率高,易发生HPD。
    Advanced liver cancer is the most common malignant tumor in the elderly, but it also occurs in young people in areas where hepatitis B virus is prevalent. The aim of the present study was to assess the efficacy of systemic antitumor therapy in young patients with advanced liver cancer and investigate the influencing factors. The baseline demographic and clinical data of 38 young patients (≤35 years old) with liver cancer were collected as group A and that of 79 elderly patients (≥55 years old) with liver cancer were collected as group B. There were no significant between-group differences regarding the proportion of patients with increased serum aspartate aminotransferase, low serum albumin, increased α-fetoprotein (AFP) and high Child-Pugh score. The median (m)PFS time in groups A and B was 3.9 and 8.3 months, respectively [hazard ratio (HR), 1.702; P=0.009]. The mOS in group A (17.6 months) was 12.4 months shorter than that in group B (HR, 1.799; P=0.010). In the subgroup analysis, male sex [HR, 1.73; 95% confidence interval (CI), 1.07-2.79], pathological diagnosis (HR, 1.79; 95% CI, 1.10-2.91), previous surgical treatment (HR, 2.16; 95% CI, 1.18-3.95), no tumor thrombus (HR, 2.45; 95% CI, 1.22-4.93), increased alanine aminotransferase (HR, 2.23; 95% CI, 1.07-4.65), increased aspartate aminotransferase (HR, 3.22; 95% CI, 1.62-6.39), normal total bilirubin (HR, 1.77; 95% CI, 1.09-2.87) and increased AFP (HR, 2.02; 95% CI, 1.19-3.41) were associated with shorter survival time in group A compared with those in group B (P<0.05). Group A also had a higher incidence of hyper-progressive disease (HPD) (31.6 vs. 3.8%; P<0.001). HPD was a risk factor for advanced liver cancer (HR, 4.530; 95% CI, 2.251-9.115; P<0.001]. In conclusion, the efficacy of systemic antitumor therapy in young patients was poorer compared with that in elderly patients. Young patients with liver cancer had a high HBV infection rate and were prone to HPD.
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