iLIVERPub Date : 2024-11-09DOI: 10.1016/j.iliver.2024.100129
Alfred Wei-Chieh Kow
{"title":"Speaking the same language in predicting Small-for-Size Syndrome in living donor liver transplantation","authors":"Alfred Wei-Chieh Kow","doi":"10.1016/j.iliver.2024.100129","DOIUrl":"10.1016/j.iliver.2024.100129","url":null,"abstract":"","PeriodicalId":100657,"journal":{"name":"iLIVER","volume":"3 4","pages":"Article 100129"},"PeriodicalIF":0.0,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142707081","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
iLIVERPub Date : 2024-11-07DOI: 10.1016/j.iliver.2024.100132
Ling Chu , Junbo Zhang , Ruoyu Meng , Quan Zhuang
{"title":"Evaluating the role of IER3+ macrophages in the prognosis of liver fibrosis by bulk and single-cell transcriptional analyses","authors":"Ling Chu , Junbo Zhang , Ruoyu Meng , Quan Zhuang","doi":"10.1016/j.iliver.2024.100132","DOIUrl":"10.1016/j.iliver.2024.100132","url":null,"abstract":"<div><h3>Background and aims</h3><div>Liver fibrosis (LF) is the common pathological process of almost all liver diseases, but the pathogenesis is extremely complicated and has not been fully clarified. Therefore, we want to explore LF's complex pathogenesis and identify key genetic markers that can predict LF prognosis.</div></div><div><h3>Methods</h3><div>From Gene Expression Omnibus (GEO, <span><span>https://www.ncbi.nlm.nih.gov/geo/</span><svg><path></path></svg></span>), we contained datasets GSE84044 and GSE130970. And involved GSE15654 whose survival data were for the validation of our model’s prognostic value. Then, Bulk RNA sequencing was used to establish a LF-related prognostic model and to determine key genes.The key genes were later analyzed using single-cell RNA sequencing (scRNA-seq) and the role of macrophages in LF was investigated.</div></div><div><h3>Results</h3><div>We established a comprehensive LF-related prognostic model (FMSig, i.e., fibrosis macrophage-related prognostic signature) containing four genes (IER3, AKR1B10, ADCY1, and PGM1). FMSig can distinguish between survival outcomes in dataset GSE15654. IER3 showed a higher hazard ratio than the other three FMSig genes. Moreover, further scRNA-seq analysis showed that IER3 is highly expressed in myeloid cells while the other three genes were rarely expressed in six immune cell types and other cell clusters. After reclustering the myeloid cells into seven clusters, we found that IER3 was highly expressed in myeloid cell cluster 3, shown to be related to anti-inflammation and lipid metabolism functions. Based on pseudotime analysis, we suggest that myeloid cell type 3 is transformed from myeloid cell type 0 in the liver cirrhosis microenvironment. On immunohistochemical staining, LF showed significantly higher IER3 expression than healthy controls.</div></div><div><h3>Conclusion</h3><div>This study established a predictive model, FMSig, to evaluate LF prognosis, and showed that IER3 and macrophages are related to LF.</div></div>","PeriodicalId":100657,"journal":{"name":"iLIVER","volume":"3 4","pages":"Article 100132"},"PeriodicalIF":0.0,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142706992","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
iLIVERPub Date : 2024-11-07DOI: 10.1016/j.iliver.2024.100130
Binghua Li , Qiang Wang , Weiwei Hu , Huan Li , Peng Yan , Yajuan Cao , Decai Yu
{"title":"Comment on “Clinical outcomes and histologic findings of patients with hepatocellular carcinoma with durable partial response or durable stable disease after receiving atezolizumab plus bevacizumab”","authors":"Binghua Li , Qiang Wang , Weiwei Hu , Huan Li , Peng Yan , Yajuan Cao , Decai Yu","doi":"10.1016/j.iliver.2024.100130","DOIUrl":"10.1016/j.iliver.2024.100130","url":null,"abstract":"","PeriodicalId":100657,"journal":{"name":"iLIVER","volume":"3 4","pages":"Article 100130"},"PeriodicalIF":0.0,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142719874","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
iLIVERPub Date : 2024-11-06DOI: 10.1016/j.iliver.2024.100127
Tian Yang , Ming-Da Wang , Gui-Lin Xie , Xiong-Hua Wang , Liu Zheng , Li-Min Wang , Guang-Fa Xiao , Yong-Qing Yang , Chao Li , Alfred Wei Chieh Kow , Feng Shen
{"title":"Danning tablets for the treatment of multiple gallbladder polyps: Study protocol of multicentre, randomised, open-labelled, controlled trial","authors":"Tian Yang , Ming-Da Wang , Gui-Lin Xie , Xiong-Hua Wang , Liu Zheng , Li-Min Wang , Guang-Fa Xiao , Yong-Qing Yang , Chao Li , Alfred Wei Chieh Kow , Feng Shen","doi":"10.1016/j.iliver.2024.100127","DOIUrl":"10.1016/j.iliver.2024.100127","url":null,"abstract":"<div><h3>Introduction</h3><div>Gallbladder polyps (GPs) are protrusions of the gallbladder wall into the lumen, and are commonly detected during ultrasound examinations. Traditional management of multiple GPs (MGPs) has been conservative, including lifestyle interventions, regular monitoring, and surgical intervention in certain cases, but this approach poses risks of polyps enlargement and increase of number, as well as patients’ psychological burdens. Danning Tablets, a traditional Chinese medicine, have emerged as a potential non-surgical treatment for GPs, showing promise in reducing polyp size and alleviating symptoms, backed by their anti-inflammatory and antitumor properties demonstrated in preclinical studies. This suggests the need for further research into Danning Tablets as an alternative treatment for MGPs.</div></div><div><h3>Methods and analysis</h3><div>The study is designed as a prospective, randomized, controlled, open-label trial. The study will be conducted across multiple centres specializing in gastroenterology and hepatology. Participants will be recruited from these centres, ensuring a diverse patient demographic. Adult patients diagnosed with MGPs, based on ultrasound findings, will be included. Exclusion criteria include patients with a history of gallbladder cancer, previous gallbladder surgery, or serious comorbid conditions. The control group will receive standard care, including dietary and lifestyle advice, while the intervention group will receive Danning Tablets and standard care. The dosage and administration of Danning Tablets will follow established clinical guidelines. The primary outcome will be the change in size of the largest gallbladder polyps on week 24 ± 1, measured by ultrasound. The secondary outcomes will include symptom improvement and recording of any adverse events. The study will span over a period of 6 months, with periodic assessments at baseline, 4, 8, 12, and 24 weeks.</div></div>","PeriodicalId":100657,"journal":{"name":"iLIVER","volume":"3 4","pages":"Article 100127"},"PeriodicalIF":0.0,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142706991","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
iLIVERPub Date : 2024-11-06DOI: 10.1016/j.iliver.2024.100126
Yu-Ting Xiong, Chun-Yan Wang, Dong Ji
{"title":"Reply to Dr. Sun et al.: Female DILI patients need more clinical attention","authors":"Yu-Ting Xiong, Chun-Yan Wang, Dong Ji","doi":"10.1016/j.iliver.2024.100126","DOIUrl":"10.1016/j.iliver.2024.100126","url":null,"abstract":"","PeriodicalId":100657,"journal":{"name":"iLIVER","volume":"3 4","pages":"Article 100126"},"PeriodicalIF":0.0,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142706993","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
iLIVERPub Date : 2024-10-30DOI: 10.1016/j.iliver.2024.100125
Xiaoru Sun , Xinrong Zhang , Muyun Liu
{"title":"Increased attention to women with drug-induced liver injury: Risk factors and early intervention","authors":"Xiaoru Sun , Xinrong Zhang , Muyun Liu","doi":"10.1016/j.iliver.2024.100125","DOIUrl":"10.1016/j.iliver.2024.100125","url":null,"abstract":"<div><div>A recent study by Xiong Yu-Ting and colleagues has unveiled the clinical characteristics and risk factors of acute drug-induced liver injury (DILI). Upon reading the article, we found that there are some differences between female and male patients with DILI in terms of clinical and pathological features, especially in the number of patients, the degree of liver inflammation, and the risk of autoimmune liver disease. Therefore, it is necessary to pay attention to female patients with DILI and their outcomes, and to intervene appropriately in advance. This article analyzes the reasons for the differences between female and male patients with DILI and makes recommendations for patient prognosis.</div></div>","PeriodicalId":100657,"journal":{"name":"iLIVER","volume":"3 4","pages":"Article 100125"},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142651488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Arginine methylation modification in the malignant progression of benign and malignant liver diseases","authors":"Jie-Zuo Huang , Bei-Ning Qiao , Dang-Chi Li , Qiu-Rong Wei , Zi-Jian Zhang","doi":"10.1016/j.iliver.2024.100124","DOIUrl":"10.1016/j.iliver.2024.100124","url":null,"abstract":"<div><div>The role of protein arginine methyltransferases (PRMTs) in benign and malignant liver diseases has garnered considerable attention. PRMTs play a key function in regulating protein methylation modification in diseases such as alcoholic fatty liver disease, metabolic dysfunction–associated steatotic liver disease, viral hepatitis, and hepatocellular carcinoma. This review explores the mechanisms of action of PRMTs in these diseases, with a focus on their effects on cell signaling, transcriptional regulation, cell proliferation, and metabolism. We also discuss potential therapeutic strategies targeting PRMTs and propose future research directions. This review helps deepen the understanding of the important role of arginine methylation modification in the malignant progression of liver diseases and provides guidance for future clinical treatment and drug development.</div></div>","PeriodicalId":100657,"journal":{"name":"iLIVER","volume":"3 4","pages":"Article 100124"},"PeriodicalIF":0.0,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142528996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
iLIVERPub Date : 2024-09-18DOI: 10.1016/j.iliver.2024.100117
Zhiwei Ye , Jing Zhao , Dandan Hu , Zhoutian Yang , Jinbin Chen , Li Xu , Zhongguo Zhou , Minshan Chen , Yaojun Zhang
{"title":"Gd-EOB-DTPA-enhanced MRI proves advantageous in selecting surgical candidates for patients with early-stage hepatocellular carcinoma: An analysis in terms of oncological outcomes","authors":"Zhiwei Ye , Jing Zhao , Dandan Hu , Zhoutian Yang , Jinbin Chen , Li Xu , Zhongguo Zhou , Minshan Chen , Yaojun Zhang","doi":"10.1016/j.iliver.2024.100117","DOIUrl":"10.1016/j.iliver.2024.100117","url":null,"abstract":"<div><h3>Background and aims</h3><div>To determine the value of preoperative Gd-EOB-DTPA-enhanced magnetic resonance imaging (MRI) in comparison with extracellular contrast agent MRI and CT in the selection of surgical candidates among patients with hepatocellular carcinoma (HCC), particularly in terms of oncological outcomes after hepatectomy.</div></div><div><h3>Methods</h3><div>This retrospective study included 542 consecutive patients who underwent radical hepatectomy for HCC. One group underwent preoperative Gd-EOB-DTPA-enhanced MRI, one group underwent contrast-enhanced CT, and one group underwent extracellular contrast agent MRI. We compared oncologic outcomes including recurrence free survival and overall survival between the three groups. Subgroup analyses were also performed to provide more specific candidates or beneficiaries for preoperative EOB-MRI.</div></div><div><h3>Results</h3><div>A total of 244 patients had tumor recurrence, with 55 in the EOB-MRI group, 106 in the Routine-MRI group, and 83 in the CT group (<em>p</em> = 0.010). The numbers with early recurrence (<2 years) in each group were 40 (27.03%), 78 (35.78%), and 62 (35.22%), respectively (<em>p</em> = 0.018). The 1, 2, and 3-year recurrence-free survival (RFS) percentages were 82.4%, 73.0%, and 68.2% in the EOB-MRI group, 70.2%, 64.3%, and 56.9% in the Routine-MRI group, and 76.8%, 64.83%, and 58.9% in the CT group (<em>p</em> = 0.010). The 1, 2, and 3-year overall survival percentages were 89.19%, 83.11%, and 80.41% in the EOB-MRI group, 79.82%, 73.86%, and 67.44% in the Routine-MRI group, and 86.55%, 76.14%, and 69.32% in the CT group (<em>p</em> = 0.016). Subgroup analysis showed significant differences in RFS in patients with solitary tumor <3 cm.</div></div><div><h3>Conclusion</h3><div>Preoperative EOB-MRI is superior to contrast-enhanced CT or extracellular contrast agent MRI for selecting surgical candidates at low risk of recurrence following hepatic resection for HCC.</div></div>","PeriodicalId":100657,"journal":{"name":"iLIVER","volume":"3 4","pages":"Article 100117"},"PeriodicalIF":0.0,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142434033","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
iLIVERPub Date : 2024-09-01DOI: 10.1016/j.iliver.2024.100115
Wenze Wu , Yuzhu Shi , Yongzi Wu , Rui Zhang , Xinyan Wu , Weidi Zhao , Zhiyuan Chen , Gang Ye
{"title":"Network pharmacology and single-cell transcriptomic analysis with molecular docking to elucidate the potential compounds and targets of Polygonum cuspidatum Sieb.et Zucc. for hepatocellular carcinoma","authors":"Wenze Wu , Yuzhu Shi , Yongzi Wu , Rui Zhang , Xinyan Wu , Weidi Zhao , Zhiyuan Chen , Gang Ye","doi":"10.1016/j.iliver.2024.100115","DOIUrl":"10.1016/j.iliver.2024.100115","url":null,"abstract":"<div><h3>Background and aims</h3><p><em>Polygonum cuspidatum</em> Sieb.et Zucc. (<em>P. cuspidatum</em>) and its active components have been clinically proven to have anti-hepatocellular carcinoma effects. However, the potential targets of <em>P. cuspidatum</em> for these effects have not yet been revealed.</p></div><div><h3>Methods</h3><p>We used network pharmacology and single-cell transcriptomic analysis with molecular docking to elucidate the active components and targets of <em>P. cuspidatum</em> for hepatocellular carcinoma.</p></div><div><h3>Results</h3><p>CDK1, ESR1, HSP90A11, and MAPK1 were shown to be the key targets of <em>P. cuspidatum</em> for hepatocellular carcinoma. <em>P. cuspidatum</em> was found to be likely correlated with the improved abnormal expression of CDK1 and ESR1 and the poor prognosis of HSP90AA1 and MAPK1. CDK1 was identified as the most potential anti-hepatocellular carcinoma target of <em>P. cuspidatum</em>. Among the active components of <em>P. cuspidatum</em>, physcion diglucoside was found to have the most potential to treat hepatocellular carcinoma by targeting CDK1.</p></div><div><h3>Conclusion</h3><p>Our study provides novel insights into the anti-hepatocellular carcinoma pharmacological effects of <em>P. cuspidatum</em>, which could serve as a scientific basis for its development as a medicinal resource and the targeting of CDK1 for hepatocellular carcinoma treatment.</p></div>","PeriodicalId":100657,"journal":{"name":"iLIVER","volume":"3 3","pages":"Article 100115"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772947824000409/pdfft?md5=11fd39f142c9e35b0e9dd563005a3e5a&pid=1-s2.0-S2772947824000409-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142172692","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}