181. High-risk varices in patients with Child-Pugh-Turcotte B and C: consider band ligation with carvedilol for preventing first variceal bleeding, especially in patients with MASLD-associated cirrhosis.183. Metabolic reprogramming by mutant GNAS creates an actionable dependency in intraductal papillary mucinous neoplasms of the pancreas.
作者: Yuki Makino.;Kimal I Rajapakshe.;Benson Chellakkan Selvanesan.;Takashi Okumura.;Kenjiro Date.;Prasanta Dutta.;Lotfi Abou-Elkacem.;Akiko Sagara.;Jimin Min.;Marta Sans.;Nathaniel Yee.;Megan J Siemann.;Jose Enriquez.;Paytience Smith.;Pratip Bhattacharya.;Michael Kim.;Merve Dede.;Traver Hart.;Anirban Maitra.;Fredrik Ivar Thege.
来源: Gut. 2024年74卷1期75-88页
Oncogenic 'hotspot' mutations of KRAS and GNAS are two major driver alterations in intraductal papillary mucinous neoplasms (IPMNs), which are bona fide precursors to pancreatic ductal adenocarcinoma. We previously reported that pancreas-specific KrasG12D and GnasR201C co-expression in p48Cre; KrasLSL-G12D; Rosa26LSL-rtTA; Tg (TetO-GnasR201C) mice ('Kras;Gnas' mice) caused development of cystic lesions recapitulating IPMNs.
184. Targeting TL1A and DR3: the new frontier of anti-cytokine therapy in IBD.
TNF-like cytokine 1A (TL1A) and its functional receptor, death-domain receptor 3 (DR3), are members of the TNF and TNFR superfamilies, respectively, with recognised roles in regulating innate and adaptive immune responses; additional existence of a decoy receptor, DcR3, indicates a tightly regulated cytokine system. The significance of TL1A:DR3 signalling in the pathogenesis of inflammatory bowel disease (IBD) is supported by several converging lines of evidence. Herein, we aim to provide a comprehensive understanding of what is currently known regarding the TL1A/DR3 system in the context of IBD. TL1A and DR3 are expressed by cellular subsets with important roles for the initiation and maintenance of intestinal inflammation, serving as potent universal costimulators of effector immune responses, indicating their participation in the pathogenesis of IBD. Recent evidence also supports a homoeostatic role for TL1A:DR3 via regulation of Tregs and innate lymphoid cells. TL1A and DR3 are also expressed by stromal cells and may contribute to inflammation-induced or inflammation-independent intestinal fibrogenesis. Finally, discovery of genetic polymorphisms with functional consequences may allow for patient stratification, including differential responses to TL1A-targeted therapeutics. In conclusion, TL1A:DR3 signalling plays a central and multifaceted role in the immunological pathways that underlie intestinal inflammation, such as that observed in IBD. Such evidence provides the foundation for developing pharmaceutical approaches targeting this ligand-receptor pair in IBD.
185. Extending inflamed-class signature to predict immune checkpoint inhibitor-based combination therapy in hepatocellular carcinoma.
作者: Wenhua You.;Chupeng Hu.;Mengya Zhao.;Yuhan Zhang.;Jinying Lu.;Yedi Huang.;Ling Li.;Yun Chen.
来源: Gut. 2025年74卷4期679-681页 186. Identification of PRMT5 as a therapeutic target in cholangiocarcinoma.
作者: Jasmin Elurbide.;Leticia Colyn.;Maria U Latasa.;Iker Uriarte.;Stefano Mariani.;Amaya Lopez-Pascual.;Emiliana Valbuena.;Borja Castello-Uribe.;Robert Arnes-Benito.;Elena Adan-Villaescusa.;Luz A Martinez-Perez.;Mikel Azkargorta.;Felix Elortza.;Hanghang Wu.;Marcin Krawczyk.;Kai Markus Schneider.;Bruno Sangro.;Luca Aldrighetti.;Francesca Ratti.;Andrea Casadei Gardini.;Jose J G Marin.;Irene Amat.;Jesus M Urman.;Maria Arechederra.;Maria Luz Martinez-Chantar.;Christian Trautwein.;Meritxell Huch.;Francisco Javier Cubero.;Carmen Berasain.;Maite G Fernandez-Barrena.;Matias A Avila.
来源: Gut. 2024年74卷1期116-127页
Cholangiocarcinoma (CCA) is a very difficult-to-treat cancer. Chemotherapies are little effective and response to immune checkpoint inhibitors is limited. Therefore, new therapeutic strategies need to be identified.
187. Long-term hepatitis B surface antigen response after finite treatment of ARC-520 or JNJ-3989.
作者: Lung Yi Mak.;Christine I Wooddell.;Oliver Lenz.;Thomas Schluep.;James Hamilton.;Heather L Davis.;Xianhua Mao.;Wai-Kay Seto.;Michael Biermer.;Man-Fung Yuen.
来源: Gut. 2025年74卷3期440-450页
RNA interference has been extensively explored in patients with chronic hepatitis B (CHB) infection. We aimed to characterise the long-term efficacy of small interfering RNA (siRNA) on hepatitis B surface antigen (HBsAg) suppression.
188. AlphaMissense versus laboratory-based pathogenicity prediction of 13 novel missense CPA1 variants from pancreatitis cases.
作者: Máté Sándor.;Isabelle Scheers.;Atsushi Masamune.;Heiko Witt.;Jessica LaRusch.;Jian-Min Chen.;Balázs Csaba Németh.;Andrea Geisz.;Aliye Uc.;Miklós Sahin-Tóth.
来源: Gut. 2025年74卷4期678-679页 190. Microbiota-induced S100A11-RAGE axis underlies immune evasion in right-sided colon adenomas and is a therapeutic target to boost anti-PD1 efficacy.
作者: Qiming Zhou.;Linhan Lei.;Junhong Cheng.;Junyou Chen.;Yuyang Du.;Xuehua Zhang.;Qing Li.;Chuangen Li.;Haijun Deng.;Chi Chun Wong.;Baoxiong Zhuang.;Guoxin Li.;Xiaowu Bai.
来源: Gut. 2025年74卷2期214-228页
Tumourigenesis in right-sided and left-sided colons demonstrated distinct features.
191. Sphincterotomy for biliary sphincter of Oddi disorder and idiopathic acute recurrent pancreatitis: the RESPOnD longitudinal cohort.
作者: Gregory A Coté.;Badih Joseph Elmunzer.;Haley Nitchie.;Richard S Kwon.;Field Willingham.;Sachin Wani.;Vladimir Kushnir.;Amitabh Chak.;Vikesh Singh.;Georgios I Papachristou.;Adam Slivka.;Martin Freeman.;Srinivas Gaddam.;Priya Jamidar.;Paul Tarnasky.;Shyam Varadarajulu.;Lydia D Foster.;Peter Cotton.
来源: Gut. 2024年74卷1期58-66页
Sphincter of Oddi disorders (SOD) are contentious conditions in patients whose abdominal pain, idiopathic acute pancreatitis (iAP) might arise from pressurisation at the sphincter of Oddi. The present study aimed to measure the benefit of sphincterotomy for suspected SOD.
192. Risk of hepatic events associated with use of sodium-glucose cotransporter-2 inhibitors versus glucagon-like peptide-1 receptor agonists, and thiazolidinediones among patients with metabolic dysfunction-associated steatotic liver disease.
作者: Sungho Bea.;Hwa Yeon Ko.;Jae Hyun Bae.;Young Min Cho.;Yoosoo Chang.;Seungho Ryu.;Christopher D Byrne.;Ju-Young Shin.
来源: Gut. 2025年74卷2期284-294页
To examine the hepatic effectiveness of sodium-glucose cotransporter-2 inhibitors (SGLT-2i) through a head-to-head comparison with glucagon-like peptide-1 receptor agonists (GLP-1RA) or thiazolidinediones (TZD) in patients with metabolic dysfunction-associated steatotic liver disease (MASLD).
194. Epidemiology of gastrointestinal cancers: a systematic analysis from the Global Burden of Disease Study 2021.
作者: Pojsakorn Danpanichkul.;Kanokphong Suparan.;Primrose Tothanarungroj.;Disatorn Dejvajara.;Krittameth Rakwong.;Yanfang Pang.;Romelia Barba.;Jerapas Thongpiya.;Michael B Fallon.;Denise Harnois.;Rashid N Lui.;Michael B Wallace.;Ju Dong Yang.;Lewis R Roberts.;Karn Wijarnpreecha.
来源: Gut. 2024年74卷1期26-34页
Gastrointestinal cancers comprise nearly one-third of global mortality from cancer, yet the comprehensive global burden of these cancers remains uninvestigated.
196. Where are we with gastric cancer screening in Europe in 2024?
The absolute number of annual cases of gastric cancer in Europe is rising. The Council of the European Union has recommended implementation of gastric cancer screening for countries or regions with a high gastric cancer incidence and death rates. However, as of 2024 no organised gastric cancer screening programme has been launched in Europe.There are several ways to decrease gastric cancer burden, but the screen and treat strategy for Helicobacter pylori (H. pylori) seems to be the most appropriate for Europe. It has to be noted that increased use of antibiotics would be associated with this strategy.Only organised population-based cancer screening is recommended in the European Union, therefore gastric cancer screening also is expected to fulfil the criteria of an organised screening programme. In this respect, several aspects of screening organisation need to be considered before full implementation of gastric cancer prevention in Europe; the age range of the target group, test types, H. pylori eradication regimens and surveillance strategies are among them. Currently, ongoing projects (GISTAR, EUROHELICAN, TOGAS and EUCanScreen) are expected to provide the missing evidence. Feedback from the decision-makers and the potential target groups, including vulnerable populations, will be important to planning the programme.This paper provides an overview of the recent decisions of the European authorities, the progress towards gastric cancer implementation in Europe and expected challenges. Finally, a potential algorithm for gastric cancer screening in Europe is proposed.
197. MED12 loss activates endogenous retroelements to sensitise immunotherapy in pancreatic cancer.
作者: Yingying Tang.;Shijie Tang.;Wenjuan Yang.;Zhengyan Zhang.;Teng Wang.;Yuyun Wu.;Junyi Xu.;Christian Pilarsky.;Massimiliano Mazzone.;Lei-Wei Wang.;Yongwei Sun.;Ruijun Tian.;Yujie Tang.;Yu Wang.;Chaochen Wang.;Jing Xue.
来源: Gut. 2024年73卷12期1999-2011页
Pancreatic ductal adenocarcinoma (PDAC) stands as one of the most lethal cancers, marked by its lethality and limited treatment options, including the utilisation of checkpoint blockade (ICB) immunotherapy. Epigenetic dysregulation is a defining feature of tumourigenesis that is implicated in immune surveillance, but remains elusive in PDAC.
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