1. BVES regulates c-Myc stability via PP2A and suppresses colitis-induced tumourigenesis.
作者: Bobak Parang.;Andrew M Kaz.;Caitlyn W Barrett.;Sarah P Short.;Wei Ning.;Cody E Keating.;Mukul K Mittal.;Rishi D Naik.;Mary K Washington.;Frank L Revetta.;J Joshua Smith.;Xi Chen.;Keith T Wilson.;Thomas Brand.;David M Bader.;William P Tansey.;Ru Chen.;Teresa A Brentnall.;William M Grady.;Christopher S Williams.
来源: Gut. 2017年66卷5期852-862页
Blood vessel epicardial substance (BVES) is a tight junction-associated protein that regulates epithelial-mesenchymal states and is underexpressed in epithelial malignancy. However, the functional impact of BVES loss on tumourigenesis is unknown. Here we define the in vivo role of BVES in colitis-associated cancer (CAC), its cellular function and its relevance to patients with IBD.
4. High impact of methylation accumulation on metachronous gastric cancer: 5-year follow-up of a multicentre prospective cohort study.
作者: Masahiro Maeda.;Takeshi Nakajima.;Ichiro Oda.;Taichi Shimazu.;Nobutake Yamamichi.;Takao Maekita.;Kiyoshi Asada.;Chizu Yokoi.;Takayuki Ando.;Takeichi Yoshida.;Sohachi Nanjo.;Mitsuhiro Fujishiro.;Takuji Gotoda.;Masao Ichinose.;Toshikazu Ushijima.
来源: Gut. 2017年66卷9期1721-1723页 5. TRPM8 polymorphisms associated with increased risk of IBS-C and IBS-M.
作者: Maria Henström.;Fatemeh Hadizadeh.;Arthur Beyder.;Ferdinando Bonfiglio.;Tenghao Zheng.;Ghazaleh Assadi.;Joseph Rafter.;Luis Bujanda.;Lars Agreus.;Anna Andreasson.;Aldona Dlugosz.;Greger Lindberg.;Peter T Schmidt.;Pontus Karling.;Bodil Ohlsson.;Nicholas J Talley.;Magnus Simren.;Susanna Walter.;Mira Wouters.;Gianrico Farrugia.;Mauro D'Amato.
来源: Gut. 2017年66卷9期1725-1727页 6. TSC1/2 mutations define a molecular subset of HCC with aggressive behaviour and treatment implication.
作者: Daniel W H Ho.;Lo K Chan.;Yung T Chiu.;Iris M J Xu.;Ronnie T P Poon.;Tan T Cheung.;Chung N Tang.;Victor W L Tang.;Irene L O Lo.;Polly W Y Lam.;Derek T W Yau.;Miao X Li.;Chun M Wong.;Irene O L Ng.
来源: Gut. 2017年66卷8期1496-1506页
We investigated the mutational landscape of mammalian target of rapamycin (mTOR) signalling cascade in hepatocellular carcinomas (HCCs) with chronic HBV background, aiming to evaluate and delineate mutation-dependent mechanism of mTOR hyperactivation in hepatocarcinogenesis.
7. Efficacy of pancreatic enzyme replacement therapy in chronic pancreatitis: systematic review and meta-analysis.
作者: Daniel de la Iglesia-García.;Wei Huang.;Peter Szatmary.;Iria Baston-Rey.;Jaime Gonzalez-Lopez.;Guillermo Prada-Ramallal.;Rajarshi Mukherjee.;Quentin M Nunes.;J Enrique Domínguez-Muñoz.;Robert Sutton.; .
来源: Gut. 2017年66卷8期1354-1355页
The benefits of pancreatic enzyme replacement therapy (PERT) in chronic pancreatitis (CP) are inadequately defined. We have undertaken a systematic review and meta-analysis of randomised controlled trials of PERT to determine the efficacy of PERT in exocrine pancreatic insufficiency (EPI) from CP.
8. Oncolytic reovirus as a combined antiviral and anti-tumour agent for the treatment of liver cancer.
作者: Adel Samson.;Matthew J Bentham.;Karen Scott.;Gerard Nuovo.;Abigail Bloy.;Elizabeth Appleton.;Robert A Adair.;Rajiv Dave.;Adam Peckham-Cooper.;Giles Toogood.;Seishi Nagamori.;Matthew Coffey.;Richard Vile.;Kevin Harrington.;Peter Selby.;Fiona Errington-Mais.;Alan Melcher.;Stephen Griffin.
来源: Gut. 2018年67卷3期562-573页
Oncolytic viruses (OVs) represent promising, proinflammatory cancer treatments. Here, we explored whether OV-induced innate immune responses could simultaneously inhibit HCV while suppressing hepatocellular carcinoma (HCC). Furthermore, we extended this exemplar to other models of virus-associated cancer.
9. Percutaneous cooled-probe microwave versus radiofrequency ablation in early-stage hepatocellular carcinoma: a phase III randomised controlled trial.
作者: Jie Yu.;Xiao-Ling Yu.;Zhi-Yu Han.;Zhi-Gang Cheng.;Fang-Yi Liu.;Hong-Yan Zhai.;Meng-Juan Mu.;Yan-Mei Liu.;Ping Liang.
来源: Gut. 2017年66卷6期1172-1173页 10. Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome.
作者: Maria Henström.;Lena Diekmann.;Ferdinando Bonfiglio.;Fatemeh Hadizadeh.;Eva-Maria Kuech.;Maren von Köckritz-Blickwede.;Louise B Thingholm.;Tenghao Zheng.;Ghazaleh Assadi.;Claudia Dierks.;Martin Heine.;Ute Philipp.;Ottmar Distl.;Mary E Money.;Meriem Belheouane.;Femke-Anouska Heinsen.;Joseph Rafter.;Gerardo Nardone.;Rosario Cuomo.;Paolo Usai-Satta.;Francesca Galeazzi.;Matteo Neri.;Susanna Walter.;Magnus Simrén.;Pontus Karling.;Bodil Ohlsson.;Peter T Schmidt.;Greger Lindberg.;Aldona Dlugosz.;Lars Agreus.;Anna Andreasson.;Emeran Mayer.;John F Baines.;Lars Engstrand.;Piero Portincasa.;Massimo Bellini.;Vincenzo Stanghellini.;Giovanni Barbara.;Lin Chang.;Michael Camilleri.;Andre Franke.;Hassan Y Naim.;Mauro D'Amato.
来源: Gut. 2018年67卷2期263-270页
IBS is a common gut disorder of uncertain pathogenesis. Among other factors, genetics and certain foods are proposed to contribute. Congenital sucrase-isomaltase deficiency (CSID) is a rare genetic form of disaccharide malabsorption characterised by diarrhoea, abdominal pain and bloating, which are features common to IBS. We tested sucrase-isomaltase (SI) gene variants for their potential relevance in IBS.
11. Modifiable lifestyle factors associated with risk of sessile serrated polyps, conventional adenomas and hyperplastic polyps.
作者: James R Davenport.;Timothy Su.;Zhiguo Zhao.;Helen G Coleman.;Walter E Smalley.;Reid M Ness.;Wei Zheng.;Martha J Shrubsole.
来源: Gut. 2018年67卷3期456-465页
To identify modifiable factors associated with sessile serrated polyps (SSPs) and compare the association of these factors with conventional adenomas (ADs) and hyperplastic polyps (HPs).
12. Palbociclib (PD-0332991), a selective CDK4/6 inhibitor, restricts tumour growth in preclinical models of hepatocellular carcinoma.
作者: Julien Bollard.;Verónica Miguela.;Marina Ruiz de Galarreta.;Anu Venkatesh.;C Billie Bian.;Mark P Roberto.;Victoria Tovar.;Daniela Sia.;Pedro Molina-Sánchez.;Christie B Nguyen.;Shigeki Nakagawa.;Josep M Llovet.;Yujin Hoshida.;Amaia Lujambio.
来源: Gut. 2017年66卷7期1286-1296页
Advanced hepatocellular carcinoma (HCC) is a lethal malignancy with limited treatment options. Palbociclib, a well-tolerated and selective CDK4/6 inhibitor, has shown promising results in the treatment of retinoblastoma (RB1)-positive breast cancer. RB1 is rarely mutated in HCC, suggesting that palbociclib could potentially be used for HCC therapy. Here, we provide a comprehensive characterisation of the efficacy of palbociclib in multiple preclinical models of HCC.
13. Protein and glycomic plasma markers for early detection of adenoma and colon cancer.
作者: Jung-Hyun Rho.;Jon J Ladd.;Christopher I Li.;John D Potter.;Yuzheng Zhang.;David Shelley.;David Shibata.;Domenico Coppola.;Hiroyuki Yamada.;Hidenori Toyoda.;Toshifumi Tada.;Takashi Kumada.;Dean E Brenner.;Samir M Hanash.;Paul D Lampe.
来源: Gut. 2018年67卷3期473-484页
To discover and confirm blood-based colon cancer early-detection markers.
14. Epigenetic treatment of pancreatic cancer: is there a therapeutic perspective on the horizon?
作者: Elisabeth Hessmann.;Steven A Johnsen.;Jens T Siveke.;Volker Ellenrieder.
来源: Gut. 2017年66卷1期168-179页
Pancreatic ductal adenocarcinoma (PDAC) constitutes one of the most aggressive malignancies with a 5-year survival rate of <7%. Due to growing incidence, late diagnosis and insufficient treatment options, PDAC is predicted to soon become one of the leading causes of cancer-related death. Although intensified cytostatic combinations, particularly gemcitabine plus nab-paclitaxel and the folinic acid, fluorouracil, irinotecan, oxaliplatin (FOLFIRINOX) protocol, provide some improvement in efficacy and survival compared with gemcitabine alone, a breakthrough in the treatment of metastatic pancreatic cancer remains out of sight. Nevertheless, recent translational research activities propose that either modulation of the immune response or pharmacological targeting of epigenetic modifications alone, or in combination with chemotherapy, might open highly powerful therapeutic avenues in GI cancer entities, including pancreatic cancer. Deregulation of key epigenetic factors and chromatin-modifying proteins, particularly those responsible for the addition, removal or recognition of post-translational histone modifications, are frequently found in human pancreatic cancer and hence constitute particularly exciting treatment opportunities. This review summarises both current clinical trial activities and discovery programmes initiated throughout the biopharma landscape, and critically discusses the chances, hurdles and limitations of epigenetic-based therapy in future PDAC treatment.
15. Alterations in the epithelial stem cell compartment could contribute to permanent changes in the mucosa of patients with ulcerative colitis.
作者: Isabella Dotti.;Rut Mora-Buch.;Elena Ferrer-Picón.;Núria Planell.;Peter Jung.;M Carme Masamunt.;Raquel Franco Leal.;Javier Martín de Carpi.;Josep Llach.;Ingrid Ordás.;Eduard Batlle.;Julián Panés.;Azucena Salas.
来源: Gut. 2017年66卷12期2069-2079页
UC is a chronic inflammatory disease of the colonic mucosa. Growing evidence supports a role for epithelial cell defects in driving pathology. Moreover, long-lasting changes in the epithelial barrier have been reported in quiescent UC. Our aim was to investigate whether epithelial cell defects could originate from changes in the epithelial compartment imprinted by the disease.
18. Interplay of host genetics and gut microbiota underlying the onset and clinical presentation of inflammatory bowel disease.
作者: Floris Imhann.;Arnau Vich Vila.;Marc Jan Bonder.;Jingyuan Fu.;Dirk Gevers.;Marijn C Visschedijk.;Lieke M Spekhorst.;Rudi Alberts.;Lude Franke.;Hendrik M van Dullemen.;Rinze W F Ter Steege.;Curtis Huttenhower.;Gerard Dijkstra.;Ramnik J Xavier.;Eleonora A M Festen.;Cisca Wijmenga.;Alexandra Zhernakova.;Rinse K Weersma.
来源: Gut. 2018年67卷1期108-119页
Patients with IBD display substantial heterogeneity in clinical characteristics. We hypothesise that individual differences in the complex interaction of the host genome and the gut microbiota can explain the onset and the heterogeneous presentation of IBD. Therefore, we performed a case-control analysis of the gut microbiota, the host genome and the clinical phenotypes of IBD.
19. Expert opinions and scientific evidence for colonoscopy key performance indicators.
作者: Colin J Rees.;Roisin Bevan.;Katharina Zimmermann-Fraedrich.;Matthew D Rutter.;Douglas Rex.;Evelien Dekker.;Thierry Ponchon.;Michael Bretthauer.;Jaroslaw Regula.;Brian Saunders.;Cesare Hassan.;Michael J Bourke.;Thomas Rösch.
来源: Gut. 2016年65卷12期2045-2060页
Colonoscopy is a widely performed procedure with procedural volumes increasing annually throughout the world. Many procedures are now performed as part of colorectal cancer screening programmes. Colonoscopy should be of high quality and measures of this quality should be evidence based. New UK key performance indicators and quality assurance standards have been developed by a working group with consensus agreement on each standard reached. This paper reviews the scientific basis for each of the quality measures published in the UK standards.
20. Molecular classification of Crohn's disease reveals two clinically relevant subtypes.
作者: Matthew Weiser.;Jeremy M Simon.;Bharati Kochar.;Adelaide Tovar.;Jennifer W Israel.;Adam Robinson.;Gregory R Gipson.;Matthew S Schaner.;Hans H Herfarth.;R Balfour Sartor.;Dermot P B McGovern.;Reza Rahbar.;Timothy S Sadiq.;Mark J Koruda.;Terrence S Furey.;Shehzad Z Sheikh.
来源: Gut. 2018年67卷1期36-42页
The clinical presentation and course of Crohn's disease (CD) is highly variable. We sought to better understand the cellular and molecular mechanisms that guide this heterogeneity, and characterise the cellular processes associated with disease phenotypes.
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