4122. γδ Intraepithelial Lymphocytes Facilitate Pathological Epithelial Cell Shedding Via CD103-Mediated Granzyme Release.
作者: Madeleine D Hu.;Natasha B Golovchenko.;Grace L Burns.;Prema M Nair.;Thomas J Kelly.;Jonathan Agos.;Mudar Zand Irani.;Wai Sinn Soh.;Matthew R Zeglinski.;Alexander Lemenze.;Edward M Bonder.;Inga Sandrock.;Immo Prinz.;David J Granville.;Simon Keely.;Alastair J M Watson.;Karen L Edelblum.
来源: Gastroenterology. 2022年162卷3期877-889.e7页
Excessive shedding of apoptotic enterocytes into the intestinal lumen is observed in inflammatory bowel disease and is correlated with disease relapse. Based on their cytolytic capacity and surveillance behavior, we investigated whether intraepithelial lymphocytes expressing the γδ T cell receptor (γδ IELs) are actively involved in the shedding of enterocytes into the lumen.
4127. Dissection of Barrier Dysfunction in Organoid-Derived Human Intestinal Epithelia Induced by Giardia duodenalis.
作者: David Holthaus.;Martin R Kraft.;Susanne M Krug.;Silver Wolf.;Antonia Müller.;Estefania Delgado Betancourt.;Madeleine Schorr.;Gudrun Holland.;Felix Knauf.;Joerg-Dieter Schulzke.;Toni Aebischer.;Christian Klotz.
来源: Gastroenterology. 2022年162卷3期844-858页
The protozoa Giardia duodenalis is a major cause of gastrointestinal illness worldwide, but underlying pathophysiological mechanisms remain obscure, partly due to the absence of adequate cellular models. We aimed at overcoming these limitations and recapitulating the authentic series of pathogenic events in the primary human duodenal tissue by using the human organoid system.
4129. Late-Stage Pancreatic Cancer Detected During High-Risk Individual Surveillance: A Systematic Review and Meta-Analysis.
作者: Ankit Chhoda.;Ziga Vodusek.;Kapil Wattamwar.;Eric Mukherjee.;Craig Gunderson.;Alyssa Grimshaw.;Anup Sharma.;Nita Ahuja.;Fay Kastrinos.;James J Farrell.
来源: Gastroenterology. 2022年162卷3期786-798页
Identification and resection of successful targets, that is, T1 N0M0 pancreatic ductal adenocarcinoma (PDAC) and high-grade precursors during surveillance of high-risk individuals (HRIs) confers improved survival. Late-stage PDACs refer to T2-4 N0M0 and nodal or distant metastatic PDAC stages diagnosed during the follow-up phase of HRI surveillance. This study aimed to quantify late-stage PDACs during HRI surveillance and identify associated clinicoradiologic factors.
4131. Impact of Coronavirus Disease 2019 on the Diagnosis and Therapy for Barrett's Esophagus and Esophageal Cancer in the United States.
作者: Arvind J Trindade.;Jianying Zhang.;John Hauschild.;Cadman L Leggett.;Prasad G Iyer.
来源: Gastroenterology. 2022年162卷3期978-980.e6页 4135. Updates on Age to Start and Stop Colorectal Cancer Screening: Recommendations From the U.S. Multi-Society Task Force on Colorectal Cancer.
作者: Swati G Patel.;Folasade P May.;Joseph C Anderson.;Carol A Burke.;Jason A Dominitz.;Seth A Gross.;Brian C Jacobson.;Aasma Shaukat.;Douglas J Robertson.
来源: Gastroenterology. 2022年162卷1期285-299页
This document is a focused update to the 2017 colorectal cancer (CRC) screening recommendations from the U.S. Multi-Society Task Force on Colorectal Cancer, which represents the American College of Gastroenterology, the American Gastroenterological Association, and the American Society for Gastrointestinal Endoscopy. This update is restricted to addressing the age to start and stop CRC screening in average-risk individuals and the recommended screening modalities. Although there is no literature demonstrating that CRC screening in individuals under age 50 improves health outcomes such as CRC incidence or CRC-related mortality, sufficient data support the U.S. Multi-Society Task Force to suggest average-risk CRC screening begin at age 45. This recommendation is based on the increasing disease burden among individuals under age 50, emerging data that the prevalence of advanced colorectal neoplasia in individuals ages 45 to 49 approaches rates in individuals 50 to 59, and modeling studies that demonstrate the benefits of screening outweigh the potential harms and costs. For individuals ages 76 to 85, the decision to start or continue screening should be individualized and based on prior screening history, life expectancy, CRC risk, and personal preference. Screening is not recommended after age 85.
4139. Exploration of inflammation, oxidative stress, adiponectin and intestinal flora in patients with hepatitis B, liver cirrhosis and hepatocellular carcinoma.
作者: Jing Xu.;Kun Liu.;Zhufang Ma.;Yongmei Lin.;Linyuan Pang.
来源: Minerva Gastroenterol (Torino). 2022年68卷3期365-367页 4140. MiR-34a targets SNAI1 and is essential for 5-hydroxytryptamine induced epithelial mesenchymal transition in liver cancer.
作者: Zhixin Wang.;Wen Wang.;Liuxin Zhou.;Li Ren.;Runchen Miao.;Kai Qu.;Bin Ren.;Wenhao Yu.;Haijiu Wang.;Chang Liu.;Haining Fan.
来源: Minerva Gastroenterol (Torino). 2022年68卷3期363-365页 |