Role of Aquaporin-5 in Gallbladder Carcinoma

2013 ◽  
Vol 51 (3-4) ◽  
pp. 108-117 ◽  
Author(s):  
S. Sekine ◽  
Y. Shimada ◽  
T. Nagata ◽  
S. Sawada ◽  
I. Yoshioka ◽  
...  
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Davide Di Mauro ◽  
Amira Orabi ◽  
Aye Myintmo ◽  
Alex Reece-Smith ◽  
Shahjehan Wajed ◽  
...  

Abstract Background Gallbladder carcinoma is often found incidentally on histopathologic examination after cholecystectomy—this is referred as incidental gallbladder carcinoma (IGC). Routine vs selective histopathological assessment of gallbladders is under debate and this study evaluates the role of regular specimens’ examination, based on a single-centre analysis of incidence, clinical and histopathological aspects of IGC. Methods Patients who underwent cholecystectomy, between July 2010 and January 2020, were considered. Exclusion criteria were age under 18 and preoperative diagnosis of GB carcinoma. Demographic, clinical and histopathological data were retrospectively collected, continuous variables with a normal distribution were evaluated with Student’s t-test and ANOVA. Results Some 5779 patients were included. The female/male ratio was 2.5:1. Chronic cholecystitis (CC) was the most common finding on specimens (99.3%), IGC was found in six cases (0.1%). In the latter group, there were 5 women and patients were older than those with benign disease—73.7 $$\pm$$ ±  5.38 years vs 55.8 $$\pm$$ ±  0.79 years (p < 0.05). In all the cases, the GB was abnormal on intraoperative inspection and beside cancer, histopathology showed associated CC and/or dysplasia. Upon diagnosis, disease was at advanced stage—one stage II, one stage IIIA, one stage IIIB, three stage IVA. Two patients are alive, three died of disease progression—median survival was 7 months (range 2–14). Conclusions In this series, ICG was rare, occurred most commonly in old adult women and was diagnosed at an advanced stage. In all the cases, the GB was abnormal intraoperatively, therefore macroscopic GB anomalies demand histopathological assessment of the specimen.


2007 ◽  
Vol 353 (4) ◽  
pp. 1017-1022 ◽  
Author(s):  
Johji Nomura ◽  
Akinori Hisatsune ◽  
Takeshi Miyata ◽  
Yoichiro Isohama

2018 ◽  
Vol 12 (10) ◽  
pp. 1095-1103 ◽  
Author(s):  
Xi-Fen Liu ◽  
Lin-Ying Zhou ◽  
Zi-Hao Wei ◽  
Jia-Xin Liu ◽  
Ang Li ◽  
...  

Author(s):  
Helene H. Jensen ◽  
Frédéric H. Login ◽  
Jennifer S. Koffman ◽  
Tae-Hwan Kwon ◽  
Lene N. Nejsum

Cells ◽  
2020 ◽  
Vol 9 (4) ◽  
pp. 904
Author(s):  
Lars Bergmann ◽  
Hartmuth Nowak ◽  
Winfried Siffert ◽  
Jürgen Peters ◽  
Michael Adamzik ◽  
...  

Since the functionally important AQP5 -1364A/C single nucleotide promoter polymorphism alters key mechanisms of inflammation and survival in sepsis, it may affect the risk of an acute kidney injury. Accordingly, we tested the hypothesis in septic patients that this AQP5 polymorphism is associated with major adverse kidney events and also validated its impact on 90-day survival. In this prospective observational monocentric genetic association study 282 septic patients were included and genotyped for the AQP5 –1364A/C polymorphism (rs3759129). The primary endpoint was the development of major adverse kidney events within 30 days. In AC/CC genotypes, major adverse kidney events were less frequent (41.7%) than in AA genotypes (74.3%; OR:0.34; 95%-CI: 0.18–0.62; p < 0.001). Ninety-day survival was also associated with the AQP5 polymorphism (p = 0.004), with 94/167 deaths (56.3%) in AA genotypes, but only 46/115 deaths (40.0%) in C-allele carriers. Multiple proportional hazard analysis revealed AC/CC genotypes to be at significantly lower risk for death within 90 days (HR: 0.60; 95%-CI: 0.42-0.86; p = 0.006). These findings confirm the important role of the AQP5 -1364A/C polymorphism as an independent prognostic factor in sepsis. Furthermore, we demonstrate a strong association between this AQP5 polymorphism and susceptibility for major adverse kidney events suggesting a promising characteristic in terms of precision medicine.


1989 ◽  
Vol 76 (5) ◽  
pp. 448-450 ◽  
Author(s):  
S. Houry ◽  
M. Schlienger ◽  
M. Huguier ◽  
F. Lacaine ◽  
F. Penne ◽  
...  

2012 ◽  
Vol 13 (10) ◽  
pp. 536-540 ◽  
Author(s):  
Somprakas Basu ◽  
Rupesh Priya ◽  
Tej Bali Singh ◽  
Pradeep Srivastava ◽  
Pradeep K. Mishra ◽  
...  

2008 ◽  
Vol 173 (2) ◽  
pp. 518-525 ◽  
Author(s):  
Sung Koo Kang ◽  
Young Kwang Chae ◽  
Janghee Woo ◽  
Myoung Sook Kim ◽  
Jong Chul Park ◽  
...  

Tumor Biology ◽  
2014 ◽  
Vol 35 (7) ◽  
pp. 6191-6192 ◽  
Author(s):  
Ji-Liang Xu ◽  
Rong Xia
Keyword(s):  

2010 ◽  
Vol 138 (5) ◽  
pp. S-867
Author(s):  
Kazuaki Shimada ◽  
Daisuke Ban ◽  
Yusuke Yamamoto ◽  
Satoshi Nara ◽  
Minoru Esaki ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document