Scientific Program

Conference Series Ltd invites all the participants across the globe to attend 6th International Conference on Hepatology Osaka, Japan.

Day :

  • Liver and Biliary
Location: Hyatt Regency Osaka

Session Introduction

Omer Engin

Associate Professor of General Surgery. Health Sciences University, Tepecik Training and Research Hospital, Surgery Department, Izmir, Turkey

Title: Management of liver trauma: Case reports and literature review
Biography:

Omer Engin MD,

Associate Professor of General Surgery. Health Sciences University, Tepecik Training and Research Hospital, Surgery Department, Izmir, Turkey

Abstract:

A lot of surgeons may not do liver resection for malignancy in their surgical practice but they may have to operate liver because of traumatic injuries of liver. Such operations can be changed from simple suturing to resection. So, all of the surgeons must know liver anatomy and surgical operation techniques.

Liver injuries may occur after blunt or penetrating injuries. Clinical presentation may change from silent symptoms to shock symptoms. There are two liver injuries cases are presented except for another all of our liver injuries cases.

Some imaging modalities can be used that ultrasonography, CT, MRI as a noninvasive. Diagnostic peritoneal lavage and laparoscopy can be chosen such as invasive techniques.

Treatment of this lacerations can be divided into medical and surgical. Parenteral replacement of liquid, erythrocyte, thrombocyte and fresh frozen plasma are in the medical treatment options of the liver lacerations. Surgical management of the liver varies from patient to patient.

Biography:

Jordan University of Science and Technology, Jordan

Abstract:

Introduction & Aim: Fungal organisms can be found in biliary cultures of patients on prolonged antibiotics treatment and have stents; however, fungal masses, or balls, are rarely encountered and extremely difficult to eradicate. The aim of this study is to share our experience in fungal cholangitis complicating malignant bile duct obstruction and to reviews reports previously published concerning management of the recurrent obstruction secondary to Candida infections and its correlation with biliary malignancies.

 

Methods: We present our experience with 3 patients who complained of obstructive jaundice. All patients had multiple episodes of fungal cholangitis. Bile samples were obtained during percutaneous trans-hepatic cholangiogram (PTC). Two patients were diagnosed with cholangiocarcinoma and one with adenocarcinoma of the head of the pancreas.

 

Results: Persistent biliary candidiasis may carry a higher morbidity when it rises on the background of biliary malignancy, due to the prolonged course of medical treatment and patient hospitalization, recurrent obstruction with fungus balls, frequent needs to intervene with invasive procedures such as ERCP and PTC and the delay in initiation of chemotherapy.

 

Conclusion: Patients with positive fungal cultures of bile samples obtained by PTC may have coincidental cancers; similar to cholangiocarcinoma, peri-ampullary tumors and gallbladder cancer, therefore, screening with tumor markers, cytology samples and imaging studies is recommended. Aggressive sensitivity-based treatment with systemic antifungals along with external biliary drainage and irrigation with anti-fungals may be necessary for eradication of infection.

  • Liver Diseases
Biography:

Jong-Won Kim is a Ph, D at the Chonbuk National University where he researches pathogenesis of several non-infectious diseases including acute or chronic hepatitis. He holds a B.S. degree in molecular biology and a Doctor of Veterinary pathology from the same university. He has his expertise and tries to clarify the mechanism of non-infectious diseases and contributes to the development of new therapeutic strategies.

Abstract:

Reactive oxygen species (ROS) plays a key role in non-alcoholic steatohepatitis (NASH). Inactivation of glutathione peroxidase-4 (GPX4) induces ferroptosis, which is an iron dependent and lipid peroxidation-mediated non-apoptotic form of cell death. The aim of this study was to investigate the impact of GPX4 on the progression of NASH at an early stage. C57BL6/J mice were fed a methionine and choline-deficient (MCD) diet for 10 days to induce NASH. To determine the role of GPX4 on NASH progression, the inhibitor (RSL-3) and the activator (sodium selenite) of GPX4, the inhibitor of ferroptosis (Liproxstatin-1, Lip-1) and an iron chelator (deferoxamine mesylate salt, DFO) were used in current experiments. RSL-3 treatment showed decreased hepatic expression of GPX4, 12/15-lipoxygenase and apoptosis inducing factor, indicating that GPX4 plays, a key role in NASH-related lipid peroxidation and its-associated cell death. Consistently, serum biochemical analysis showed increased serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels in MCD-fed mice with RSL-3 treatment. In line with these results, NASH-related hepatic steatosis, inflammation and apoptosis were also increased in MCD-fed mice with RSL-3 treatment. However, sodium selenite treatment showed an opposite and protective effect on NASH progression in MCD-fed mice. Administration of DFO showed significantly lowered NASH severity and abolished the harmful effects of RSL-3-mediated GPX4 inhibition in MCD-fed mice. Finally, Lip-1 treatment showed repressed hepatic lipid peroxidation and its associated cell death resulting in decreased NASH severity. Consistent with in vivo findings, similar results were observed in palmitic acid-induced in vitro NASH condition. Taken together, we conclude that ferroptosis might play a major role in development of NASH. These results suggest that modulation of iron-mediated ferroptotic cell death might pave the way for a new strategy in treating NASH.

Biography:

Rays H Y Jiang takes on a pioneer role in establishing a viable research program of genomics in University of South Florida, USA. She has published in high profile journals such as Cell, Science, Nature Communications and Genome Research and secured diverse funding sources from NIH, NSF and Gates’ foundations.

Abstract:

The human liver is the largest internal organ that performs over 500 physiological functions. We used single cell omics to study thousands of primary hepatocytes from human donors with healthy and pathological livers. We also developed specialized computational methods to decode single hepatocyte spatial and temporal information in livers. Our single cell RNAseq analysis revealed enormous transcriptional and biochemical heterogeneity within a single donor liver. We discovered that the principle of essential configuration of maximally incompatible biochemical pathways governs complex liver physiology in the liver lobules. We also studied hepatocyte heterogeneity at single cell level in developmental and cancer livers of humans. Within a hepatocyte cellular carcinoma biopsy sample, there is a continuum of oncogenic transformation degree of hepatocytes, which mirrors the embryonic liver developmental process with the exception of erythropoiesis function. The majority of the tumor derived hepatocytes show properties similar to that of healthy donors, albeit with reduced primary liver functions. Importantly, we found a small group of liver cancer stem cell like progenitors, expressing arrays of embryonic markers such as SOX4, HMGA1 and CXCR1, indicating enhanced onco-genic proliferation potential. Our single cell omics study revealed important temporal and spatial heterogeneity related to liver functions and oncogenic-transformation in humans.

Biography:

Zhuo Wang is a well-qualified, highly skilled and motivated person with more than 8-year work experience in liver disease. She has completed her PhD degree from Hong Kong Polytechnic University in 2014 and currently she is working at Southern University of Science and Technology. Her research focuses on liver fibrosis and liver cancer recently these years.

Abstract:

Hepatocellular carcinoma (HCC) is a long-term sequence of chronic inflammatory liver injury and hepatic injury is associated with a defective intestinal barrier and increased hepatic exposure to bacterial products including lipopolysaccharide (LPS), which promotes hepatocarcinogenesis. Despite its clinical significance, mediators responsible for the high risk of inflammation to develop HCC in the chronically injured liver remain to be clarified. Here, we report a novel mechanism by which LPS/signal transducer and activator of transcription 3 (STAT3) signaling promotes the angiogenesis in HCC both in vitro and in vivo. STAT3 activated by LPS increases the production of vascular endothelial growth factor (VEGF) by tumor cells, which in turn stimulates the migration and tubulogenesis of endothelial cells through STAT3 activation and hence promotes angiogenesis in HCC. Moreover, our data suggested that hypoxia-induced VEGF expression, which also contributes to angiogenesis in HCC, was in a STAT3-dependent pathway. Our findings not only provide a potential mechanism by which bacterial infection enhances HCC oncogenesis through promoting the angiogenesis in liver, but also suggest that targeting STAT3 might be an effective therapeutic strategy in HCC treatment considering the dual roles of STAT3 in angiogenesis.

Biography:

Claudio A is a medical student from University Indonesia. He has won several competitions such as
Scientific Poster in Tarumanegara Medical Competition held by Tarumanegara University and
emergency medical responder held by the National Medical First Responder Team Organization.
He also active in several organization such as First Responder Team in Faculty of Medicine
University of Indonesia and Student Council Organization. As a medical student, he also made a
research and wrote Evidence Based Case Report about Hepatology and interested in that field.

Abstract:

Cirrhosis is an end stage of chronic inflammatory disease with the destruction of liver tissue and
fibrosis that impairs its function to synthesis albumin, prothrombin, and fibrinogen. Cirrhosis can be
detected and classified into 3 groups with non-invasive diagnostic technique by using APRI score.
This study aims to find out the significant difference between albumin, prothrombin time, and
fibrinogen profile within cirrhosis stages based on classification from APRI score. Design of the
study is cross sectional with 60 patients which meet the criteria from the medical records in the
Clinical Pathology Laboratory and center of medical record of RSCM.: The results of the study
were analyzed with Kolmogorov Smirnov test showed albumin level, prothrombin time, and
fibrinogen (median 2.91, 11.8, and mean 273.7117) , Anova or Kruskal Wallis test showed
significant difference between these three components based on score APRI classification. ( all
p<0.05).Then, Post hoc test (Bonferroni for Anova, Mann Whitney for Kruskal Wallis) of
albumin’s profile showed significant difference for comparison between group APRI score less than
0.5 and more than 2. Post hoc test of prothrombin time showed significant difference from all
comparisons. Post hoc test of fibrinogen profile showed significant difference from comparison
between group APRI less than 0.5 and more than 2 ; APRI less 0.5 – 2 and more than 2. As a
results, there are significant difference from comparison between albumin, prothrombin time, and
fibrinogen profile in staging of liver cirrhosis based on classification from APRI score.