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Genome-wide CRISPR screen reveals a druggable target of sorafenib | 38947
Internal Medicine: Open Access

Internal Medicine: Open Access
Open Access

ISSN: 2165-8048

+44 1300 500008

Genome-wide CRISPR screen reveals a druggable target of sorafenib in hepatocellular carcinoma


2nd International Conference on Internal Medicine & Hospital Medicine

September 13-14, 2017 Dallas, USA

Weijian Sun

Yuying Children��?s Hospital of Wenzhou Medical University, China

Keynote: Intern Med

Abstract :

HCC is the most common reasons of cancer related death, due to its resistance to chemotherapy. Sorafenib is currently the only approved systemic drug for patients with advanced HCC. Unfortunately, sorafenib treatment allows only the increase of patients��? survival in a few months, new therapeutic targets are urgently needed. Scientists establish CRISPR/Cas9 system as a powerful tool for systematic genetic analysis in mammalian. At present, no clearly predictive biomarkers have been identified to guide sorafenib treatment with advanced hepatocellular carcinoma. Our study demonstrates that CRISPR/ Cas9-mediated genome editing in combination with next-generation sequencing (NGS) as a powerful tool to find biomarkers of sorafenib to guide treatment. Our date confirmed SGOL1 are sorafenib druggable target gene, and a strong expression of SGOL1 is correlated with a lower overall survival rate of HCC patients after hepatectomy. To our knowledge, this study is the first time to utilize genome-wide CRISPR screens for identify a predictive biomarker that can be used to select patients who are most likely to benefit from sorafenib treatment.

Biography :

Weijian Sun is a PhD holder at School of Medicine, Zhejiang University. He is the Associate Chief Physician of the second affiliated hospital and Yuying Children’s Hospital of Wenzhou Medical University.

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