Gastric Cancer in the Era of Precision Medicine

Autor: Stephen J. Meltzer, Xi Liu
Rok vydání: 2017
Předmět:
0301 basic medicine
Biomarker identification
Preclinical Models
MSI
microsatellite unstable/instability

MSS/EMT
microsatellite stable with epithelial-to-mesenchymal transition features

MSI-H
high microsatellite instability

Review
Biology
Bioinformatics
Genome
Molecular Classification
03 medical and health sciences
Cancer Genomics
GTPase
guanosine triphosphatase

Genetic Evolution
miRNA
microRNA

medicine
CIN
chromosomally unstable/chromosomal instability

LOH
loss of heterozygosity

TGF
transforming growth factor

Cancer death
EBV
Epstein-Barr virus

Hepatology
business.industry
GAPPS
gastric adenocarcinoma and proximal polyposis of the stomach

Gastroenterology
Cancer
Precision medicine
medicine.disease
HDGC
hereditary diffuse gastric cancer

PDX
patient-derived tumor xenografts

NGS
next-generation sequencing

Gastric Cancer
hPSC
human pluripotent stem cell

030104 developmental biology
CIMP
CpG island methylator phenotype

GC
gastric cancer

TCGA
The Cancer Genome Atlas

lncRNA
long noncoding RNA

Personalized medicine
business
EBV - Epstein-Barr virus
Zdroj: Cellular and Molecular Gastroenterology and Hepatology
ISSN: 2352-345X
DOI: 10.1016/j.jcmgh.2017.02.003
Popis: Gastric cancer (GC) remains the third most common cause of cancer death worldwide, with limited therapeutic strategies available. With the advent of next-generation sequencing and new preclinical model technologies, our understanding of its pathogenesis and molecular alterations continues to be revolutionized. Recently, the genomic landscape of GC has been delineated. Molecular characterization and novel therapeutic targets of each molecular subtype have been identified. At the same time, patient-derived tumor xenografts and organoids now comprise effective tools for genetic evolution studies, biomarker identification, drug screening, and preclinical evaluation of personalized medicine strategies for GC patients. These advances are making it feasible to integrate clinical, genome-based and phenotype-based diagnostic and therapeutic methods and apply them to individual GC patients in the era of precision medicine.
Databáze: OpenAIRE