Identification of predictive response and resistance factors to targeted therapy in gastric cancer using a systems medicine approach

2016 ◽  
Vol 69 ◽  
pp. S135
Author(s):  
B. Luber ◽  
S. Keller ◽  
G. Zwingenberger ◽  
K. Ebert ◽  
D. Maier ◽  
...  
2021 ◽  
Author(s):  
Yanpeng Ma ◽  
Wenyao Wang ◽  
Longlong Liu ◽  
Yang liu ◽  
Wei Bi

Background: This study aims to investigate the correlation of VEGF-B and FLT-1 co-expression with the prognosis of gastric cancer (GC). Materials & methods: Primary GC samples and adjacent tissues were obtained from 96 patients. Results: Both VEGF-B and FLT-1 were testified to be upregulated in the human GC compared with adjacent tissues. Spearman’s rank correlation analysis indicated that VEGF-B and FLT-1 expression were correlated (r = 0.321, p = 0.0015). High VEGF-B and FLT-1 co-expression patients showed poor prognosis when compared with low VEGF-B and FLT-1 co-expression patients (p = 0.0169). Conclusion: The high co-expression of VEGF-B and FLT-1 in GC shows a poor prognosis of overall survival, and targeted therapy against the interaction between VEGF-B and FLT-1 is worth further detailed analysis.


2015 ◽  
pp. 317-330
Author(s):  
Georgios D. Lianos ◽  
Alberto Mangano ◽  
Stefano Rausei ◽  
Aikaterini Lianou ◽  
Zoi Anastasiadi ◽  
...  

2015 ◽  
Vol 19 (3) ◽  
pp. 687-695 ◽  
Author(s):  
Hisato Kawakami ◽  
Isamu Okamoto

Epigenomics ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 1477-1497 ◽  
Author(s):  
Sadegh Fattahi ◽  
Monireh Golpour ◽  
Fatemeh Amjadi-Moheb ◽  
Marzieh Sharifi-Pasandi ◽  
Parastesh Khodadadi ◽  
...  

Bioengineered ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 6343-6353
Author(s):  
Mingzhen Lin ◽  
Wenxia Yao ◽  
Yao Xiao ◽  
Zhijie Dong ◽  
Wei Huang ◽  
...  

Cancers ◽  
2021 ◽  
Vol 13 (20) ◽  
pp. 5216
Author(s):  
Justus Körfer ◽  
Florian Lordick ◽  
Ulrich T. Hacker

Gastric cancer is a leading cause of cancer death worldwide. Systemic treatment comprising chemotherapy and targeted therapy is the standard of care in advanced/metastatic gastric cancer. Comprehensive molecular characterization of gastric adenocarcinomas by the TCGA Consortium and ACRG has resulted in the definition of distinct molecular subtypes. These efforts have in parallel built a basis for the development of novel molecularly stratified treatment approaches. Based on this molecular characterization, an increasing number of specific genomic alterations can potentially serve as treatment targets. Consequently, the development of promising compounds is ongoing. In this review, key molecular alterations in gastric and gastroesophageal junction cancers will be addressed. Finally, the current status of the translation of targeted therapy towards clinical applications will be reviewed.


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