scholarly journals A NOTCH-sensitive uPAR-regulated oncolytic adenovirus effectively suppresses pancreatic tumor growth and triggers synergistic anticancer effects with gemcitabine and nab-paclitaxel

Oncotarget ◽  
2017 ◽  
Vol 8 (14) ◽  
pp. 22700-22715 ◽  
Author(s):  
Ana Mato-Berciano ◽  
Giulia Raimondi ◽  
Maria Victoria Maliandi ◽  
Ramon Alemany ◽  
Lluis Montoliu ◽  
...  
2010 ◽  
Vol 48 (08) ◽  
Author(s):  
N Azoitei ◽  
GV Pusapati ◽  
A Kleger ◽  
C Brunner ◽  
F Genze ◽  
...  

2012 ◽  
Vol 38 (12) ◽  
pp. 1121-1131
Author(s):  
Xiao-Hui WANG ◽  
Ya-Min ZHENG ◽  
Ye-Qing CUI ◽  
Shuang LIU ◽  
Hai-Chen SUN ◽  
...  

2021 ◽  
Author(s):  
I Pozios ◽  
E Günzler ◽  
N Hering ◽  
M Arndt ◽  
C Kamphues ◽  
...  

2010 ◽  
Vol 78 (2) ◽  
pp. 226-236 ◽  
Author(s):  
Indira Jutooru ◽  
Gayathri Chadalapaka ◽  
Maen Abdelrahim ◽  
Md Riyaz Basha ◽  
Ismael Samudio ◽  
...  

2007 ◽  
Vol 15 (2) ◽  
pp. 295-302 ◽  
Author(s):  
Ji Young Yoo ◽  
Joo-Hang Kim ◽  
Young-Guen Kwon ◽  
Eok-Cheon Kim ◽  
Nam Kyu Kim ◽  
...  

2008 ◽  
Vol 68 (11) ◽  
pp. 4360-4368 ◽  
Author(s):  
Hongkui Jin ◽  
Renhui Yang ◽  
Zhong Zheng ◽  
Mally Romero ◽  
Jed Ross ◽  
...  

Cancers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1412
Author(s):  
Chang Woo Han ◽  
Mi Suk Jeong ◽  
Sung Chul Ha ◽  
Se Bok Jang

Kirsten-RAS (KRAS) has been the target of drugs because it is the most mutated gene in human cancers. Because of the low affinity of drugs for KRAS mutations, it was difficult to target these tumor genes directly. We found a direct interaction between KRAS G12V and tumor suppressor novel H-REV107 peptide with high binding affinity. We report the first crystal structure of an oncogenic mutant, KRAS G12V-H-REV107. This peptide was shown to interact with KRAS G12V in the guanosine diphosphate (GDP)-bound inactive state and to form a stable complex, blocking the activation function of KRAS. We showed that the peptide acted as an inhibitor of mutant KRAS targets by [α-32P] guanosine triphosphate (GTP) binding assay. The H-REV107 peptide inhibited pancreatic cancer and colon cancer cell lines in cell proliferation assay. Specially, the H-REV107 peptide can suppress pancreatic tumor growth by reduction of tumor volume and weight in xenotransplantation mouse models. Overall, the results presented herein will facilitate development of novel drugs for inhibition of KRAS mutations in cancer patients.


2020 ◽  
Vol 401 ◽  
pp. 115118
Author(s):  
Ye Yao ◽  
Qing-yu Yao ◽  
Jun-sheng Xue ◽  
Xiu-yun Tian ◽  
Qi-ming An ◽  
...  

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