S19 ribosomal protein dimer augments metal-induced apoptosis in a mouse fibroblastic cell line by ligation of the C5a receptor

2005 ◽  
Vol 94 (3) ◽  
pp. 540-553 ◽  
Author(s):  
Hiroshi Nishiura ◽  
Sumio Tanase ◽  
Yoko Shibuya ◽  
Noriko Futa ◽  
Tamami Sakamoto ◽  
...  

2001 ◽  
Vol 129 (3) ◽  
pp. 445-454 ◽  
Author(s):  
T. Nishimura ◽  
K. Horino ◽  
H. Nishiura ◽  
Y. Shibuya ◽  
T. Hiraoka ◽  
...  


2003 ◽  
Vol 162 (4) ◽  
pp. 1381-1388 ◽  
Author(s):  
Arjun Shrestha ◽  
Megumi Shiokawa ◽  
Takumasa Nishimura ◽  
Hiroshi Nishiura ◽  
Yuji Tanaka ◽  
...  




2008 ◽  
Vol 144 (3) ◽  
pp. 371-381 ◽  
Author(s):  
Y. Oda ◽  
K. Tokita ◽  
Y. Ota ◽  
Y. Li ◽  
K. Taniguchi ◽  
...  


2004 ◽  
Vol 53 (11) ◽  
pp. 623-630 ◽  
Author(s):  
Y. Umeda ◽  
Y. Shibuya ◽  
U. Semba ◽  
K. Tokita ◽  
N. Nishino ◽  
...  


2005 ◽  
Vol 447 (4) ◽  
pp. 747-755 ◽  
Author(s):  
Lei Shi ◽  
Shigeyuki Tsurusaki ◽  
Noriko Futa ◽  
Tamami Sakamoto ◽  
Tomoko Matsuda ◽  
...  


2001 ◽  
Vol 159 (6) ◽  
pp. 2293-2301 ◽  
Author(s):  
Yoko Shibuya ◽  
Megumi Shiokawa ◽  
Hiroshi Nishiura ◽  
Takumasa Nishimura ◽  
Norikazu Nishino ◽  
...  


Author(s):  
Paola Castillo-Juárez ◽  
Sebastián C. Sanchez ◽  
Alma D. Chávez-Blanco ◽  
Humberto Mendoza-Figueroa ◽  
José Correa-Basurto

Background and Objective: Histone deacetylases (HDACs) are important therapeutic targets for many types of human cancers. A derivative of valproic acid, N-(2-hydroxyphenyl)-2-propylpentanamide (HO-AAVPA), has antiproliferative properties on some cancer cell lines and inhibits the HDAC1 isoform. Materials and Methods: In this work, HO-AAVPA was tested as an antiproliferative agent in U87-MG (human glioblastoma) and U-2 OS cells (human osteosarcoma), which are types of cancer that are difficult to treat, and its antiangiogenic properties were explored. Results: HO-AAVPA had antiproliferative effects at 48 h with an IC50 = 0.655 mM in U87-MG cells and an IC50 = 0.453 mM in U-2 OS cells. Additionally, in the colony formation assay, HO-AAVPA decreased the number of colonies by approximately 99% in both cell lines and induced apoptosis by 31.3% in the U-2 OS cell line and by 78.2% in the U87-MG cell line. Additionally, HO-AAVPA reduced the number of vessels in chorioallantoid membranes (CAMs) by approximately 67.74% and IL-6 levels in both cell lines suggesting that the biochemical mechanism on cancer cell of HO-AAVPA is different compared to VPA. Conclusion: HO-AAVPA has antiproliferative effects on glioblastoma and osteosarcoma and antiangiogenic properties.



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