scholarly journals Decoding the anticancer activity of VO-clioquinol compound: the mechanism of action and cell death pathways in human osteosarcoma cells

Metallomics ◽  
2017 ◽  
Vol 9 (7) ◽  
pp. 891-901 ◽  
Author(s):  
Ignacio E. León ◽  
Paula Díez ◽  
Enrique J. Baran ◽  
Susana B. Etcheverry ◽  
Manuel Fuentes

Vanadium compounds were studied in recent years by considering them as a representative of a new class of non-platinum metal anticancer drugs.


2013 ◽  
Vol 12 (3) ◽  
pp. 314-325 ◽  
Author(s):  
Joe Hasei ◽  
Tsuyoshi Sasaki ◽  
Hiroshi Tazawa ◽  
Shuhei Osaki ◽  
Yasuaki Yamakawa ◽  
...  




2009 ◽  
Vol 23 (7) ◽  
pp. 1268-1276 ◽  
Author(s):  
Ko-Long Lin ◽  
Chorng-Chih Huang ◽  
Jin-Shiung Cheng ◽  
Jeng-Yu Tsai ◽  
Yih-Chau Lu ◽  
...  


Autophagy ◽  
2008 ◽  
Vol 4 (8) ◽  
pp. 1020-1033 ◽  
Author(s):  
Stefania Meschini ◽  
Maria Condello ◽  
Annarica Calcabrini ◽  
Manuela Marra ◽  
Giuseppe Formisano ◽  
...  


2010 ◽  
Vol 27 (1) ◽  
pp. 53-62 ◽  
Author(s):  
Takeshi Hori ◽  
Takashi Kondo ◽  
Hyemi Lee ◽  
Chang W. Song ◽  
Heon Joo Park


2012 ◽  
Vol 29 (9) ◽  
pp. 1020-1031 ◽  
Author(s):  
Ching-Lung Liao ◽  
Shu-Chun Hsu ◽  
Chien-Chih Yu ◽  
Jai-Sing Yang ◽  
Nou-Ying Tang ◽  
...  


Toxicology ◽  
2007 ◽  
Vol 231 (1) ◽  
pp. 21-29 ◽  
Author(s):  
Shu-Shong Hsu ◽  
Chun-Jen Huang ◽  
He-Hsiung Cheng ◽  
Chiang-Ting Chou ◽  
Hsiao-Ying Lee ◽  
...  


2020 ◽  
Vol 2020 ◽  
pp. 1-23
Author(s):  
Huanhuan Lv ◽  
Chenxiao Zhen ◽  
Junyu Liu ◽  
Peng Shang

Osteosarcoma is the most common primary malignancy of the skeleton in children and adults. The outcomes of people with osteosarcomas are unsatisfied. β-Phenethyl isothiocyanate (PEITC) exhibits chemoprevention and chemotherapeutic activities against many human cancers. The molecular mechanism underlying its action on osteosarcoma is still unknown. This study was aimed at investigating the effect of PEITC on human osteosarcoma both in vitro and in vivo. The results showed that PEITC reduced cell viability, inhibited proliferation, and caused G2/M cell cycle arrest in four human osteosarcoma cell lines (MNNG/HOS, U-2 OS, MG-63, and 143B). Then, we found that PEITC altered iron metabolism related to the processes of iron import, storage, and export, which resulted in increased labile iron. Expectedly, PEITC caused oxidative stress as a consequence of GSH depletion-inducing ROS generation and lipid peroxidation. Multiple cell death modalities, including ferroptosis, apoptosis, and autophagy, were triggered in human osteosarcoma cells. Three MAPKs (ERK, p38, and JNK) were all activated after PEITC treatment; however, they presented different responses among the four human osteosarcoma cell lines. ROS generation was proved to be the major cause of PEITC-induced decreased proliferative potential, altered iron metabolism, cell death, and activated MAPKs in human osteosarcoma cells. In addition, PEITC also significantly delayed tumor growth in a xenograft osteosarcoma mouse model with a 30 mg/kg administration dose. In conclusion, this study reveals that PEITC simultaneously triggers ferroptosis, apoptosis, and autophagy in human osteosarcoma cells by inducing oxidative stress.



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