scholarly journals Increased Growth Inhibitory Effects on Human Cancer Cells and Anti-inflammatory Potency of Shogaols from Zingiber officinale Relative to Gingerols

2009 ◽  
Vol 57 (22) ◽  
pp. 10645-10650 ◽  
Author(s):  
Shengmin Sang ◽  
Jungil Hong ◽  
Hou Wu ◽  
Jing Liu ◽  
Chung S. Yang ◽  
...  
2013 ◽  
Vol 76 (6) ◽  
pp. 1078-1084 ◽  
Author(s):  
Laetitia Moreno Y. Banuls ◽  
Ernst Urban ◽  
Michel Gelbcke ◽  
François Dufrasne ◽  
Brigitte Kopp ◽  
...  

2011 ◽  
Vol 35 (6) ◽  
pp. 1561-1567 ◽  
Author(s):  
KUNBO WANG ◽  
ZHONGHUA LIU ◽  
JIANAN HUANG ◽  
ALAA EL-DIN BEKHIT ◽  
FANG LIU ◽  
...  

2011 ◽  
Vol 21 (3) ◽  
pp. 912-915 ◽  
Author(s):  
Zack E. Bryant ◽  
Romy F.J. Janser ◽  
Medina Jabarkhail ◽  
Melissa S. Candelaria-Lyons ◽  
Brittni B. Romero ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (23) ◽  
pp. 7139
Author(s):  
Pedro Novais ◽  
Patrícia M. A. Silva ◽  
Joana Moreira ◽  
Andreia Palmeira ◽  
Isabel Amorim ◽  
...  

Previously, we reported the in vitro growth inhibitory effect of diarylpentanoid BP-M345 on human cancer cells. Nevertheless, at that time, the cellular mechanism through which BP-M345 exerts its growth inhibitory effect remained to be explored. In the present work, we report its mechanism of action on cancer cells. The compound exhibits a potent tumor growth inhibitory activity with high selectivity index. Mechanistically, it induces perturbation of the spindles through microtubule instability. As a consequence, treated cells exhibit irreversible defects in chromosome congression during mitosis, which induce a prolonged spindle assembly checkpoint-dependent mitotic arrest, followed by massive apoptosis, as revealed by live cell imaging. Collectively, the results indicate that the diarylpentanoid BP-M345 exerts its antiproliferative activity by inhibiting mitosis through microtubule perturbation and causing cancer cell death, thereby highlighting its potential as antitumor agent.


Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
SK Lee ◽  
HY Min ◽  
YJ Kang ◽  
JY Hong ◽  
EJ Park ◽  
...  

2014 ◽  
Vol 9 (4) ◽  
pp. 1934578X1400900 ◽  
Author(s):  
Marianna Carbone ◽  
Laura Núñez-Pons ◽  
M. Letizia Ciavatta ◽  
Francesco Castelluccio ◽  
Conxita Avila ◽  
...  

The n-butanol extract of an Antarctic hexactinellid sponge, Anoxycalyx (Scolymastra) joubini, was found to contain a taurine-conjugated anthranilic acid, never reported so far either as a natural product or by synthesis. The compound was inactive against human cancer cells in an in vitro growth inhibitory test, and also showed no antibacterial activity.


Molecules ◽  
2019 ◽  
Vol 24 (2) ◽  
pp. 278 ◽  
Author(s):  
Bu Choi

Apple is a rich source of bioactive phytochemicals that help improve health by preventing and/or curing many disease processes, including cancer. One of the apple polyphenols is phloretin [2′,4′,6′-Trihydroxy-3-(4-hydroxyphenyl)-propiophenone], which has been widely investigated for its antioxidant, anti-inflammatory and anti-cancer activities in a wide array of preclinical studies. The efficacy of phloretin in suppressing xenograft tumor growth in athymic nude mice implanted with a variety of human cancer cells, and the ability of the compound to interfere with cancer cells signaling, have made it a promising candidate for anti-cancer drug development. Mechanistically, phloretin has been reported to arrest the growth of tumor cells by blocking cyclins and cyclin-dependent kinases and induce apoptosis by activating mitochondria-mediated cell death. The blockade of the glycolytic pathway via downregulation of GLUT2 mRNA and proteins, and the inhibition of tumor cells migration, also corroborates the anti-cancer effects of phloretin. This review sheds light on the molecular targets of phloretin as a potential anti-cancer and anti-inflammatory natural agent.


2015 ◽  
Vol 86 ◽  
pp. 16-24 ◽  
Author(s):  
Mariangela Marrelli ◽  
Brigida Cristaldi ◽  
Francesco Menichini ◽  
Filomena Conforti

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