scholarly journals AntiGan: An Epinutraceutical Bioproduct with Antitumor Properties in Cultured Cell Lines

Life ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 97
Author(s):  
Olaia Martínez-Iglesias ◽  
Ivan Carrera ◽  
Vinogran Naidoo ◽  
Ramón Cacabelos

Novel and effective chemotherapeutic agents are needed to improve cancer treatment. Epidrugs are currently used for cancer therapy but also exhibit toxicity. Targeting the epigenetic apparatus with bioproducts may aid cancer prevention and treatment. To determine whether the lipoprotein marine extract AntiGan shows epigenetic and antitumor effects, cultured HepG2 (hepatocellular carcinoma) and HCT116 (colorectal carcinoma) cell lines were treated with AntiGan (10, 50, 100, and to 500 µg/mL) for 24 h, 48 h, and 72 h. AntiGan (10 µg/mL) reduced cell viability after 48 h and increased Bax expression; AntiGan (10 and 50 µg/mL) increased caspase-3 immunoreactivity in HepG2 and HCT116 cells. AntiGan (10 and 50 µg/mL) attenuated COX-2 and IL-17 expression in both cell lines. AntiGan (10 µg/mL) increased 5mC levels in both cell types and reduced DNMT1 and DNMT3a expression in these cells. AntiGan (10 and 50 µg/mL) promoted DNMT3a immunoreactivity and reduced SIRT1 mRNA expression in both cell types. In HCT116 cells treated with AntiGan (10 µg/mL), SIRT1 immunoreactivity localized to nuclei and the cytoplasm; AntiGan (50 µg/mL) increased cytoplasmic SIRT1 localization in HCT116 cells. AntiGan is a novel antitumoral bioproduct with epigenetic properties (epinutraceutical) for treating liver and colorectal cancer.

2004 ◽  
Vol 99 (1-3) ◽  
pp. 017-026 ◽  
Author(s):  
Claudia P. Schroeder ◽  
Eva M. Goeldner ◽  
Kai Schulze-Forster ◽  
Christiane A. Eickhoff ◽  
Peter Holtermann ◽  
...  

2013 ◽  
Vol 30 (6) ◽  
pp. 2659-2664 ◽  
Author(s):  
DAISUKE SATO ◽  
YUJI KURIHARA ◽  
SEIJI KONDO ◽  
TATSUO SHIROTA ◽  
YASUO URATA ◽  
...  

2008 ◽  
Vol 29 (6) ◽  
pp. 271-278 ◽  
Author(s):  
Shiro Tochizawa ◽  
Naoya Masumori ◽  
Yoshiaki Yanai ◽  
Yasukazu Ohmoto ◽  
Youichi Yabuuchi ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-13 ◽  
Author(s):  
Fulvia Farabegoli ◽  
Marzia Govoni ◽  
Carmen Ciavarella ◽  
Marina Orlandi ◽  
Alessio Papi

(−)-Epigallocatechin-3-gallate (EGCG) and chemotherapeutic agents cotreatment can improve cytotoxicity against cancer cells. We showed that EGCG and the rexinoid 6-OH-11-O-hydroxyphenanthrene (IIF), given together, were cytotoxic toward MCF-7, MCF-7TAM, and MDA-MB-231, three breast carcinoma cell lines showing different molecular characteristics. Cell growth arrest and apoptosis were greater after EGCG and IIF cotreatment than after individual administration. Cytotoxicity was related to upregulation of 67-kDa laminin receptor (LR67), one of the principal molecular targets of EGCG, and activation of the nuclear retinoic X receptors (RXRs) pathway. Furthermore, the transcription factor Forkhead box O3 (Foxo3a), a protein able to trigger apoptosis through upregulation of genes necessary for cell death, was activated. EGCG and IIF cotreatment produced a significant nuclear import of Foxo3a from the cytoplasm in MCF-7, MCF-7TAM, and MDA-MB-231 cells. In MCF-7TAM cells only, Foxo3a nuclear localization was associated with p473AKT downregulation. For the first time we showed that when EGCG and IIF, two harmless molecules, were given together, they might increase cytotoxicity in three breast carcinoma cell lines, two of them being representative of poorly responsive breast carcinoma types.


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