Literature DB >> 21161819

North American cranberry (Vaccinium macrocarpon) stimulates apoptotic pathways in DU145 human prostate cancer cells in vitro.

Malcolm A MacLean1, Bradley E Scott, Bob A Deziel, Melissa C Nunnelley, Anne M Liberty, Katherine T Gottschall-Pass, Catherine C Neto, Robert A R Hurta.   

Abstract

Diets rich in fruits and vegetables have been shown to improve patient prognosis in a variety of cancers, a benefit partly derived from phytochemicals, many of which target cell death pathways in tumor cells. Cranberries (Vaccinium macrocarpon) are a phytochemical-rich fruit containing a variety of polyphenolic compounds. As flavonoids have been shown to induce apoptosis in human tumor cells, this study investigated the hypothesis that cranberry-mediated cytotoxicity in DU145 human prostate adenocarcinoma cells involves apoptosis. The results showed that induction of apoptosis in these cells occurred in response to treatment with whole cranberry extract and occurred through caspase-8 mediated cleavage of Bid protein to truncated Bid resulting in cytochrome-C release from the mitochondria. Subsequent activation of caspase-9 ultimately resulted in cell death as characterized by DNA fragmentation. Increased Par-4 protein expression was observed, and this is suggested to be at least partly responsible for caspase-8 activation. Proanthocyanidin-enriched and flavonol-enriched fractions of cranberry also increased caspase-8 and caspase-9 activity, suggesting that these compounds play a possible role in apoptosis induction. These findings indicate that cranberry phytochemicals can induce apoptosis in prostate cancer cells in vitro, and these findings further establish the potential value of cranberry phytochemicals as possible agents against prostate cancer.

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Year:  2011        PMID: 21161819     DOI: 10.1080/01635581.2010.516876

Source DB:  PubMed          Journal:  Nutr Cancer        ISSN: 0163-5581            Impact factor:   2.900


  8 in total

1.  Effects of cranberry extracts on gene expression in THP-1 cells.

Authors:  Daniel B Hannon; Jerry T Thompson; Christina Khoo; Vijaya Juturu; John P Vanden Heuvel
Journal:  Food Sci Nutr       Date:  2016-04-25       Impact factor: 2.863

2.  Dietary feeding of freeze-dried whole cranberry inhibits intestinal tumor development in Apcmin/+ mice.

Authors:  Duochen Jin; Tianyu Liu; Wenxiao Dong; Yujie Zhang; Sinan Wang; Runxiang Xie; Bangmao Wang; Hailong Cao
Journal:  Oncotarget       Date:  2017-10-26

3.  Cranberry proanthocyanidins modulate reactive oxygen species in Barrett's and esophageal adenocarcinoma cell lines.

Authors:  Katherine M Weh; Harini S Aiyer; Amy B Howell; Laura A Kresty
Journal:  J Berry Res       Date:  2016       Impact factor: 2.352

Review 4.  Prostate apoptosis response-4 and tumor suppression: it's not just about apoptosis anymore.

Authors:  Anees Rahman Cheratta; Faisal Thayyullathil; Siraj Pallichankandy; Karthikeyan Subburayan; Ameer Alakkal; Sehamuddin Galadari
Journal:  Cell Death Dis       Date:  2021-01-07       Impact factor: 8.469

5.  Proanthocyanidin-enriched cranberry extract induces resilient bacterial community dynamics in a gnotobiotic mouse model.

Authors:  Catherine C Neto; Benedikt M Mortzfeld; John R Turbitt; Shakti K Bhattarai; Vladimir Yeliseyev; Nicholas DiBenedetto; Lynn Bry; Vanni Bucci
Journal:  Microb Cell       Date:  2021-04-29

6.  Prostate apoptosis response-4 is involved in the apoptosis response to docetaxel in MCF-7 breast cancer cells.

Authors:  Michelly C Pereira; Simone A de Bessa-Garcia; Ravshan Burikhanov; Ana Carolina Pavanelli; Lourival Antunes; Vivek M Rangnekar; Maria A Nagai
Journal:  Int J Oncol       Date:  2013-06-12       Impact factor: 5.650

Review 7.  Cranberries and Cancer: An Update of Preclinical Studies Evaluating the Cancer Inhibitory Potential of Cranberry and Cranberry Derived Constituents.

Authors:  Katherine M Weh; Jennifer Clarke; Laura A Kresty
Journal:  Antioxidants (Basel)       Date:  2016-08-18

8.  Cranberry extract initiates intrinsic apoptosis in HL-60 cells by increasing BAD activity through inhibition of AKT phosphorylation.

Authors:  Rasha A Mansouri; Susan S Percival
Journal:  BMC Complement Med Ther       Date:  2020-03-06
  8 in total

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