Resveratrol Exerts Differential Effects in Vitro and in Vivo against Ovarian Cancer Cells

被引:27
作者
Stakleff, Kimberly Sloan [2 ]
Sloan, Tricia [2 ]
Blanco, Denise [2 ]
Marcanthony, Sharon [3 ]
Booth, Tristan D. [4 ]
Bishayee, Anupam [1 ]
机构
[1] Amer Univ Hlth Sci, Sch Pharm, Dept Pharmaceut & Adm Sci, Signal Hill, CA USA
[2] Akron Gen Med Ctr, Kenneth Calhoun Res Lab, Akron, OH USA
[3] Akron Gen Med Ctr, Dept Obstet & Gynecol, Akron, OH USA
[4] Pharmascience Inc, Clin & Innovat Dev, Montreal, PQ, Canada
关键词
Resveratrol; NuTu-19; cells; ovarian cancer; anti-invasion effects; chemoprevention; ABERRANT CRYPT FOCI; ANTICANCER ACTIVITY; NATURAL-PRODUCTS; GENE-EXPRESSION; CARCINOMA CELLS; FISCHER-344; RAT; ANIMAL-MODEL; NUDE-MICE; PREVENTION; APOPTOSIS;
D O I
10.7314/APJCP.2012.13.4.1333
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epithelial ovarian cancer represents the most lethal gynecological cancer, and the high mortality rate makes this malignancy a major health concern. Poor prognosis results from an inability to detect ovarian cancers at an early, curable stage, as well as from the lack of an effective therapy. Thus, effective and novel strategies for prevention and treatment with non-toxic agents merit serious consideration. Resveratrol, obtained from grapes, berries, peanuts and red wine, has been shown to have a potent growth-inhibitory effect against various human cancer cells as well as in in vivo preclinical cancer models. The objective here was to evaluate potential antitumor effects of resveratrol in both in vitro and in vivo NuTu-19 ovarian cancer models. In vitro an invasion assay was performed. After 48 h, the numbers of viable cells that invaded the extracellular matrix layer were reduced by 94% with resveratrol in comparison to control. For the in vivo anti-tumor assessment, 10 rats were injected with NuTu-19 cells into the ovarian bursa. Thereafter, half were provided with a diet mixed with a dose of 100 mg resveratrol/kg body weight/day for 28 days. Following sacrifice, anticancer effects were assessed by histological evaluation of ovarian as well as surrounding tissues, and immunohistochemical detection of cell proliferation and apoptosis, but there were no observable differences between the control and resveratrol-treated groups for any of the biological endpoints. While resveratrol is effective in suppressing the in vitro cellular invasion of NuTu-19 ovarian cancer cells, these effects do not appear to impact on in vivo NuTu-19 ovarian cancers in rats.
引用
收藏
页码:1333 / 1340
页数:8
相关论文
共 62 条
[1]   PERIODIC ACID-SCHIFF STAIN AS A PROGNOSTIC INDICATOR IN SEROUS AND MUCINOUS OVARIAN-TUMORS [J].
AALTO, ML ;
COLLAN, Y .
INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 1986, 24 (01) :27-34
[2]  
Aggarwal BB, 2004, ANTICANCER RES, V24, P2783
[3]   Multiple molecular targets of resveratrol: Anti-carcinogenic mechanisms [J].
Athar, Mohammad ;
Back, Jung Ho ;
Kopelovich, Levy ;
Bickers, David R. ;
Kim, Arianna L. .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2009, 486 (02) :95-102
[4]  
Banerjee S, 2002, CANCER RES, V62, P4945
[5]   Genetically engineered models have advantages over xenografts for preclinical studies [J].
Becher, OJ ;
Holland, EC .
CANCER RESEARCH, 2006, 66 (07) :3355-3358
[6]   Current Advances in Cancer Prevention and Treatment by Natural Products [J].
Bishayee, Anupam .
CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2012, 13 (01) :115-116
[8]   Resveratrol-mediated chemoprevention of diethylnitrosamine-initiated hepatocarcinogenesis: Inhibition of cell proliferation and induction of apoptosis [J].
Bishayee, Anupam ;
Dhir, Neetika .
CHEMICO-BIOLOGICAL INTERACTIONS, 2009, 179 (2-3) :131-144
[9]   Resveratrol induces SIRT1-and energy-stress-independent inhibition of tumor cell regrowth after low-dose platinum treatment [J].
Bjorklund, My ;
Roos, Jeanette ;
Gogvadze, Vladimir ;
Shoshan, Maria .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2011, 68 (06) :1459-1467
[10]   Effect of resveratrol on growth of 4T1 breast cancer cells in vitro and in vivo [J].
Bove, K ;
Lincoln, DW ;
Tsan, MF .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 291 (04) :1001-1005