Evidence of an inhibitory effect of diet and exercise on prostate cancer cell growth

Citation
Cn. Tymchuk et al., Evidence of an inhibitory effect of diet and exercise on prostate cancer cell growth, J UROL, 166(3), 2001, pp. 1185-1189
Citations number
24
Categorie Soggetti
Urology & Nephrology","da verificare
Journal title
JOURNAL OF UROLOGY
ISSN journal
00225347 → ACNP
Volume
166
Issue
3
Year of publication
2001
Pages
1185 - 1189
Database
ISI
SICI code
0022-5347(200109)166:3<1185:EOAIEO>2.0.ZU;2-C
Abstract
Purpose: A high fat diet and sedentary lifestyle may predispose men to pros tate cancer through effects on serum factors such as hormones. We evaluated the effects of a low fat, high fiber diet and exercise intervention on ser um stimulated growth of established prostate cancer cell lines. Materials and Methods: Fasting serum was obtained from 13 overweight men be fore and after undergoing an 11-day low fat, high fiber diet and exercise i ntervention. Serum was also obtained from 8 men who had complied with the r egimen for a mean of 14.2 years. Hormone dependent LNCaP and independent PC -3 prostate cancer cell lines were grown in culture medium containing 10% o f subject pre-intervention or post-intervention serum and viable cells were counted after 48 hours. Anthropometry, serum free testosterone, lipids and glucose were measured in all subjects. Results: Post-intervention serum from each of the 11-day intervention subje cts reduced LNCaP cell growth by a mean of 30% compared with pre-interventi on serum from each (p < 0.01). LNCaP cell growth in serum from long-term su bjects was 15% below that of post-intervention serum (p < 0.01). There was no difference in the growth of PC-3 cells when cultured with serum from eit her intervention group. Serum free testosterone, body weight, glucose and l ipids were significantly reduced in 11-day subjects. Conclusions: A low fat, high fiber diet and exercise intervention resulted in serum changes that significantly reduced the growth of androgen responsi ve LNCaP prostate cancer cells in vitro.