Published online May 31, 2006.
https://doi.org/10.4111/kju.2006.47.5.467
The Effects of GAC on the Biochemical Profiles and Quality of Life of Metastatic Prostate Cancer Patients
Abstract
Purpose
In order to evaluate the effects of GAC, which is the combination of active hexose correlated compound (AHCC) and genistein combined polysaccharide (GCP), we investigated the changes in the biochemical profiles and the quality of life of prostate cancer patients with androgen suppression after the administration of GAC.
Materials and Methods
Thirty two eligible metastatic prostate cancer patients between the ages of 54 and 84 were enrolled in this study, and they were supplemented with 5g GAC per day (n=23) or placebo (n=9) for a 6 months period. Blood and urine sample analysis were taken and the quality of life (QoL) was assessed using the Visual Analogue Scale (VAS) and the Functional Assessment of Cancer Therapy Scale Questionnaire (FACT-G) at baseline and at post intervention (after 3 and 6 months).
Results
Twenty six patients (n=18 in the GAC group and n=8 in the placebo group) completed the 6 months intervention. No statistically significant adverse events were reported by the study participants. GAC had no significant effect on the serum biochemical parameters. However, all 7 GAC-treated hypercholesterolemic patients had their cholesterol level decreased after 3 months treatment (p<0.02). Results of Comet assay showed significant decreases in tail moment (p<0.009) and tail length (p<0.004) at 6 months compared to baseline for the GAC group. Although the results of the VAS were inconsistent, the score for physical well-being was increased in GAC group on the FACT-G analysis (p<0.05 between baseline and 3 months, respectively).
Conclusions
Oral administration of GAC 5g per day for 6 months showed a decrease in DNA damage of blood lymphocytes and in the total serum cholesterol level in hypercholesterolemic patients without any significant influences on the serum biochemical parameters of the metastatic prostate cancer patients. Further studies on the role of GAC are necessary to clarify the advantage of GAC supplementation in prostate cancer patients with androgen suppression.
Fig. 1
Changes in the concentration of the total cholesterol in the serum of the GAC supplement patients with hypercholesterolemia. *p<0.02 for comparing the initial mean and the 3 months' mean by using the Wilcoxon signed rank test.
Table 1
General characteristics of the subjects at baseline
Table 2
Changes in the intake and urinary excretion of isoflavones in the placebo group and the genistein combined polysaccharide (GCP) and active hexose correlated compound (AHCC) mixture/GAC supplement group at baseline, 3 months and 6 months
Table 3
Changes in the blood and serum biochemical characteristics
Table 4
Lymphocyte DNA damage using comet assay in the placebo group and the GAC supplement group
Table 5
Changes of the pain score in the placebo group and the GAC supplement group
Table 6
Changes of the FACT-G subscale and the overall scores
References
-
Stege R. Potential side-effects of endocrine treatment of long duration in prostate cancer. Prostate 2000;10 Suppl:38–42.
-
-
Hong SJ, Kim SI, Kwon SM, Lee JR, Chung BC. Comparative study of concentration of isoflavones and lignans in plasma and prostatic tissues of normal control and benign prostatic hyperplasia. Yonsei Med J 2002;43:235–241.
-
-
Yagita A, Maruyama S, Wakasugi S, Sukegawa Y. H-2 haplotype-dependent serum IL-12 production in tumor-bearing mice treated with various mycelial extracts. In Vivo 2002;16:49–54.
-
-
Lin AD, Chen KK, Lin AT, Chang YH, Wu HH, Kuo JY, et al. Antiandrogen-associated hepatotoxicity in the management of advanced prostate cancer. J Chin Med Assoc 2003;66:735–740.
-
-
Betti C, Davini T, Giannessi L, Loprieno N, Barale R. Micro gel electorphoresis assay (comet assay) and SCE analysis in human lymphocytes from 100 normal subjects. Mutat Res 1994;307:323–333.
-
-
Xu X, Harris KS, Wang HJ, Murphy PA, Hendrich S. Bioavilability of soybean isoflavones depends upon gut microflora in women. J Nutr 1995;125:2307–2315.
-
-
Demark-Wahnefried W, Price DT, Polascik TJ, Robertson CN, Anderson EE, Walther PJ, et al. Pilot study of dietary fat restriction and flaxseed supplementation in men with prostate cancer before surgery: exploring the effects on hormonal levels, prostate-specific antigen, and histopathologic features. Urology 2001;58:47–52.
-
-
Hong SJ, Kim JS, Lee MJ, Yoon S, Lee JM, Oh HY. The effect of isoflavone intake on serum biochemical profiles and antioxidant system in patients with prostatic Diseases. Korean J Urol 2005;46:360–365.
-
-
Zhuang L, Kim J, Adam RM, Solomon KR, Freeman MR. Cholesterol targeting alters lipid raft composition and cell survival in prostate cancer cells and xenografts. J Cin Invest 2005;115:959–968.
-