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Decrease in creatine kinase in human prostatic carcinoma compared to benign prostatic hyperplasia
Cancer Research
|November 1, 1982
Summary
Prostate cancer tissue shows lower creatine kinase activity than benign hyperplasia tissue. This finding suggests creatine kinase may not be a universal marker for prostate cancer tumor burden.
Area of Science:
- Biochemistry
- Oncology
- Urology
Background:
- Elevated creatine kinase (CK) BB isoenzyme activity in peripheral blood has been observed in some prostate cancer patients.
- CK activity is primarily localized to epithelial cells in both hyperplastic and cancerous prostate tissues.
Purpose of the Study:
- To compare creatine kinase activity levels in tissues from benign prostatic hyperplasia and prostate carcinoma.
- To evaluate the potential of creatine kinase as a biomarker for prostate cancer tumor burden.
Main Methods:
- Analysis of creatine kinase activity in tissue samples from 22 patients with benign prostatic hyperplasia and 23 patients with prostate carcinoma.
- Histochemical studies to confirm the cellular localization of creatine kinase activity.
Main Results:
- Prostatic carcinomas exhibited significantly lower creatine kinase activity per gram of tissue compared to prostates with benign prostatic hyperplasia (p < 0.001).
- Despite a larger epithelial component in carcinomas on average, epithelial cells in cancerous tissue contained less CK activity per cell than those in hyperplastic tissue.
- The BB isoenzyme accounted for 98% of CK activity in both cancerous and non-cancerous prostate tissues.
Conclusions:
- Creatine kinase activity is lower in prostate cancer tissue than in benign hyperplastic tissue.
- The significant variability in CK activity among different prostate carcinomas limits its utility as a general marker for tumor burden.
- Longitudinal monitoring of individual patients may be necessary for creatine kinase to be useful in assessing prostate cancer tumor burden.