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Isolation of Cancer Stem Cells From Human Prostate Cancer Samples
Published on: March 14, 2014
Abiraterone acetate in the treatment of prostate cancer
Abhimanyu Thakur1, Aishwarya Roy1, Arijit Ghosh2
1Department of Pharmaceutical Sciences & Technology, Birla Institute of Technology Mesra, India.
Abstract:
Among all cancer-related death, prostate cancer accounts for the second prominent reason for cancer-associated death in men. Despite the castration mediated reduction in testosterone synthesis, adrenal glands, as well as tissues of prostate cancer, continue to produce androgens, which ultimately lead to the growth of prostate cancer. This phase is referred as metastatic castration-resistant prostate cancer, which throws an obstacle to treatment. Androgen antagonists, in addition to deprivation of hormone, is being used for reducing the level of prostate-specific antigen but has not successfully come in front as a choice for prolonging the life of patients suffering from prostate cancer. In this prevailing scenario, abiraterone acetate (AA) has proved to be a boon for patients suffering from prostate cancer. AA selectively inhibits the actions of enzymes C17, 20-lyase and 17α-hydroxylase on cytochrome P450 (CYP) 17 when administered orally. The signaling of androgen receptor, being important for primary to metastatic phases of prostate cancer, CYP17 is essential for the synthesis of androgen. Herein, the in-detail pharmacological profile of AA, including androgen signaling, mechanism of action of AA, mechanism of AA resistance, pharmacokinetics, latest clinical findings, predictive markers, optimal treatment sequence, toxicity, and food interaction profiles have been reviewed.
Insights
Abiraterone acetate (AA) offers a new treatment for metastatic castration-resistant prostate cancer by inhibiting androgen synthesis. This review details its pharmacology, clinical use, and resistance mechanisms for prostate cancer patients.
Area of Science:
- Oncology
- Pharmacology
Background:
- Prostate cancer is a leading cause of cancer death in men.
- Metastatic castration-resistant prostate cancer (mCRPC) poses treatment challenges due to continued androgen production.
- Current treatments like androgen antagonists have limited efficacy in prolonging patient survival.
Purpose of the Study:
- To provide a comprehensive pharmacological profile of abiraterone acetate (AA).
- To review AA's mechanism of action, resistance, pharmacokinetics, clinical findings, and toxicity.
- To discuss predictive markers and optimal treatment sequencing for AA in prostate cancer.
Main Methods:
- Review of abiraterone acetate's selective inhibition of CYP17 enzymes (17α-hydroxylase and C17, 20-lyase).
- Analysis of androgen receptor signaling pathways in prostate cancer progression.
- Compilation of data on clinical efficacy, pharmacokinetics, and safety of AA.
Main Results:
- Abiraterone acetate effectively inhibits androgen synthesis essential for prostate cancer growth.
- The review covers AA's mechanism of action, resistance, pharmacokinetics, and clinical outcomes.
- Toxicity, food interactions, and predictive markers are discussed for optimal patient management.
Conclusions:
- Abiraterone acetate represents a significant advancement in treating metastatic castration-resistant prostate cancer.
- Understanding AA's profile aids in optimizing treatment strategies and managing resistance.
- Further research into predictive markers and treatment sequences will enhance its clinical utility.
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