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Microarray-based Identification of Individual HERV Loci Expression: Application to Biomarker Discovery in Prostate Cancer
Published on: November 2, 2013
New insights into molecular signaling pathways and current advancements in prostate cancer diagnostics & therapeutics
Neha Thakur1, Sameer Quazi2,3,4,5,6, Bindu Naik7
1Department of Biotechnology, Graphic Era (Deemed to be University), Dehradun, Uttarakhand, India.
Abstract:
Prostate adenocarcinoma accounts for more than 20% of deaths among males due to cancer. It is the fifth-leading cancer diagnosed in males across the globe. The mortality rate is quite high due to prostate cancer. Despite the fact that advancements in diagnostics and therapeutics have been made, there is a lack of effective drugs. Metabolic pathways are altered due to the triggering of androgen receptor (AR) signaling pathways, and elevated levels of dihydrotestosterone are produced due to defects in AR signaling that accelerate the growth of prostate cancer cells. Further, PI3K/AKT/mTOR pathways interact with AR signaling pathway and act as precursors to promote prostate cancer. Prostate cancer therapy has been classified into luminal A, luminal B, and basal subtypes. Therapeutic drugs inhibiting dihydrotestosterone and PI3K have shown to give promising results to combat prostate cancer. Many second-generation Androgen receptor signaling antagonists are given either as single agent or with the combination of other drugs. In order to develop a cure for metastasized prostate cancer cells, Androgen deprivation therapy (ADT) is applied by using surgical or chemical methods. In many cases, Prostatectomy or local radiotherapy are used to control metastasized prostate cancer. However, it has been observed that after 1.5 years to 2 years of Prostatectomy or castration, there is reoccurrence of prostate cancer and high incidence of castration resistant prostate cancer is seen in population undergone ADT. It has been observed that Androgen derivation therapy combined with drugs like abiraterone acetate or docetaxel improve overall survival rate in metastatic hormone sensitive prostate cancer (mHSPC) patients. Scientific investigations have revealed that drugs inhibiting poly ADP Ribose polymerase (PARP) are showing promising results in clinical trials in the prostate cancer population with mCRPC and DNA repair abnormalities. Recently, RISUG adv (reversible inhibition of sperm under guidance) has shown significant results against prostate cancer cell lines and MTT assay has validated substantial effects of this drug against PC3 cell lines. Current review paper highlights the advancements in prostate cancer therapeutics and new drug molecules against prostate cancer. It will provide detailed insights on the signaling pathways which need to be targeted to combat metastasized prostate cancer and castration resistant prostate cancer.
Insights
Prostate cancer, a leading cause of male deaths, lacks effective drugs. New therapies targeting androgen receptor and PI3K pathways, including PARP inhibitors and RISUG adv, show promise against advanced and castration-resistant prostate cancer.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Prostate adenocarcinoma is a significant cause of cancer-related mortality in males globally.
- Despite advancements, effective therapeutic options for advanced and castration-resistant prostate cancer remain limited.
- Androgen receptor (AR) signaling and associated metabolic pathways, like PI3K/AKT/mTOR, are crucial in prostate cancer progression.
Purpose of the Study:
- To review current advancements in prostate cancer therapeutics.
- To highlight novel drug molecules and targeted signaling pathways for combating metastatic and castration-resistant prostate cancer.
- To provide insights into emerging therapeutic strategies.
Main Methods:
- Review of scientific literature on prostate cancer diagnostics and therapeutics.
- Analysis of signaling pathways involved in prostate cancer growth, including AR and PI3K/AKT/mTOR.
- Evaluation of clinical trial data for novel therapeutic agents like PARP inhibitors and RISUG adv.
Main Results:
- Androgen deprivation therapy (ADT), often combined with abiraterone acetate or docetaxel, improves survival in metastatic hormone-sensitive prostate cancer (mHSPC).
- Poly ADP-ribose polymerase (PARP) inhibitors demonstrate efficacy in mCRPC patients with DNA repair defects.
- RISUG adv shows significant anti-prostate cancer activity in preclinical studies.
Conclusions:
- Targeting AR signaling, dihydrotestosterone production, and PI3K pathways is critical for effective prostate cancer treatment.
- Emerging therapies, including PARP inhibitors and RISUG adv, offer new hope for patients with advanced and resistant disease.
- Further research into novel drug molecules and targeted pathways is essential to overcome therapeutic challenges in prostate cancer.
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