Related Experiment Video
Updated: Aug 6, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Antisense targets to enhance hormone and cytotoxic therapies in advanced prostate cancer
Martin Gleave1, Colleen Nelson, Kim Chi
1The Prostate Centre at Vancouver General Hospital, Division of Urology, University of British Columbia, D9, 2733 Heather Street, Vancouver, BC, Canada V6H 3Z3. gleave@interchange.ubc.ca
Abstract:
The main obstacle to improved survival of advanced prostate cancer is our failure to prevent or treat its progression to its lethal and untreatable stage of androgen independence. New therapeutic agents designed to prevent androgen-independent progression are required. Accelerated identification and characterization of cancer-relevant molecular targets has sparked considerable interest in the development of new generations of anti-cancer agents that specifically inhibit a progression-relevant target. Antisense oligonucleotides, short synthetic stretches of chemically modified DNA capable of specifically hybridizing to the mRNA of a chosen cancer-relevant target gene. promise to show enhanced specificity for malignant cells with a more favorable side-effect profile due to well-defined and tailored modes of action. Although not all of the challenges have been met to date, emerging clinical evidence supports the premise that antisense oligonucleotides stand a realistic chance of emerging as major partners of rationally designed anti-cancer regimens. The status of antisense targeting of several genes, including bcl-2, bcl-xL, clusterin, androgen receptor and IGFBPs, relevant to prostate and other cancers, are reviewed.
Insights
New antisense oligonucleotides offer targeted therapy for advanced prostate cancer, potentially preventing progression to androgen independence. This approach shows promise for improved cancer treatment regimens.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Advanced prostate cancer survival is limited by progression to androgen independence.
- Novel therapeutic agents are needed to prevent this lethal stage.
- Targeting cancer-specific molecular pathways is a key strategy for new anti-cancer drugs.
Purpose of the Study:
- To review the potential of antisense oligonucleotides as a new therapeutic strategy for advanced prostate cancer.
- To discuss the status of antisense targeting for key genes involved in prostate cancer progression.
Main Methods:
- Review of current literature on antisense oligonucleotide technology.
- Analysis of antisense targeting strategies for specific genes (bcl-2, bcl-xL, clusterin, androgen receptor, IGFBPs).
Main Results:
- Antisense oligonucleotides demonstrate high specificity for cancer cells.
- They offer a potentially favorable side-effect profile due to targeted action.
- Emerging clinical data suggest antisense oligonucleotides could be integral to future cancer therapies.
Conclusions:
- Antisense oligonucleotides represent a promising therapeutic modality for advanced prostate cancer.
- Targeting specific genes involved in androgen independence is a viable strategy.
- Further clinical development is warranted to realize the full potential of this approach.
Related Concept Videos
Protein Networks
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
siRNA - Small Interfering RNAs
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the ATP-dependent...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Transducer Mechanism: Enzyme-Linked Receptors
Major types that are helpful drug targets include:
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase

