Related Experiment Video
Updated: Jun 25, 2026

Development and Maintenance of a Preclinical Patient Derived Tumor Xenograft Model for the Investigation of Novel Anti-Cancer Therapies
Published on: September 30, 2016
Chemoprevention of colorectal cancer-experimental and clinical aspects-
Tetsuji Takayama1, Takahiro Goji, Tatsuya Taniguchi
1Department of Gastroenterology and Oncology, Institutes of Health Bioscience, the University of Tokushima Graduate School, Japan.
Abstract:
Colorectal cancer is a leading cause of cancer-related mortality worldwide. Therefore, an appropriate prevention strategy should be urgently established. Chemoprevention involves the use of oral agents to suppress the development of cancer. Recent progress in the molecular analysis of colorectal cancer has revealed many candidate molecules for chemoprevention. Many new agents targeting these molecules have also been developed. These agents are largely classified into three categories: 1) Signal transduction modulators including epidermal growth factor (EGF) receptor inhibitors, anti-vascular endothelial growth factor (VEGF) antibodies, and inhibitors of oncogene products. 2) Epigenetic modulators including peroxisome proliferative activated receptor (PPAR)-gamma agonists, estrogen receptor (ER)-beta, and histone deacetylase inhibitors. 3) Anti-inflammatory modulators including cyclooxygenase (COX)-2, EP 1-4, and NF-kB. Of these agents, some actually proceeded to human clinical trials, and have been shown to be active chemopreventive agents.
Insights
Chemoprevention uses oral agents to prevent colorectal cancer development. New targeted agents, including signal transduction, epigenetic, and anti-inflammatory modulators, show promise in clinical trials for cancer prevention.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Colorectal cancer is a major global cause of cancer mortality.
- Effective prevention strategies are urgently needed.
- Chemoprevention, using oral agents, offers a promising approach to suppress cancer development.
Purpose of the Study:
- To review recent advances in colorectal cancer chemoprevention.
- To categorize novel chemopreventive agents based on their molecular targets.
- To highlight agents that have progressed to human clinical trials.
Main Methods:
- Review of molecular analyses of colorectal cancer.
- Classification of chemopreventive agents into three main categories: signal transduction modulators, epigenetic modulators, and anti-inflammatory modulators.
- Examination of agents targeting specific molecules like epidermal growth factor (EGF) receptor, vascular endothelial growth factor (VEGF), peroxisome proliferative activated receptor (PPAR)-gamma, estrogen receptor (ER)-beta, histone deacetylase, cyclooxygenase (COX)-2, and NF-kB.
Main Results:
- Identification of numerous candidate molecules for colorectal cancer chemoprevention.
- Development of new agents targeting these molecules, categorized as signal transduction, epigenetic, or anti-inflammatory modulators.
- Successful progression of some agents into human clinical trials, demonstrating chemopreventive activity.
Conclusions:
- Targeted chemoprevention represents a significant advancement in colorectal cancer prevention.
- Various classes of novel agents show potential for clinical application.
- Further research and clinical trials are warranted to optimize these strategies for reducing colorectal cancer mortality.
More Related Videos
06:24Establishment of Coloproctitis Cancer Model in Mice and Evaluation of Therapeutic Effect of Chinese Medicine
Published on: October 13, 2023
09:01Non-invasive Assessment of the Efficacy of New Therapeutics for Intestinal Pathologies Using Serial Endoscopic Imaging of Live Mice
Published on: March 10, 2015
Related Concept Videos
Cancer Prevention
Some...
Cancer Prevention
Some...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...