Literature DB >> 12549770

Chemoprevention of colon cancer: current status and future prospects.

David M Gustin1, Dean E Brenner.   

Abstract

Colorectal cancer is an important public health problem in the western world. Although some progress has been made in the prevention and management of this disease, colon cancer still remains one of the most common types of epithelial malignancies in both genders and is essentially incurable when it reaches the most advanced stages. Given the substantial morbidity and mortality associated with colorectal malignancies and their treatment, cancer prevention in its many forms emerges as a very attractive approach. Colorectal cancer chemoprevention refers to the administration of natural or synthetic compounds to block, reverse, delay or prevent the development of invasive large bowel neoplasms. The ultimate goal of implementing a chemopreventive intervention in the general, or alternatively, in an at-risk population is to decrease the incidence rate of the specific cancer being targeted. This article reviews the present status of colorectal cancer chemoprevention. Current insights into the molecular and genetic models of human colorectal carcinogenesis, preclinical models for efficacy testing as well as into promising biomarkers for colorectal chemoprevention are provided. The developmental status of many promising agents is also discussed emphasizing the epidemiological evidence, preclinical information substantiating an anticarcinogenic effect, their postulated mechanism of action and the status of human clinical development. Our perspective of the future prospects in this scientific area is also provided and has been predicated primarily on the firm belief that the proper integration of advances in the biology of colon carcinogenesis, experimental therapeutics and clinical trial methodology will be critical for the success of this promising field.

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Year:  2002        PMID: 12549770     DOI: 10.1023/a:1021271229476

Source DB:  PubMed          Journal:  Cancer Metastasis Rev        ISSN: 0167-7659            Impact factor:   9.264


  17 in total

1.  Programmed cell death factor 4 enhances the chemosensitivity of colorectal cancer cells to Taxol.

Authors:  Daqing Wang; Qianqian Hou; Lingjun Zhao; Jun Gao; Yang Xiao; Anhua Wang
Journal:  Oncol Lett       Date:  2019-05-27       Impact factor: 2.967

2.  Natural products and colon cancer: current status and future prospects.

Authors:  Subapriya Rajamanickam; Rajesh Agarwal
Journal:  Drug Dev Res       Date:  2008-11-01       Impact factor: 4.360

3.  Nitric oxide-donating aspirin inhibits beta-catenin/T cell factor (TCF) signaling in SW480 colon cancer cells by disrupting the nuclear beta-catenin-TCF association.

Authors:  Niharika Nath; Khosrow Kashfi; Jie Chen; Basil Rigas
Journal:  Proc Natl Acad Sci U S A       Date:  2003-10-17       Impact factor: 11.205

4.  Pien Tze Huang inhibits the proliferation of human colon carcinoma cells by arresting G1/S cell cycle progression.

Authors:  Aling Shen; Fei Hong; Liya Liu; Jiumao Lin; Lihui Wei; Qiaoyan Cai; Zhenfeng Hong; Jun Peng
Journal:  Oncol Lett       Date:  2012-07-19       Impact factor: 2.967

5.  Berberine, a natural isoquinoline alkaloid, induces NAG-1 and ATF3 expression in human colorectal cancer cells.

Authors:  Rojsanga Piyanuch; Mugdha Sukhthankar; Gritsanapan Wandee; Seung Joon Baek
Journal:  Cancer Lett       Date:  2007-10-25       Impact factor: 8.679

6.  NO-donating aspirin inhibits the activation of NF-kappaB in human cancer cell lines and Min mice.

Authors:  Jennie L Williams; Ping Ji; Nengtai Ouyang; Xiaoping Liu; Basil Rigas
Journal:  Carcinogenesis       Date:  2008-01-03       Impact factor: 4.944

Review 7.  Meta-analysis of different test indicators: Helicobacter pylori infection and the risk of colorectal cancer.

Authors:  Ya-Shuang Zhao; Fan Wang; Dong Chang; Bing Han; Ding-Yun You
Journal:  Int J Colorectal Dis       Date:  2008-05-28       Impact factor: 2.571

8.  AMP-activated protein kinase (AMPK)/Ulk1-dependent autophagic pathway contributes to C6 ceramide-induced cytotoxic effects in cultured colorectal cancer HT-29 cells.

Authors:  Hai-zhong Huo; Bing Wang; Jian Qin; Shan-yu Guo; Wen-yong Liu; Yan Gu
Journal:  Mol Cell Biochem       Date:  2013-03-19       Impact factor: 3.396

9.  Hedyotis diffusa willd extract suppresses colorectal cancer growth through multiple cellular pathways.

Authors:  Jianyu Feng; Yiyi Jin; Jun Peng; Lihui Wei; Qiaoyan Cai; Zhaokun Yan; Zijun Lai; Jiumao Lin
Journal:  Oncol Lett       Date:  2017-10-20       Impact factor: 2.967

10.  Hedyotis diffusa Willd extract inhibits HT-29 cell proliferation via cell cycle arrest.

Authors:  Minghe Lin; Jiumao Lin; Lihui Wei; Wei Xu; Zhenfeng Hong; Qiaoyan Cai; Jun Peng; Dezeng Zhu
Journal:  Exp Ther Med       Date:  2012-06-06       Impact factor: 2.447

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