Literature DB >> 11040271

The retinoids and cancer prevention mechanisms.

K H Dragnev1, J R Rigas, E Dmitrovsky.   

Abstract

Carcinogenesis is a multistep process that converts normal cells into malignant cells. Once transformed, malignant cells acquire the ability to invade and metastasize, leading to clinically evident disease. During this continuum from normal to metastatic cells, carcinogenic steps can be arrested or reversed through pharmacological treatments, known as cancer chemoprevention. Chemoprevention strategies represent therapeutic interventions at early stages of carcinogenesis, before the onset of invasive cancer. Effective chemoprevention should reduce or avoid the clinical consequences of overt malignancies by treating early neoplastic lesions before development of clinically apparent signs or symptoms. Preclinical, clinical, and epidemiological data provide considerable support for cancer chemoprevention as an attractive therapeutic strategy. This clinical approach was validated in the recent tamoxifen randomized trial, demonstrating that a selective estrogen receptor modulator reduces the risk of breast cancer in women at high risk for this malignancy. Derivatives of vitamin A, the retinoids, have reported activity in treating specific premalignant lesions and reducing incidence of second primary tumors in patients with prior head and neck, lung or liver cancers. Whether the retinoids will prevent primary cancers at these sites is not yet known. Notably, a carotenoid (beta-carotene) was shown as inactive in primary prevention of lung cancers in high-risk individuals. This underscores the need for relevant in vitro models to identify pathways signaling chemopreventive effects. These models should assess the activity of candidate chemoprevention agents before the conduct of large and costly prevention trials. An improved understanding of cancer prevention mechanisms should aid in the discovery of new therapeutic targets and chemoprevention agents. Ideally, these agents should have tolerable clinical toxicities suitable for chronic administration to individuals at high risk for developing primary or second cancers. This article reviews what is now known from clinical and preclinical studies about the retinoids as cancer prevention agents.

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Year:  2000        PMID: 11040271     DOI: 10.1634/theoncologist.5-5-361

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  19 in total

1.  Direct channeling of retinoic acid between cellular retinoic acid-binding protein II and retinoic acid receptor sensitizes mammary carcinoma cells to retinoic acid-induced growth arrest.

Authors:  Anuradha S Budhu; Noa Noy
Journal:  Mol Cell Biol       Date:  2002-04       Impact factor: 4.272

Review 2.  Lung cancer. 1: prevention of lung cancer.

Authors:  G E Goodman
Journal:  Thorax       Date:  2002-11       Impact factor: 9.139

3.  Synergistic effect of co-treatment with all-trans retinoic acid and 9-cis retinoic acid on human lung cancer cell line at molecular level.

Authors:  Esther Sathya Bama; V M Berlin Grace; Viswanathan Sundaram; Perinba Dansiha Jesubatham
Journal:  3 Biotech       Date:  2019-03-30       Impact factor: 2.406

Review 4.  From carrot to clinic: an overview of the retinoic acid signaling pathway.

Authors:  Maria Theodosiou; Vincent Laudet; Michael Schubert
Journal:  Cell Mol Life Sci       Date:  2010-02-07       Impact factor: 9.261

5.  Anti-tumor effects of a novel retinoic acid metabolism blocking agent VN/14-1 in the N-methyl-N-nitrosourea-induced rat mammary carcinoma model and its effects on the uterus.

Authors:  Paul E Goss; Shangle Qi; Haiqing Hu; Lalji K Gediya; Puranik Purushottamachar; Abhijit M Godbole; Vincent C O Njar
Journal:  Breast Cancer Res Treat       Date:  2011-08-14       Impact factor: 4.872

6.  Structure and promoter characterization of aldo-keto reductase family 1 B10 gene.

Authors:  Ziwen Liu; Linlin Zhong; Paulette A Krishack; Sarah Robbins; Julia X Cao; Yupei Zhao; Stephen Chung; Deliang Cao
Journal:  Gene       Date:  2009-02-21       Impact factor: 3.688

7.  Retinoids induced astrocytic differentiation with down regulation of telomerase activity and enhanced sensitivity to taxol for apoptosis in human glioblastoma T98G and U87MG cells.

Authors:  Arabinda Das; Naren L Banik; Swapan K Ray
Journal:  J Neurooncol       Date:  2007-11-07       Impact factor: 4.130

8.  Aldo-keto reductase family 1 member B10 promotes cell survival by regulating lipid synthesis and eliminating carbonyls.

Authors:  Chun Wang; Ruilan Yan; Dixian Luo; Kounosuke Watabe; Duan-Fang Liao; Deliang Cao
Journal:  J Biol Chem       Date:  2009-07-30       Impact factor: 5.157

9.  Retinoids activate RXR/CAR-mediated pathway and induce CYP3A.

Authors:  Shiyong Chen; Kun Wang; Yu-Jui Yvonne Wan
Journal:  Biochem Pharmacol       Date:  2009-08-15       Impact factor: 5.858

Review 10.  Retinoic acid actions through mammalian nuclear receptors.

Authors:  Pengxiang Huang; Vikas Chandra; Fraydoon Rastinejad
Journal:  Chem Rev       Date:  2013-12-05       Impact factor: 60.622

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