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Chemoprevention of Lung Cancer: Prospects and Disappointments in Human Clinical Trials

Decreasing the risk of lung cancer, or preventing its development in high-risk individuals, would have a huge impact on public health. The most effective means to decrease lung cancer incidence is to eliminate exposure to carcinogens. However, with recent advances in the understanding of pulmonary c...

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Autores principales: Greenberg, Alissa K., Tsay, Jun-Chieh, Tchou-Wong, Kam-Meng, Jorgensen, Anna, Rom, William N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3730305/
https://www.ncbi.nlm.nih.gov/pubmed/24216701
http://dx.doi.org/10.3390/cancers5010131
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author Greenberg, Alissa K.
Tsay, Jun-Chieh
Tchou-Wong, Kam-Meng
Jorgensen, Anna
Rom, William N.
author_facet Greenberg, Alissa K.
Tsay, Jun-Chieh
Tchou-Wong, Kam-Meng
Jorgensen, Anna
Rom, William N.
author_sort Greenberg, Alissa K.
collection PubMed
description Decreasing the risk of lung cancer, or preventing its development in high-risk individuals, would have a huge impact on public health. The most effective means to decrease lung cancer incidence is to eliminate exposure to carcinogens. However, with recent advances in the understanding of pulmonary carcinogenesis and the identification of intermediate biomarkers, the prospects for the field of chemoprevention research have improved dramatically. Here we review the most recent research in lung cancer chemoprevention—focusing on those agents that have been investigated in human clinical trials. These agents fall into three major categories. First, oxidative stress plays an important role in pulmonary carcinogenesis; and therefore, antioxidants (including vitamins, selenium, green tea extracts, and isothiocyanates) may be particularly effective in preventing the development of lung cancer. Second, inflammation is increasingly accepted as a crucial factor in carcinogenesis, and many investigators have focused on anti-inflammatory agents, such as glucocorticoids, NSAIDs, statins, and PPARγ agonists. Finally, the PI3K/AKT/mTOR pathway is recognized to play a central role in tobacco-induced carcinogenesis, and inhibitors of this pathway, including myoinositol and metformin, are promising agents for lung cancer prevention. Successful chemoprevention will likely require targeting of multiple pathways to carcinogenesis—both to minimize toxicity and maximize efficacy.
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spelling pubmed-37303052013-08-05 Chemoprevention of Lung Cancer: Prospects and Disappointments in Human Clinical Trials Greenberg, Alissa K. Tsay, Jun-Chieh Tchou-Wong, Kam-Meng Jorgensen, Anna Rom, William N. Cancers (Basel) Review Decreasing the risk of lung cancer, or preventing its development in high-risk individuals, would have a huge impact on public health. The most effective means to decrease lung cancer incidence is to eliminate exposure to carcinogens. However, with recent advances in the understanding of pulmonary carcinogenesis and the identification of intermediate biomarkers, the prospects for the field of chemoprevention research have improved dramatically. Here we review the most recent research in lung cancer chemoprevention—focusing on those agents that have been investigated in human clinical trials. These agents fall into three major categories. First, oxidative stress plays an important role in pulmonary carcinogenesis; and therefore, antioxidants (including vitamins, selenium, green tea extracts, and isothiocyanates) may be particularly effective in preventing the development of lung cancer. Second, inflammation is increasingly accepted as a crucial factor in carcinogenesis, and many investigators have focused on anti-inflammatory agents, such as glucocorticoids, NSAIDs, statins, and PPARγ agonists. Finally, the PI3K/AKT/mTOR pathway is recognized to play a central role in tobacco-induced carcinogenesis, and inhibitors of this pathway, including myoinositol and metformin, are promising agents for lung cancer prevention. Successful chemoprevention will likely require targeting of multiple pathways to carcinogenesis—both to minimize toxicity and maximize efficacy. MDPI 2013-01-24 /pmc/articles/PMC3730305/ /pubmed/24216701 http://dx.doi.org/10.3390/cancers5010131 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Greenberg, Alissa K.
Tsay, Jun-Chieh
Tchou-Wong, Kam-Meng
Jorgensen, Anna
Rom, William N.
Chemoprevention of Lung Cancer: Prospects and Disappointments in Human Clinical Trials
title Chemoprevention of Lung Cancer: Prospects and Disappointments in Human Clinical Trials
title_full Chemoprevention of Lung Cancer: Prospects and Disappointments in Human Clinical Trials
title_fullStr Chemoprevention of Lung Cancer: Prospects and Disappointments in Human Clinical Trials
title_full_unstemmed Chemoprevention of Lung Cancer: Prospects and Disappointments in Human Clinical Trials
title_short Chemoprevention of Lung Cancer: Prospects and Disappointments in Human Clinical Trials
title_sort chemoprevention of lung cancer: prospects and disappointments in human clinical trials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3730305/
https://www.ncbi.nlm.nih.gov/pubmed/24216701
http://dx.doi.org/10.3390/cancers5010131
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