Impact of Neuro-Psychological Factors on Smoking-Associated Lung Cancer

Smoking has been extensively documented as a risk factor for all histological types of lung cancer and tobacco-specific nitrosamines and polycyclic aromatic hydrocarbons reproducibly cause lung cancer in laboratory rodents. However, the most common lung cancer, non-small cell lung cancer (NSCLC), fr...

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Main Author: Hildegard M. Schuller
Format: Article
Language:English
Published: MDPI AG 2014-03-01
Series:Cancers
Subjects:
Online Access:http://www.mdpi.com/2072-6694/6/1/580
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spelling doaj-5dd3abaf10594420bfde2cfa9b374eef2020-11-24T23:41:44ZengMDPI AGCancers2072-66942014-03-016158059410.3390/cancers6010580cancers6010580Impact of Neuro-Psychological Factors on Smoking-Associated Lung CancerHildegard M. Schuller0Experimental Oncology Laboratory, Department of Biomedical and Diagnostic Sciences, College of Veterinary Medicine, University of Tennessee, 2407 River Drive, Knoxville, TN 37996, USASmoking has been extensively documented as a risk factor for all histological types of lung cancer and tobacco-specific nitrosamines and polycyclic aromatic hydrocarbons reproducibly cause lung cancer in laboratory rodents. However, the most common lung cancer, non-small cell lung cancer (NSCLC), frequently develops in never smokers and is particularly common in women and African Americans, suggesting that factors unrelated to smoking significantly impact this cancer. Recent experimental investigations in vitro and in animal models have shown that chronic psychological stress and the associated hyperactive signaling of stress neurotransmitters via β-adrenergic receptors significantly promote the growth and metastatic potential of NSCLC. These responses were caused by modulation in the expression and sensitization state of nicotinic acetylcholine receptors (nAChRs) that regulate the production of stress neurotransmitters and the inhibitory neurotransmitter γ-aminobutyric acid (GABA). Similar changes in nAChR-mediated neurotransmitter production were identified as the cause of NSCLC stimulation in vitro and in xenograft models by chronic nicotine. Collectively, these data suggest that hyperactivity of the sympathetic branch of the autonomic nervous system caused by chronic psychological stress or chronic exposure to nicotinic agonists in cigarette smoke significantly contribute to the development and progression of NSCLC. A recent clinical study that reported improved survival outcomes with the incidental use of β-blockers among patients with NSCLC supports this interpretation.http://www.mdpi.com/2072-6694/6/1/580smokingnon-small cell lung cancernicotinic receptorsb-adrenergic receptorssympathicus hyperactivitypsychological stress
collection DOAJ
language English
format Article
sources DOAJ
author Hildegard M. Schuller
spellingShingle Hildegard M. Schuller
Impact of Neuro-Psychological Factors on Smoking-Associated Lung Cancer
Cancers
smoking
non-small cell lung cancer
nicotinic receptors
b-adrenergic receptors
sympathicus hyperactivity
psychological stress
author_facet Hildegard M. Schuller
author_sort Hildegard M. Schuller
title Impact of Neuro-Psychological Factors on Smoking-Associated Lung Cancer
title_short Impact of Neuro-Psychological Factors on Smoking-Associated Lung Cancer
title_full Impact of Neuro-Psychological Factors on Smoking-Associated Lung Cancer
title_fullStr Impact of Neuro-Psychological Factors on Smoking-Associated Lung Cancer
title_full_unstemmed Impact of Neuro-Psychological Factors on Smoking-Associated Lung Cancer
title_sort impact of neuro-psychological factors on smoking-associated lung cancer
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2014-03-01
description Smoking has been extensively documented as a risk factor for all histological types of lung cancer and tobacco-specific nitrosamines and polycyclic aromatic hydrocarbons reproducibly cause lung cancer in laboratory rodents. However, the most common lung cancer, non-small cell lung cancer (NSCLC), frequently develops in never smokers and is particularly common in women and African Americans, suggesting that factors unrelated to smoking significantly impact this cancer. Recent experimental investigations in vitro and in animal models have shown that chronic psychological stress and the associated hyperactive signaling of stress neurotransmitters via β-adrenergic receptors significantly promote the growth and metastatic potential of NSCLC. These responses were caused by modulation in the expression and sensitization state of nicotinic acetylcholine receptors (nAChRs) that regulate the production of stress neurotransmitters and the inhibitory neurotransmitter γ-aminobutyric acid (GABA). Similar changes in nAChR-mediated neurotransmitter production were identified as the cause of NSCLC stimulation in vitro and in xenograft models by chronic nicotine. Collectively, these data suggest that hyperactivity of the sympathetic branch of the autonomic nervous system caused by chronic psychological stress or chronic exposure to nicotinic agonists in cigarette smoke significantly contribute to the development and progression of NSCLC. A recent clinical study that reported improved survival outcomes with the incidental use of β-blockers among patients with NSCLC supports this interpretation.
topic smoking
non-small cell lung cancer
nicotinic receptors
b-adrenergic receptors
sympathicus hyperactivity
psychological stress
url http://www.mdpi.com/2072-6694/6/1/580
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