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Role of stress in the pathogenesis of cancer (Review)

Stress is a state of disrupted homeostasis, triggered by intrinsic or extrinsic factors, the stressors, which are counteracted by various physiological and behavioural adaptive responses. Stress has been linked to cancer development and incidence for decades; however, epidemiological studies and cli...

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Autores principales: Lempesis, Ioannis G., Georgakopoulou, Vasiliki Epameinondas, Papalexis, Petros, Chrousos, Georgios P., Spandidos, Demetrios A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552722/
https://www.ncbi.nlm.nih.gov/pubmed/37711028
http://dx.doi.org/10.3892/ijo.2023.5572
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author Lempesis, Ioannis G.
Georgakopoulou, Vasiliki Epameinondas
Papalexis, Petros
Chrousos, Georgios P.
Spandidos, Demetrios A.
author_facet Lempesis, Ioannis G.
Georgakopoulou, Vasiliki Epameinondas
Papalexis, Petros
Chrousos, Georgios P.
Spandidos, Demetrios A.
author_sort Lempesis, Ioannis G.
collection PubMed
description Stress is a state of disrupted homeostasis, triggered by intrinsic or extrinsic factors, the stressors, which are counteracted by various physiological and behavioural adaptive responses. Stress has been linked to cancer development and incidence for decades; however, epidemiological studies and clinical trials have yielded contradictory results. The present review discusses the effects of stress on cancer development and the various underlying mechanisms. Animal studies have revealed a clear link between stress and cancer progression, revealing molecular, cellular and endocrine processes that are implicated in these effects. Thus, stress hormones, their receptor systems and their intracellular molecular pathways mediate the effects of stress on cancer initiation, progression and the development of metastases. The mechanisms linking stress and cancer progression can either be indirect, mediated by changes in the cancer microenvironment or immune system dysregulation, or direct, through the binding of neuroendocrine stress-related signalling molecules to cancer cell receptors. Stress affects numerous anti- and pro-cancer immune system components, including host resistance to metastasis, tumour retention and/or immune suppression. Chronic psychological stress through the elevation of catecholamine levels may increase cancer cell death resistance. On the whole, stress is linked to cancer development and incidence, with psychological stressors playing a crucial role. Animal studies have revealed a better link than human ones, with stress-related hormones influencing tumour development, migration, invasion and cell proliferation. Randomized controlled trials are required to further evaluate the long-term cancer outcomes of stress and its management.
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spelling pubmed-105527222023-10-06 Role of stress in the pathogenesis of cancer (Review) Lempesis, Ioannis G. Georgakopoulou, Vasiliki Epameinondas Papalexis, Petros Chrousos, Georgios P. Spandidos, Demetrios A. Int J Oncol Review Stress is a state of disrupted homeostasis, triggered by intrinsic or extrinsic factors, the stressors, which are counteracted by various physiological and behavioural adaptive responses. Stress has been linked to cancer development and incidence for decades; however, epidemiological studies and clinical trials have yielded contradictory results. The present review discusses the effects of stress on cancer development and the various underlying mechanisms. Animal studies have revealed a clear link between stress and cancer progression, revealing molecular, cellular and endocrine processes that are implicated in these effects. Thus, stress hormones, their receptor systems and their intracellular molecular pathways mediate the effects of stress on cancer initiation, progression and the development of metastases. The mechanisms linking stress and cancer progression can either be indirect, mediated by changes in the cancer microenvironment or immune system dysregulation, or direct, through the binding of neuroendocrine stress-related signalling molecules to cancer cell receptors. Stress affects numerous anti- and pro-cancer immune system components, including host resistance to metastasis, tumour retention and/or immune suppression. Chronic psychological stress through the elevation of catecholamine levels may increase cancer cell death resistance. On the whole, stress is linked to cancer development and incidence, with psychological stressors playing a crucial role. Animal studies have revealed a better link than human ones, with stress-related hormones influencing tumour development, migration, invasion and cell proliferation. Randomized controlled trials are required to further evaluate the long-term cancer outcomes of stress and its management. D.A. Spandidos 2023-09-11 /pmc/articles/PMC10552722/ /pubmed/37711028 http://dx.doi.org/10.3892/ijo.2023.5572 Text en Copyright: © Lempesis et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Lempesis, Ioannis G.
Georgakopoulou, Vasiliki Epameinondas
Papalexis, Petros
Chrousos, Georgios P.
Spandidos, Demetrios A.
Role of stress in the pathogenesis of cancer (Review)
title Role of stress in the pathogenesis of cancer (Review)
title_full Role of stress in the pathogenesis of cancer (Review)
title_fullStr Role of stress in the pathogenesis of cancer (Review)
title_full_unstemmed Role of stress in the pathogenesis of cancer (Review)
title_short Role of stress in the pathogenesis of cancer (Review)
title_sort role of stress in the pathogenesis of cancer (review)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552722/
https://www.ncbi.nlm.nih.gov/pubmed/37711028
http://dx.doi.org/10.3892/ijo.2023.5572
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