Biobehavioral factors and cancer progression: physiological pathways and mechanisms - PubMed (original) (raw)
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Biobehavioral factors and cancer progression: physiological pathways and mechanisms
Susan K Lutgendorf et al. Psychosom Med. 2011 Nov-Dec.
Abstract
Epidemiologic evidence increasingly has supported the role of biobehavioral risk factors such as social adversity, depression, and stress in cancer progression. This review describes in vitro, in vivo, and clinical studies demonstrating relationships between such processes and pathways involved in cancer progression. These include effects on the cellular immune response, angiogenesis, invasion, anoikis, and inflammation. Biobehavioral factors have been shown to contribute to the cross talk between tumor and host cells in the tumor microenvironment, and stress effects on host cells such as macrophages seem to be critical for many pathways involved in tumor progression. Some effects are bidirectional in that tumor-derived inflammation seems to affect central nervous system processes, giving rise to vegetative symptoms and contributing to dysregulation of the hypothalamic-pituitary-adrenal axis with downstream effects on inflammatory control. Findings to date are reviewed, and fruitful areas for future research are discussed.
Figures
Figure 1
Effects of stress and psychosocial processes on the tumor microenvironment. The stress response results in activation of the autonomic nervous system and the hypothalamic-pituitary adrenal axis. Factors released from these pathways can have direct effects on the tumor microenvironment, resulting in a favorable environment for tumor growth and progression. These dynamics can also adversely affect patient quality of life. CRH, corticotropin releasing hormone; ACTH, adrenocorticotrophic hormone; NK natural killer; T-regs, regulatory T-cells; TAM, tumor associated macrophages; MMP, matrix metalloprotinease; VEGF, vascular endothelial growth factor; IL, interleukin; STAT3, signal transducer and activator of transcription factor-3; QOL, quality of life. Reprinted with permission. © 2008 American Society of Clinical Oncology. All rights reserved. Lutgendorf S., et al. J Clin Oncology, 28 (26) 2010, 4094-9.
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