Chronic Stress Promotes Cancer Development
- 1NHC Key Laboratory of Carcinogenesis and Hunan Key Laboratory of Translational Radiation Oncology, Hunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China
- 2Key Laboratory of Carcinogenesis and Cancer Invasion of the Chinese Ministry of Education, Cancer Research Institute, Central South University, Changsha, China
- 3Hunan Key Laboratory of Nonresolving Inflammation and Cancer, Disease Genome Research Center, The Third Xiangya Hospital, Central South University, Changsha, China
- 4Department of Medicine, Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, United States
Stress is an inevitable part of life. Chronic stress on account of reasons like adversity, depression, anxiety, or loneliness/social isolation can endanger human health. Recent studies have shown that chronic stress can induce tumorigenesis and promote cancer development. This review describes the latest progress of research on the molecular mechanisms by which chronic stress promotes cancer development. Primarily, chronic stress activates the classic neuroendocrine system [the hypothalamic-pituitary-adrenal (HPA) axis] and the sympathetic nervous system (SNS) and leads to a decline and dysfunction of the prefrontal cortex and the hippocampus under stress. Stress hormones produced during the activation of both the HPA axis and the SNS can promote tumorigenesis and cancer development through a variety of mechanisms. Chronic stress can also cause corresponding changes in the body's immune function and inflammatory response, which is significant because a long-term inflammatory response and the decline of the body's immune surveillance capabilities are implicated in tumorigenesis. Stress management is essential for both healthy people and cancer patients. Whether drugs that limit the signaling pathways downstream of the HPA axis or the SNS can suppress chronic stress-induced cancers or prolong patient survival deserves further study.
Humans have always experienced periods of excessive stress on account of global issues, such as poverty, war, and epidemics (1). Stress can be divided into acute stress and chronic stress. Acute stress usually exists in emergencies, such as fighting or escaping. Changes in the structure and function of certain molecules and tissues in the brain activate the emotional cognitive system, and we make decisions for stress-coping mechanisms (2). At the same time, the body temporarily produces catecholamines and corticosteroids to improve mobility and responsiveness. Therefore, acute stress is often beneficial to the body. However, chronic stress is heavily implicated in causing ill health, and today it is considered to encompass occupational stress as well as unusual adversities. Its potential negative effects include not only insomnia, gastrointestinal disorders (3, 4), anxiety, and depression (5, 6), but also an increased risk of cardiovascular disease, mental illness, and cancer (7).
Surveys have shown that approximately one million new cancer cases occur every year among young people aged 20–39 years (7), and they have been partly attributed to stress. The relationship between chronic stress and cancers has aroused increasingly widespread interest and concern in the medical community. Many scholars have performed research on the relationships between stress and cancers such as prostate (8–10), breast (8–12), gastric (13, 14), lung (15, 16), and skin cancer (17, 18), and have found evidence indicating that chronic stress can induce tumorigenesis and promote cancer development (Table 1).
The neuroendocrine pathways are the most widely and comprehensively studied possible mediators of these associations. The neuroendocrine pathways constituting the hypothalamus-pituitary-adrenal (HPA) axis and the sympathetic nervous system (SNS) were the first systems shown to be closely related to stress [(1, 19); Figure 1]. Under chronic stress, the brain's nerve impulses can continuously activate the hypothalamus to produce the corticotropin-releasing factor (CRF). CRF is transported through the blood to the pituitary gland, thereby stimulating cells to release the adrenocorticotropic hormone (ACTH), which travels through the blood to the adrenal cortex and promotes the synthesis of corticosteroids. Chronic stress also activates the SNS, thereby stimulating the release of important neurotransmitters such as norepinephrine (NA) and adrenaline (Ad). NA and Ad are also hormones secreted by the adrenal medulla and known as catecholamines because they contain catechol and amine groups. The corticosteroids and catecholamines produced by the HPA and the SNS can cause a decline in the functions of the prefrontal cortex (20) and the hippocampus (21), and may enhance the activation of the SNS and the HPA by regulating the expression of glucocorticoid receptors (5, 22, 23).
Figure 1. The neuroendocrine mechanisms of chronic stress. Chronic stress produces stress hormones during the activation of the neuroendocrine system (hypothalamus-pituitary-adrenal axis) and the sympathetic nervous system, which can promote tumor development and regulate the tumor microenvironment.
Stress hormones promote the occurrence and development of cancers through various mechanisms such as by inducing DNA damage, increasing p53 degradation, and regulating the tumor microenvironment (Figure 1). Chronic stress can also activate the inflammatory response and the interaction between inflammatory cells and cancer cells to form the inflammatory tumor microenvironment, thereby promoting all stages of tumorigenesis (24). It can also enhance neuroinflammation, which further impairs the brain's cognitive processing of stress. This is a vicious circle. Chronic stress can also selectively suppress the type 1 helper T cells (Th1), suppress the cytotoxic T cells (CTL)-mediated cellular immunity and interferon production, and weaken immune surveillance and other processes, thereby increasing the risk of cancer invasion and metastasis and reducing the effectiveness of anti-tumor therapy (25, 26). In summary, chronic stress can promote tumorigenesis and oncogenesis through the production of stress hormones, the activation of inflammation, and the suppression of immunity. Therefore, the present review has focused on these three stress-mediated activities.
Stress Hormones Promote Tumorigenesis and Cancer Development
Stress hormones are classified into classical corticosteroids and catecholamines, as well as the non-classical CRF and thyroid hormones.
Classical Corticosteroids and Catecholamines
Corticosteroids include glucocorticoids and corticosterones. Elevated glucocorticoid levels increase the activity of the negative regulator murine double minute 2 (MDM2) through induction of the serum-and-glucocorticoid-regulated kinase (SGK1) and mediate the inhibition of p53 (27). P53 can initiate DNA repair, cell cycle arrest, aging, and apoptosis, which are related to the body's ability to inhibit tumor formation and respond to various types of cancer treatment (28). Therefore, the loss or impairment of the p53 function mediated by corticosteroids can considerably promote tumorigenesis. Obradović et al. (29) found that the increase in glucocorticoids during breast cancer progression was related to a lower survival rate. Increased hormone levels could lead to the activation of glucocorticoid receptors that were involved in the activation of multiple processes in metastasis and the up-regulation of kinase orphan receptor 1 (ROR1) at distant metastatic sites. Inhibition of ROR1 expression can reduce metastasis and prolong the survival rates of breast cancer patients.
Catecholamines can regulate the tumor microenvironment (30). In prostate cancer, catecholamines in the local sympathetic nerve fibers (NA) and circulating blood (Ad) can activate the β-adrenergic receptors (βARs) on endothelial cells, altering the cell metabolism, thereby inhibiting their oxidative phosphorylation, and inducing angiogenesis (31, 32). They can also activate the βARs in pancreatic cancer and stromal cells to increase the expression of invasive genes, thereby promoting the growth of primary tumors and the spread of tumor cells to adjacent tissues (33).
The tumor-promoting effect of catecholamines is mainly mediated by the β2 adrenergic receptor (encoded by ADRB2) activating the cAMP-protein kinase A (PKA) signaling pathway, which is the main mechanism to enhance tumor angiogenesis in the body and promote the growth of malignant cells [(34, 35); Figure 2]. The downstream mechanisms include mediating Src phosphorylation, DNA damage, p53 degradation, and the up-regulation of vascular endothelial growth factor (VEGF) and matrix metalloproteinases (MMP-2 and MMP-9). Catecholamines also mediate Src phosphorylation via βARs-cAMP-PKA, activate Ras-related protein 1 (Rap1), and inhibit extracellular signal-regulated kinases (ERKs), thereby enhancing tumor cell migration, invasion, and growth (36). Src is a non-receptor cytosolic tyrosine kinase that is involved in the VEGF and interleukin (IL-6) production in adipocytes and cancer cells, respectively (37).
Figure 2. Signaling pathways activated by catecholamines. Stress-induced catecholamines activate the cAMP-PKA signaling pathway through β2 adrenergic receptors, thereby causing a series of downstream reactions. Src phosphorylation, DNA damage, p53 degradation, upregulation of VEGF and MMPs, and enhanced stem-like traits are key factors of tumorigenesis.
Hara's team (38) clarified the specific mechanism of stress-mediated DNA damage. Catecholamines can stimulate the G-proteins (Gs)-PKA-mediated signaling pathways to trigger DNA damage and the β-arrestin (ARRB1)-mediated signaling pathways to trigger the Akt-mediated activation of MDM2, which promotes the binding and degradation of MDM2 and p53 by binding to M53. The synergy of these two pathways leads to the accumulation of DNA damage.
Angiogenesis is an important part of tumor development and metastasis. Studies have found significantly increased tumor blood vessel formation in stressed animals, and the mechanism maybe a βARs-cAMP-PKA-IL-6-dependent activation of signal transduction and activator of transcription (STAT3) (39). Activated STAT3 is transported to the nucleus and binds to specific DNA sites in the form of homo- or heterodimers, stimulating the transcription of the reactive genes VEGF, MMP2, and MMP9 (34). VEGF plays a central role in the pathogenesis of various cancers as the best-known angiogenesis stimulator (40). When combined with its VEGF receptors on vascular endothelial cells, VEGF can promote tumor neovascularization. MMPs can degrade multiple protein components in the extracellular matrix, destroy the histological barrier of tumor cell invasion, and play a key role in tumor invasion and metastasis.
Cui et al. (8) found that chronic stress could induce adrenaline to activate lactate dehydrogenase A (LDHA) to produce lactic acid. The adjusted pH is conducive to the ubiquitin-specific protease 28 (USP28)-mediated ubiquitination and stabilization of MYC, and MYUG activates the SLUG promoter, which promotes the development of stem-like traits in breast cancer. Jang et al. (16) demonstrated that NA could induce the phosphorylation of the L-type voltage-dependent calcium channels (VDCC) via theβAR-PKA pathway. They further found that VDCC could trigger calcium mobilization, thereby inducing the activation of the insulin-like growth factor receptor (IGF-1R) and promoting cancer metastasis through the exocytosis of IGF2.
Motivated by studies of this mechanism, many researchers have tried to reverse the occurrence of the cancer-promoting effects by blocking the β2-AR and its downstream signaling pathway (Figure 2). Zhang et al. (41) found that by blocking the β2-ARs, a G1/S phase arrest and apoptosis could be induced in pancreatic cancer cells via the Ras/Akt/NFκB pathway. Hassan et al. (42) demonstrated an interaction between prostate cancers and the socio-psychological environment mediated by activating the Ad/ADRB2/PKA/BAD anti-apoptotic signaling pathway. They used the selective ADRB2 antagonist ICI118,551, or induced expression of the PKA inhibitor (PKI) or the BCL2-related death promoter BAD (BADS112A) with a mutated PKA phosphorylation site, to prevent the effects of stress in xenograft cancers. ADRB2 antagonists such as propranolol and ICI118,551 suppressed gastric cancer progression by inhibiting the ERK1/2-JNK-MAPK pathway and transcription factors, such as NF-κB, AP-1, and STAT3 (14). Cui et al. (8) conducted drug screening for LDHA and found that vitamin C could reverse the stem-like phenotype of breast cancer induced by chronic stress. Therefore, vitamin C may be a potential factor to combat stress-related breast cancer.
CRF and Thyroid Hormone
CRF is widely present in the central nervous system, that has been detected in breast cancer tissues and cell lines, and affects breast cancer cell proliferation and invasion in an autocrine or paracrine manner (10). CRF can induce the phosphorylation of the focal adhesion kinase (FAK), induce Cox1 to produce prostaglandins, directly promote actin recombination and cell migration, and play a role in the TGFβ/SMAD2 and the Wnt-β-catenin signaling. The antagonist of CRF, antalarmin, inhibits neovascularization in 4T1 breast cancer cell lines in vivo (43).
Thyroid hormone is secreted by the thyroid gland, which is closely related to the body's metabolism, growth, and development, and is regulated by the hypothalamus-pituitary-thyroid axis. When people are emotional, their emotions stimulate the hypothalamus to release thyrotropin-releasing hormones and regulate the secretion of thyroid-stimulating hormones. This further affects the thyroid gland, and causes its gland cells to secrete a large amount of thyroid hormone. Frick et al. (44) found that under chronic stress, thyroid hormone levels and T cell lymphoid tissue hyperplasia response were reduced in animals and lymphoma growth was altered. The use of thyroxine replacement therapy can reverse the above process. Therefore, thyroid hormone may be a critical neuroendocrine regulator of tumor evolution, most likely through the regulation of T cell-mediated immunity.
Chronic Stress Enhances Inflammation to Promote Tumor Development
Chronic stress and stress hormones can up-regulate the expression of stress-related pro-inflammatory genes in the circulating white blood cells, thereby increasing the release of pro-inflammatory cells and the production of pro-inflammatory cytokines, and can activate the aging-inflammatory response without the trigger of an exogenous inflammation, leading to the promotion of tumorigenesis and metastasis (45). Niraula et al. (46) found that high levels of corticosterone under repeated pressures of social failure promoted the release of the bone marrow-derived proinflammatory monocytes into the circulatory system and circulated in the brain, increasing neuroinflammation, and leading to a prolonged anxiety-like behavior. Inhibiting corticosterone overproduction through surgery (adrenalectomy) and drug therapy (metyrapone) can reduce these inflammatory responses to stress. Pretreatment of the socially disruptive-stressed mice with the β-adrenergic antagonist propranolol may prevent anxiety-like behaviors caused by social failure (47), reverse splenomegaly, and increase the levels of plasma inflammatory factors such as IL-6, tumor necrosis factor alpha (TNF-α), and the monocyte chemotactic protein 1 (MCP-1) (48). Moreover, research by Antoni's group shows that stress management in patients with early-stage breast cancer can reverse the up-regulation of the stress-related proinflammatory genes in white blood cells in the circulation (49).
Immune cells in the tumor microenvironment are called pro-tumorigenic immune cells and include the tumor-associated macrophages (TAMs), the dendritic cells (DCs), the myeloid-derived suppressor cells (MDSCs), and the tumor-infiltrating lymphocytes (TILs). These immune cells can produce cytokines such as IL-6, IL-10, TNF-α, and MCP-1, and are interconnected with tumor cells in an autocrine and paracrine manner. The pro-tumorigenic immune cells maintain a relative balance within a certain range of promoting tumor inflammation and anti-tumor immunity. After chronic stress breaks this balance through a long-term pro-inflammatory response, these cells and cytokines can act on all stages of tumor development, including initiation, promotion, malignant transformation, invasion, and metastasis through mutation, epigenetic modification, and regulation of the tumor microenvironment [(50, 51); Figure 3]. Moreover, activated inflammatory cells produce excess reactive oxygen species (ROS) to drive inflammation and mutagenesis through different pathways (52). The released cytokines can activate key transcription factors such as NF-κB (53–55) and STAT3 (56) in precancerous cells. By regulating the expression of many genes that can inhibit tumor cell death, promote tumor cell survival, and induce the production of chemokines, cytokines also attract more tumor-promoting immune cells to maintain a tumor-related inflammation.
Figure 3. Effects of stress hormones on the immune system. Stress hormones stimulate pro-tumorigenic immune cells to produce IL-6, IL-10, and other cytokines, and activate the COX-2/PGE2 pathway to produce VEGF, which together affect the tumor microenvironment to suppress tumor immunity. The decrease in IL-12 and the increase in IL-10 lead to selective Th1 inhibition, thereby suppressing the CTL-mediated cellular immunity and interferon production.
Chronic Stress Promotes Tumorigenesis and Cancer Development by Suppressing Immunity
As the core immune cells, thymus-dependent lymphocytes (T cells) provide a robust line of defense against infections and cancers. The cellular immunity mediated by them includes specific binding to their target cells for direct cell destruction or elimination and the release of cytokines to enhance and expand the immune effects. T cells can be roughly classified into the cytotoxic T cells, the helper T cells, and the regulatory/inhibitory T cells according to their functions. Based on different cytokine functions, the helper T cells are divided into Th1 or Th2 cells, which are differentiated from TH0 cells by their regulation by the cytokines IL-12 and IL-4. Th1 cells usually produce IFN-γ, TNF-β, and IL-2, and mediate cellular immune responses, such as inducing macrophage activation, mediating delayed hypersensitivity, and assisting CTL activation and proliferation. Th2 cells usually produces IL-4, IL-5, IL-6, and IL-10. Their main function is to enhance the humoral immune response and stimulate the B cells to produce antibodies. Notably, IL-12 and TNF-β promote a Th1 response and cellular immunity, while IL-10 inhibits IL-12 production and Th1 response and stimulates Th2 response and the humoral immunity (Figure 3).
Stress tests show that the plasma concentration of stress hormones is inversely proportional to the function of immune cells (57). Increased stress hormone production significantly reduces the activity of the antigen-presenting cells (APC), such as monocytes, macrophages, the dendritic cells, and the natural killer cells, that produce human IL-12 (58). Therefore, neuroendocrine mediators such as the stress-releasing glucocorticoids and epinephrine may selectively inhibit Th1, thereby inhibiting the CTL-mediated immune response and the production of interferon IFN-γ (26). Yang et al. (25) further confirmed that high levels of corticosteroids in plasma, and the up-regulated glucocorticoid-inducing factor Tsc22d3, blocked the activation of type I IFN response in DCs and IFN-γ+ T cells and reduced the efficacy of anti-tumor therapies in non-small cell lung cancer and colorectal cancer by suppressing the immune surveillance. Additionally, Saul et al. (17) found that chronic stress increased the sensitivity to the UV-induced squamous cell carcinoma by suppressing CTL and increasing the number of the regulatory/inhibitory T cells (Figure 3).
Stress hormones also induce cyclooxygenase COX-2 and a variety of COX-2-dependent inhibitors in human breast and colon cancer tissue cells, thereby activating the COX-2/PGE2 pathway (59). PGE2 is a biologically active lipid that can trigger inflammation and cancer. The activation of COX-2/PGE2 can affect the tumor microenvironment and inhibit tumor immunity through a variety of mechanisms, including inducing tumor cells to produce vascular endothelial growth factor C (VEGFC) and promoting the remodeling of lymphatic networks in and around tumors to provide a pathway for the tumor cells to escape the immune system [(60); Figure 3].
Conclusions and Future Perspectives
Chronic stress can activate the HPA axis, and the SNS, and cause immune disorders and inflammatory responses. There is no doubt that this is harmful to the body. Excessive levels of stress hormones promote carcinogenesis by inducing DNA damage accumulation, increasing p53 degradation, and other, related pathways. Excessive stress hormones also prevent immune cells from effectively controlling cancer cells by increasing inflammation and suppressing immunity. Further, they can act on tumor and stromal cells in the tumor microenvironment to promote tumor growth, invasion, and metastasis. In addition to these pathways, emerging trends include investigation of the correlation between chronic stress and the microbiota-gut-brain axis (61–63), and its impact on intestinal diseases (64).
The effects of daily stress on the neuroendocrine and immune function of healthy human individuals, which may be modulated by the individual's personality, have been confirmed, for example, by Biondi et al. (65). Therefore, we need to actively manage stress (66, 67). A large amount of clinical evidence shows that supportive psychological therapy has a positive effect on anticancer treatment and prognosis of cancer patients (68, 69). In addition to increasing exercise (70) and psychological intervention (71–74) to regulate the patients' stress, we can also use drugs that limit the transmission of the HPA axis and the downstream signaling pathways of the SNS, such as the β-adrenergic receptor antagonists [(9); Figure 2], COX2 inhibitors (COX2i) [(59, 75); Figure 3], anti-VEGFC therapeutics (αVEGFC) or dopamine (76) (an inhibitory catecholamine). These drugs have been shown in animal experiments to not only significantly improve anxiety-like behavior (47, 48), and inhibit chronic tumor-promoting tumor growth, but also to block a stress-induced increase in angiogenesis and lymphatic metastasis (60). At the same time, we suggest that stress hormones should be used with caution, especially glucocorticoids (77) to treat patients with cancer and related complications. Finally, it is notable that β-blockers have been relatively widely used in clinical research (78, 79) and are often administered as adjuvants in cancer treatment in recent years [(80–84); Table 2], especially in breast cancer treatment. Though other related drugs have shown promise for treating cancer, there remains insufficient evidence for their clinical application.
SD, YM, and YW collected the related paper and finished the manuscript, tables, and figures. YL, WX, GL, CG, and ZZ gave constructive guidance and made critical revisions. BX, QL, MZ, and XL participated in the design of this review. All authors read and approved the final manuscript.
This work was supported partially by grants from the National Natural Science Foundation of China (81972776, 81872278, 81772928, 81702907, and 81672683) and the Natural Science Foundation of Hunan Province (2018SK21210, 2018SK21211, 2018JJ3704, and 2017SK2105).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
AR, adrenergic receptor; ACTH, adrenocorticotropic hormone; Ad, adrenaline; APC, antigen-presenting cell; ARRB1, β-arrestin; CRF, corticotropin releasing factor; DC, dendritic cell; FAK, focal adhesion kinase; HPA, hypothalamic-pituitary-adrenal; IGF-1R, insulin-like growth factor receptor; IL, interleukin; LDHA, lactate dehydrogenase A; MCP-1, monocyte chemotactic protein 1; MDM2, negative regulator murine double minute 2; MDSC, myeloid-derived suppressor cell; MMPs, matrix metalloproteinases; NA, norepinephrine; PKA, cAMP-protein kinase A; ROR1, receptor tyrosine kinase-like orphan receptor 1; ROS, reactive oxygen species; SGK1, serum-and-glucocorticoid-regulated kinase; SNS, sympathetic nervous system; STAT3, signal transduction and activator of transcription; T cell, thymus-dependent lymphocyte; TAM, tumor-associated macrophage; Th1, type 1 helper T cell; TIL, tumor-infiltrating lymphocyte; TNF-α, tumor necrosis factor alpha; VDCC, voltage-dependent calcium channel; VEGF, vascular endothelial growth factor.
3. Alonso C, Guilarte M, Vicario M, Ramos L, Ramadan Z, Antolin M, et al. Maladaptive intestinal epithelial responses to life stress may predispose healthy women to gut mucosal inflammation. Gastroenterology. (2008) 135:163–72.e1. doi: 10.1053/j.gastro.2008.03.036
5. Zhou QG, Zhu LJ, Chen C, Wu HY, Luo CX, Chang L, et al. Hippocampal neuronal nitric oxide synthase mediates the stress-related depressive behaviors of glucocorticoids by downregulating glucocorticoid receptor. J Neurosci. (2011) 31:7579–90. doi: 10.1523/JNEUROSCI.0004-11.2011
7. Fidler MM, Gupta S, Soerjomataram I, Ferlay J, Steliarova-Foucher E, Bray F. Cancer incidence and mortality among young adults aged 20-39 years worldwide in 2012: a population-based study. Lancet Oncol. (2017) 18:1579–89. doi: 10.1016/S1470-2045(17)30677-0
8. Cui B, Luo Y, Tian P, Peng F, Lu J, Yang Y, et al. Stress-induced epinephrine enhances lactate dehydrogenase A and promotes breast cancer stem-like cells. J Clin Invest. (2019) 129:1030–46. doi: 10.1172/JCI121685
9. Chang A, Le CP, Walker AK, Creed SJ, Pon CK, Albold S, et al. β2-Adrenoceptors on tumor cells play a critical role in stress-enhanced metastasis in a mouse model of breast cancer. Brain Behav Immun. (2016) 57:106–15. doi: 10.1016/j.bbi.2016.06.011
10. Androulidaki A, Dermitzaki E, Venihaki M, Karagianni E, Rassouli O, Andreakou E, et al. Corticotropin releasing factor promotes breast cancer cell motility and invasiveness. Mol Cancer. (2009) 8:30. doi: 10.1186/1476-4598-8-30
13. Zhi X, Li B, Li Z, Zhang J, Yu J, Zhang L, et al. Adrenergic modulation of AMPKdependent autophagy by chronic stress enhances cell proliferation and survival in gastric cancer. Int J Oncol. (2019) 54:1625–38. doi: 10.3892/ijo.2019.4753
14. Zhang X, Zhang Y, He Z, Yin K, Li B, Zhang L, et al. Chronic stress promotes gastric cancer progression and metastasis: an essential role for ADRB2. Cell Death Dis. (2019) 10:788. doi: 10.1038/s41419-019-2030-2
15. Chen H, Liu D, Guo L, Cheng X, Guo N, Shi M. Chronic psychological stress promotes lung metastatic colonization of circulating breast cancer cells by decorating a pre-metastatic niche through activating beta-adrenergic signaling. J Pathol. (2018) 244:49–60. doi: 10.1002/path.4988
16. Jang HJ, Boo HJ, Lee HJ, Min HY, Lee HY. Chronic stress facilitates lung tumorigenesis by promoting exocytosis of IGF2 in lung epithelial cells. Cancer Res. (2016) 76:6607–19. doi: 10.1158/0008-5472.CAN-16-0990
18. Parker J, Klein SL, McClintock MK, Morison WL, Ye X, Conti CJ, et al. Chronic stress accelerates ultraviolet-induced cutaneous carcinogenesis. J Am Acad Dermatol. (2004) 51:919–22. doi: 10.1016/j.jaad.2004.08.042
21. Jung S, Choe S, Woo H, Jeong H, An HK, Moon H, et al. Autophagic death of neural stem cells mediates chronic stress-induced decline of adult hippocampal neurogenesis and cognitive deficits. Autophagy. (2019) 16:512–30. doi: 10.1080/15548627.2019.1630222
22. Salmaso N, Stevens HE, McNeill J, ElSayed M, Ren Q, Maragnoli ME, et al. Fibroblast growth factor 2 modulates hypothalamic pituitary axis activity and anxiety behavior through glucocorticoid receptors. Biol Psychiatry. (2016) 80:479–89. doi: 10.1016/j.biopsych.2016.02.026
23. McKlveen JM, Myers B, Flak JN, Bundzikova J, Solomon MB, Seroogy KB, et al. Role of prefrontal cortex glucocorticoid receptors in stress and emotion. Biol Psychiatry. (2013) 74:672–9. doi: 10.1016/j.biopsych.2013.03.024
25. Yang H, Xia L, Chen J, Zhang S, Martin V, Li Q, et al. Stress-glucocorticoid-TSC22D3 axis compromises therapy-induced antitumor immunity. Nat Med. (2019) 25:1428–41. doi: 10.1038/s41591-019-0566-4
26. Curtin NM, Boyle NT, Mills KH, Connor TJ. Psychological stress suppresses innate IFN-gamma production via glucocorticoid receptor activation: reversal by the anxiolytic chlordiazepoxide. Brain Behav Immun. (2009) 23:535–47. doi: 10.1016/j.bbi.2009.02.003
27. Feng Z, Liu L, Zhang C, Zheng T, Wang J, Lin M, et al. Chronic restraint stress attenuates p53 function and promotes tumorigenesis. Proc Natl Acad Sci USA. (2012) 109:7013–8. doi: 10.1073/pnas.1203930109
31. Zahalka AH, Arnal-Estape A, Maryanovich M, Nakahara F, Cruz CD, Finley LWS, et al. Adrenergic nerves activate an angio-metabolic switch in prostate cancer. Science. (2017) 358:321–6. doi: 10.1126/science.aah5072
33. Kim-Fuchs C, Le CP, Pimentel MA, Shackleford D, Ferrari D, Angst E, et al. Chronic stress accelerates pancreatic cancer growth and invasion: a critical role for beta-adrenergic signaling in the pancreatic microenvironment. Brain Behav Immun. (2014) 40:40–7. doi: 10.1016/j.bbi.2014.02.019
34. Thaker PH, Han LY, Kamat AA, Arevalo JM, Takahashi R, Lu C, et al. Chronic stress promotes tumor growth and angiogenesis in a mouse model of ovarian carcinoma. Nat Med. (2006) 12:939–44. doi: 10.1038/nm1447
35. Renz BW, Takahashi R, Tanaka T, Macchini M, Hayakawa Y, Dantes Z, et al. β2 Adrenergic-neurotrophin feedforward loop promotes pancreatic cancer. Cancer Cell. (2018) 33:75–90.e7. doi: 10.1016/j.ccell.2017.11.007
36. Armaiz-Pena GN, Allen JK, Cruz A, Stone RL, Nick AM, Lin YG, et al. Src activation by beta-adrenoreceptors is a key switch for tumour metastasis. Nat Commun. (2013) 4:1403. doi: 10.1038/ncomms2413
38. Hara MR, Kovacs JJ, Whalen EJ, Rajagopal S, Strachan RT, Grant W, et al. A stress response pathway regulates DNA damage through beta2-adrenoreceptors and beta-arrestin-1. Nature. (2011) 477:349–53. doi: 10.1038/nature10368
39. Landen CN Jr, Lin YG, Armaiz Pena GN, Das PD, Arevalo JM, Kamat AA, et al. Neuroendocrine modulation of signal transducer and activator of transcription-3 in ovarian cancer. Cancer Res. (2007) 67:10389–96. doi: 10.1158/0008-5472.CAN-07-0858
41. Zhang D, Ma Q, Wang Z, Zhang M, Guo K, Wang F, et al. β2-adrenoceptor blockage induces G1/S phase arrest and apoptosis in pancreatic cancer cells via Ras/Akt/NFkappaB pathway. Mol Cancer. (2011) 10:146. doi: 10.1186/1476-4598-10-146
43. Arranz A, Venihaki M, Mol B, Androulidaki A, Dermitzaki E, Rassouli O, et al. The impact of stress on tumor growth: peripheral CRF mediates tumor-promoting effects of stress. Mol Cancer. (2010) 9:261. doi: 10.1186/1476-4598-9-261
44. Frick LR, Rapanelli M, Bussmann UA, Klecha AJ, Arcos ML, Genaro AM, et al. Involvement of thyroid hormones in the alterations of T-cell immunity and tumor progression induced by chronic stress. Biol Psychiatry. (2009) 65:935–42. doi: 10.1016/j.biopsych.2008.12.013
46. Niraula A, Wang Y, Godbout JP, Sheridan JF. Corticosterone production during repeated social defeat causes monocyte mobilization from the bone marrow, glucocorticoid resistance, and neurovascular adhesion molecule expression. J Neurosci. (2018) 38:2328–40. doi: 10.1523/JNEUROSCI.2568-17.2018
47. Wohleb ES, Hanke ML, Corona AW, Powell ND, Stiner LM, Bailey MT, et al. β-Adrenergic receptor antagonism prevents anxiety-like behavior and microglial reactivity induced by repeated social defeat. J Neurosci. (2011) 31:6277–88. doi: 10.1523/JNEUROSCI.0450-11.2011
48. Hanke ML, Powell ND, Stiner LM, Bailey MT, Sheridan JF. Beta adrenergic blockade decreases the immunomodulatory effects of social disruption stress. Brain Behav Immun. (2012) 26:1150–9. doi: 10.1016/j.bbi.2012.07.011
49. Antoni MH, Lutgendorf SK, Blomberg B, Carver CS, Lechner S, Diaz A, et al. Cognitive-behavioral stress management reverses anxiety-related leukocyte transcriptional dynamics. Biol Psychiatry. (2012) 71:366–72. doi: 10.1016/j.biopsych.2011.10.007
59. Muthuswamy R, Okada NJ, Jenkins FJ, McGuire K, McAuliffe PF, Zeh HJ, et al. Epinephrine promotes COX-2-dependent immune suppression in myeloid cells and cancer tissues. Brain Behav Immun. (2017) 62:78–86. doi: 10.1016/j.bbi.2017.02.008
60. Le CP, Nowell CJ, Kim-Fuchs C, Botteri E, Hiller JG, Ismail H, et al. Chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination. Nat Commun. (2016) 7:10634. doi: 10.1038/ncomms10634
61. Vodicka M, Ergang P, Hrncir T, Mikulecka A, Kvapilova P, Vagnerova K, et al. Microbiota affects the expression of genes involved in HPA axis regulation and local metabolism of glucocorticoids in chronic psychosocial stress. Brain Behav Immun. (2018) 73:615–24. doi: 10.1016/j.bbi.2018.07.007
64. O'Mahony SM, Marchesi JR, Scully P, Codling C, Ceolho AM, Quigley EM, et al. Early life stress alters behavior, immunity, and microbiota in rats: implications for irritable bowel syndrome and psychiatric illnesses. Biol Psychiatry. (2009) 65:263–7. doi: 10.1016/j.biopsych.2008.06.026
65. Biondi M, Peronti M, Pacitti F, Pancheri P, Pacifici R, Altieri I, et al. Personality, endocrine and immune changes after eight months in healthy individuals under normal daily stress. Psychother Psychosom. (1994) 62:176–84. doi: 10.1159/000288920
67. Bird W, Adamo G, Pitini E, Gray M, Jani A. Reducing chronic stress to promote health in adults: the role of social prescriptions and social movements. J R Soc Med. (2020) 113:105–9. doi: 10.1177/0141076819890547
68. Wootten AC, Abbott JA, Meyer D, Chisholm K, Austin DW, Klein B, et al. Preliminary results of a randomised controlled trial of an online psychological intervention to reduce distress in men treated for localised prostate cancer. Eur Urol. (2015) 68:471–9. doi: 10.1016/j.eururo.2014.10.024
69. Breitbart W, Rosenfeld B, Pessin H, Applebaum A, Kulikowski J, Lichtenthal WG. Meaning-centered group psychotherapy: an effective intervention for improving psychological well-being in patients with advanced cancer. J Clin Oncol. (2015) 33:749–54. doi: 10.1200/JCO.2014.57.2198
70. Carayol M, Bernard P, Boiche J, Riou F, Mercier B, Cousson-Gelie F, et al. Psychological effect of exercise in women with breast cancer receiving adjuvant therapy: what is the optimal dose needed? Ann Oncol. (2013) 24:291–300. doi: 10.1093/annonc/mds342
71. Rodin G, Lo C, Rydall A, Shnall J, Malfitano C, Chiu A, et al. Managing cancer and living meaningfully (CALM): a randomized controlled trial of a psychological intervention for patients with advanced cancer. J Clin Oncol. (2018) 36:2422–32. doi: 10.1200/JCO.2017.77.1097
72. Witek Janusek L, Tell D, Mathews HL. Mindfulness based stress reduction provides psychological benefit and restores immune function of women newly diagnosed with breast cancer: a randomized trial with active control. Brain Behav Immun. (2019) 80:358–73. doi: 10.1016/j.bbi.2019.04.012
73. Lengacher CA, Reich RR, Paterson CL, Ramesar S, Park JY, Alinat C, et al. Examination of broad symptom improvement resulting from mindfulness-based stress reduction in breast cancer survivors: a randomized controlled trial. J Clin Oncol. (2016) 34:2827–34. doi: 10.1200/JCO.2015.65.7874
74. Chambers SK, Occhipinti S, Foley E, Clutton S, Legg M, Berry M, et al. Mindfulness-based cognitive therapy in advanced prostate cancer: a randomized controlled trial. J Clin Oncol. (2017) 35:291–7. doi: 10.1200/JCO.2016.68.8788
75. Xu L, Stevens J, Hilton MB, Seaman S, Conrads TP, Veenstra TD, et al. COX-2 inhibition potentiates antiangiogenic cancer therapy and prevents metastasis in preclinical models. Sci Transl Med. (2014) 6:242ra84. doi: 10.1126/scitranslmed.3008455
76. Moreno-Smith M, Lu C, Shahzad MM, Pena GN, Allen JK, Stone RL, et al. Dopamine blocks stress-mediated ovarian carcinoma growth. Clin Cancer Res. (2011) 17:3649–59. doi: 10.1158/1078-0432.CCR-10-2441
79. Ricon I, Hanalis-Miller T, Haldar R, Jacoby R, Ben-Eliyahu S. Perioperative biobehavioral interventions to prevent cancer recurrence through combined inhibition of beta-adrenergic and cyclooxygenase 2 signaling. Cancer. (2019) 125:45–56. doi: 10.1002/cncr.31594
80. Ramondetta LM, Hu W, Thaker PH, Urbauer DL, Chisholm GB, Westin SN, et al. Prospective pilot trial with combination of propranolol with chemotherapy in patients with epithelial ovarian cancer and evaluation on circulating immune cell gene expression. Gynecol Oncol. (2019) 154:524–30. doi: 10.1016/j.ygyno.2019.07.004
81. Chaudhary KR, Yan SX, Heilbroner SP, Sonett JR, Stoopler MB, Shu C, et al. Effects of beta-adrenergic antagonists on chemoradiation therapy for locally advanced non-small cell lung cancer. J Clin Med. (2019) 8:575. doi: 10.3390/jcm8050575
82. Haldar R, Shaashua L, Lavon H, Lyons YA, Zmora O, Sharon E, et al. Perioperative inhibition of beta-adrenergic and COX2 signaling in a clinical trial in breast cancer patients improves tumor Ki-67 expression, serum cytokine levels, and PBMCs transcriptome. Brain Behav Immun. (2018) 73:294–309. doi: 10.1016/j.bbi.2018.05.014
83. Spera G, Fresco R, Fung H, Dyck JRB, Pituskin E, Paterson I, et al. Beta blockers and improved progression-free survival in patients with advanced HER2 negative breast cancer: a retrospective analysis of the ROSE/TRIO-012 study. Ann Oncol. (2017) 28:1836–41. doi: 10.1093/annonc/mdx264
84. Shaashua L, Shabat-Simon M, Haldar R, Matzner P, Zmora O, Shabtai M, et al. Perioperative COX-2 and beta-adrenergic blockade improves metastatic biomarkers in breast cancer patients in a phase-II randomized trial. Clin Cancer Res. (2017) 23:4651–61. doi: 10.1158/1078-0432.CCR-17-0152
Keywords: stress, cancer, hormone, inflammation, immunity, hypothalamic-pituitary-adrenal axis, corticosteroids, catecholamines
Citation: Dai S, Mo Y, Wang Y, Xiang B, Liao Q, Zhou M, Li X, Li Y, Xiong W, Li G, Guo C and Zeng Z (2020) Chronic Stress Promotes Cancer Development. Front. Oncol. 10:1492. doi: 10.3389/fonc.2020.01492
Received: 08 April 2020; Accepted: 13 July 2020;
Published: 19 August 2020.
Edited by:Sridhar Muthusami, Karpagam Academy of Higher Education, India
Reviewed by:Ravi Manoharan, University of Madras, India
Aruljothi Muralidharan, University of California School of Medicine, Riverside, United States
Copyright © 2020 Dai, Mo, Wang, Xiang, Liao, Zhou, Li, Li, Xiong, Li, Guo and Zeng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Zhaoyang Zeng, firstname.lastname@example.org