Chronic stress enhances progression of acute lymphoblastic leukemia via β-adrenergic signaling.

TitleChronic stress enhances progression of acute lymphoblastic leukemia via β-adrenergic signaling.
Publication TypeJournal Article
Year of Publication2012
AuthorsLamkin DM, Sloan EK, Patel AJ, Chiang BS, Pimentel MA, C Y Ma J, Arevalo JM, Morizono K, Cole SW
JournalBrain Behav Immun
Volume26
Issue4
Pagination635-41
Date Published2012 May
ISSN1090-2139
KeywordsAdrenergic beta-Antagonists, Animals, Cell Line, Tumor, Cyclic AMP, Disease Models, Animal, Disease Progression, Humans, Leukemia, Experimental, Male, Mice, Mice, SCID, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Propranolol, Receptors, Adrenergic, beta-1, Receptors, Adrenergic, beta-3, Restraint, Physical, Signal Transduction, Stress, Psychological
Abstract

Clinical studies suggest that stress-related biobehavioral factors can accelerate the progression of hematopoietic cancers such as acute lymphoblastic leukemia (ALL), but it is unclear whether such effects are causal or what biological pathways mediate such effects. Given the network of sympathetic nervous system (SNS) fibers that innervates the bone marrow to regulate normal (non-leukemic) hematopoietic progenitor cells, we tested the possibility that stress-induced SNS signaling might also affect ALL progression. In an orthotopic mouse model, Nalm-6 human pre-B ALL cells were transduced with the luciferase gene for longitudinal bioluminescent imaging and injected i.v. into male SCID mice for bone marrow engraftment. Two weeks of daily restraint stress significantly enhanced ALL tumor burden and dissemination in comparison to controls, and this effect was blocked by the β-adrenergic antagonist, propranolol. Although Nalm-6 ALL cells expressed mRNA for β1- and β3-adrenergic receptors, they showed no evidence of cAMP signaling in response to norepinephrine, and norepinephrine failed to enhance Nalm-6 proliferation in vitro. These results show that chronic stress can accelerate the progression of human pre-B ALL tumor load via a β-adrenergic signaling pathway that likely involves indirect regulation of ALL biology via alterations in the function of other host cell types such as immune cells or the bone marrow microenvironment.

DOI10.1016/j.bbi.2012.01.013
Alternate JournalBrain Behav. Immun.
PubMed ID22306453
PubMed Central IDPMC3322262
Grant ListAI28697 / AI / NIAID NIH HHS / United States
CA116778 / CA / NCI NIH HHS / United States
CA138687 / CA / NCI NIH HHS / United States
CA16042 / CA / NCI NIH HHS / United States
R01 CA116778 / CA / NCI NIH HHS / United States
R01 CA116778-05 / CA / NCI NIH HHS / United States
R01 CA160890 / CA / NCI NIH HHS / United States
R21 CA138687 / CA / NCI NIH HHS / United States
R21 CA138687-02 / CA / NCI NIH HHS / United States
T32 MH019925 / MH / NIMH NIH HHS / United States
T32 MH019925-15 / MH / NIMH NIH HHS / United States
T32-MH19925 / MH / NIMH NIH HHS / United States