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• W1487341279 abstract "// Guillermo N. Armaiz-Pena 1 , Vianey Gonzalez-Villasana 2 , Archana S. Nagaraja 1 , Cristian Rodriguez-Aguayo 2 , Nouara C. Sadaoui 1 , Rebecca L. Stone 3 , Koji Matsuo 4 , Heather J. Dalton 1 , Rebecca A. Previs 1 , Nicholas B. Jennings 1 , Piotr Dorniak 1 , Jean M. Hansen 1 , Jesusa M.G. Arevalo 5 , Steve W. Cole 5 , Susan K. Lutgendorf 6 , Anil K. Sood 1, 7, 8 , Gabriel Lopez-Berestein 2, 7, 8 1 Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA 2 Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA 3 Department of Obstetrics and Gynecology, The John Hopkins University, Baltimore, MD 21287, USA 4 Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Southern California, Los Angeles, CA 90089, USA 5 Department of Medicine, Division of Hematology-Oncology, University of California, Los Angeles, CA 90095, USA 6 Department of Psychology, Obstetrics and Urology, and Holden Comprehensive Cancer Center, University of Iowa, Iowa City, Iowa 52242, USA 7 Department of Cancer Biology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA 8 Center for RNA Interference and Non-coding RNA, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA Correspondence to: Gabriel Lopez-Berestein, e-mail: glopez@mdanderson.org Keywords: ovarian cancer, macrophages, monocytes, catecholamines, MCP1 Received: September 15, 2014      Accepted: December 09, 2014      Published: December 27, 2014 ABSTRACT Increased adrenergic signaling facilitates tumor progression, but the underlying mechanisms remain poorly understood. We examined factors responsible for stress-mediated effects on monocyte/macrophage recruitment into the tumor microenvironment, and the resultant effects on tumor growth. In vitro , MCP1 was significantly increased after catecholamine exposure, which was mediated by cAMP and PKA. Tumor samples from mice subjected to daily restraint stress had elevated MCP1 gene and protein levels, increased CD14+ cells, and increased infiltration of CD68+ cells. hMCP1 siRNA-DOPC nanoparticles significantly abrogated daily restraint stress-induced tumor growth and inhibited infiltration of CD68+ and F4/80+ cells. In ovarian cancer patients, elevated peripheral blood monocytes and tumoral macrophages were associated with worse overall survival. Collectively, we demonstrate that increased adrenergic signaling is associated with macrophage infiltration and mediated by tumor cell-derived MCP1 production." @default.
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• W1487341279 date "2014-12-27" @default.
• W1487341279 modified "2023-10-18" @default.
• W1487341279 title "Adrenergic regulation of monocyte chemotactic protein 1 leads to enhanced macrophage recruitment and ovarian carcinoma growth" @default.
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• W1487341279 doi "https://doi.org/10.18632/oncotarget.2887" @default.
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