| Literature DB >> 29515233 |
Yan Cheng1, Xing-Hua Gao1, Xian-Jing Li1, Qiu-Hua Cao1, Dan-Dan Zhao1, Jin-Rong Zhou2, Hong-Xi Wu1, Yun Wang1, Lin-Jun You1, Hong-Bao Yang1, Yun-Long He1, Yong-Ren Li1, Jin-Song Bian3, Qing-Yi Zhu4, Lutz Birnbaumer5,6, Yong Yang7.
Abstract
Depression drives cancer progression and induces poor clinical outcome. However, the mechanisms underlying depression and cancer outcomes are unclear. In this work, we investigated 98 prostate cancer patients and found that patients with high score of psychological depression were correlated with tumor invasion and metastasis. We found focal adhesion kinase (FAK) was increased in cancer patients with metastatic features and high score of depression. FAK knockdown completely blocked depression-promoted tumor invasion in orthotopic transplantation tumors. In Hi-myc mice and a murine model of depression, sympathetic activation was detected in the prostate tissue. Further we showed that FAK activation was dependent on a cAMP-PKA signaling pathway. Our results demonstrated that the activation of a sympathetic-FAK signaling pathway in prostate cancer patients with high degrees of depression facilitates tumor invasion. We suggest that blocking β2AR with propranolol or inhibiting FAK activation with PF562 271 may be novel strategies for depressed patients with invasive prostate cancer.Entities:
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Year: 2018 PMID: 29515233 DOI: 10.1038/s41388-018-0177-4
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867