Artículo
Depression promotes prostate cancer invasion and metastasis via a sympathetic-cAMP-FAK signaling pathway
Cheng, Yan; Gao, Xing Hua; Li, Xian Jing; Cao, Qiu Hua; Zhao, Dan Dan; Zhou, Jin Rong; Wu, Hong Xi; Wang, Yun; You, Lin Jun; Yang, Hong Bao; He, Yun Long; Li, Yong Ren; Bian, Jin Song; Zhu, Qing Yi; Birnbaumer, Lutz
; Yang, Yong
Fecha de publicación:
03/2018
Editorial:
Nature Publishing Group
Revista:
Oncogene
ISSN:
0950-9232
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
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.
Palabras clave:
prostate cancer invasion
,
metastasis via a sympathetic-cAMP-FAK
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Articulos(BIOMED)
Articulos de INSTITUTO DE INVESTIGACIONES BIOMEDICAS
Articulos de INSTITUTO DE INVESTIGACIONES BIOMEDICAS
Citación
Cheng, Yan; Gao, Xing Hua; Li, Xian Jing; Cao, Qiu Hua; Zhao, Dan Dan; et al.; Depression promotes prostate cancer invasion and metastasis via a sympathetic-cAMP-FAK signaling pathway; Nature Publishing Group; Oncogene; 37; 3-2018; 2953 - 2966
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