Affiliation:
1. Department of Pharmacy, Zhangjiagang Second People's Hospital, Zhangjiagang 215600, Jiangsu, China
2. Department of Pharmacology, Pharmacy College, Nantong University, Nantong 226001, Jiangsu, China
Abstract
:
Human G protein-coupled receptor 56 (GPR56) belongs to a member of the adhesion
G-protein coupled receptor (aGPCR) family and widely exists in the central nervous system and
various types of tumor tissues. Recent studies have shown that abnormal expression or dysfunction
of GPR56 is closely associated with many physiological and pathological processes, including
brain development, neuropsychiatric disorders, cardiovascular diseases and cancer progression.
In addition, GPR56 has been proven to enhance the susceptibility of some antipsychotics and
anticarcinogens in response to the treatment of neuropsychological diseases and cancer. Although
there have been some reports about the functions of GPR56, the underlying mechanisms implicated
in these diseases have not been clarified thoroughly, especially in depression and epilepsy.
Therefore, in this review, we described the molecular structure and signal transduction pathway of
GPR56 and carried out a comprehensive summary of GPR56's function in the development of
psychiatric disorders and cancer. Our review showed that GPR56 deficiency led to depressive-like
behaviors and an increase in resistance to antipsychotic treatment. In contrast, the upregulation of
GPR56 contributed to tumor cell proliferation and metastasis in malignant diseases such as
glioblastoma, colorectal cancer, and ovarian cancer. Moreover, we elucidated specific signaling
pathways downstream of GPR56 related to the pathogenesis of these diseases. In summary, our review
provides compelling arguments for an attractive therapeutic target of GPR56 in improving
the therapeutic efficiency for patients suffering from psychiatric disorders and cancer.
Publisher
Bentham Science Publishers Ltd.