Expression of the putative cannabinoid receptor GPR55 is increased in endometrial carcinoma

被引:6
|
作者
Ayakannu, Thangesweran [1 ,2 ,3 ]
Taylor, Anthony H. [3 ,4 ]
Konje, Justin C. [3 ,5 ]
机构
[1] Univ Liverpool, Fac Hlth & Life Sci, Liverpool, Merseyside, England
[2] Liverpool Womens NHS Fdn Trust, Liverpool Womens Hosp, Gynaecol Oncol Ctr, Dept Obstet & Gynaecol, Liverpool, Merseyside, England
[3] Univ Leicester, Dept Canc Studies & Mol Med, Endocannabinoid Res Grp, Reprod Sci Sect, Leicester, Leics, England
[4] Univ Leicester, George Davies Ctr Med, Dept Mol & Cell Biol, Univ Rd, Leicester LE2 7RH, Leics, England
[5] Univ Leicester, Dept Hlth Sci, Leicester, Leics, England
关键词
GPR55; N-Acylethanolamine; Cannabinoid receptors; Endometrial cancer; Gene expression; Immunohistochemistry; GENE-EXPRESSION; CANCER; LYSOPHOSPHATIDYLINOSITOL; OBESITY; LYSOPHOSPHOLIPIDS; IDENTIFICATION; PROLIFERATION; REVEALS; SYSTEM; TRENDS;
D O I
10.1007/s00418-021-02018-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although the expression of the putative cannabinoid receptor GPR55 has been shown to be involved in the growth of various tumours and is increased in a number of cancers, its expression has not been examined in patients with endometrial cancer (EC). Quantitative RT-PCR (for mRNA levels) and immunohistochemistry (for protein levels) were used to measure GPR55 expression in patients with Type 1 and Type 2 EC and correlated against cannabinoid receptor (CB1 and CB2) protein levels using non-cancerous endometrium as the control tissue. The data indicated that GPR55 transcript and GPR55 protein levels were significantly (p < 0.002 and p < 0.0001, respectively) higher in EC tissues than in control tissues. The levels of immunoreactive GPR55 protein were correlated with GPR55 transcript levels, but not with the expression of CB1 receptor protein, and were inversely correlated with CB2 protein expression, which was significantly decreased. It can be concluded that GPR55 expression is elevated in women with EC, and thus could provide a potential novel biomarker and therapeutic target for this disease.
引用
收藏
页码:449 / 460
页数:12
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