Adenosine Receptors as Novel Targets for the Treatment of Various Cancers

被引:22
作者
Gorain, Bapi [1 ]
Choudhury, Hira [2 ]
Yee, Gan Sook [3 ]
Bhattamisra, Subrat Kumar [3 ]
机构
[1] Taylors Univ, Fac Hlth & Med Sci, Sch Pharm, Subang Jaya, Selangor, Malaysia
[2] Int Med Univ, Sch Pharm, Dept Pharmaceut Technol, Kuala Lumpur 57000, Malaysia
[3] Int Med Univ, Sch Pharm, Dept Life Sci, Kuala Lumpur 57000, Malaysia
关键词
Adenosine; adenosine receptors; receptor modulators; cancer; signalling pathways; tumour cell; FACTOR-KAPPA-B; CELL-CYCLE ARREST; CL-IB-MECA; BREAST-CANCER; A(2A) RECEPTORS; TUMOR-GROWTH; HEPATOCELLULAR-CARCINOMA; DIFFERENTIAL EXPRESSION; CIITA TRANSCRIPTION; ESTROGEN-RECEPTOR;
D O I
10.2174/1381612825666190716102037
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Adenosine is a ubiquitous signaling nucleoside molecule, released from different cells within the body to act on vasculature and immunoescape. The physiological action on the proliferation of tumour cell has been reported by the presence of high concentration of adenosine within the tumour microenvironment, which results in the progression of the tumour, even leading to metastases. The activity of adenosine exclusively depends upon the interaction with four subtypes of heterodimeric G-protein-coupled adenosine receptors (AR), A(1), A(2A), A(2B), and A(3)-ARs on the cell surface. Research evidence supports that the activation of those receptors via specific agonist or antagonist can modulate the proliferation of tumour cells. The first category of AR,A(1) is known to play an antitumour activity via tumour-associated microglial cells to prevent the development of glioblastomas. A(2A)AR are found in melanoma, lung, and breast cancer cells, where tumour proliferation is stimulated due to inhibition of the immune response via inhibition of natural killer cells cytotoxicity, T cell activity, and tumour-specific CD4+/CD8+ activity. Alternatively, A(2B)AR helps in the development of tumour upon activation via upregulation of angiogenin factor in the microvascular endothelial cells, inhibition of MAPK and ERK 1/2 phosphorylation activity. Lastly, A(3)AR is expressed in low levels in normal cells whereas the expression is upregulated in tumour cells, however, agonists to this receptor inhibit tumour proliferation through modulation of Wnt and NE-kappa B signaling pathways. Several researchers are in search for potential agents to modulate the overexpressed ARs to control cancer. Active components of A(2)AAR antagonists and A(3)AR agonists have already entered in Phase-1 clinical research to prove their safety in human. This review focused on novel research targets towards the prevention of cancer progression through stimulation of the overexpressed ARs with the hope to protect lives and advance human health.
引用
收藏
页码:2828 / 2841
页数:14
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