Muscarinic Receptors Associated with Cancer

被引:12
作者
Calaf, Gloria M. [1 ]
Crispin, Leodan A. [1 ]
Munoz, Juan P. [1 ]
Aguayo, Francisco [2 ]
Bleak, Tammy C. [1 ]
机构
[1] Univ Tarapaca, Inst Alta Invest, Arica 1000000, Chile
[2] Univ Chile, Fac Med, Inst Ciencias Biomed ICBM, Programa Virol,Lab Oncovirol, Santiago 8380000, Chile
关键词
muscarinic receptors; breast; gastric; lung; colorectal; prostate; glioblastoma; liver; cancer; EPIDERMAL-GROWTH-FACTOR; EPITHELIAL-CELL PROLIFERATION; TYROSINE KINASE INHIBITORS; ACTIVATED PROTEIN-KINASE; GENE-EXPRESSION PATTERNS; NITRIC-OXIDE SYNTHASE; BREAST-CANCER; LUNG-CANCER; HEPATOCELLULAR-CARCINOMA; GASTRIC-CANCER;
D O I
10.3390/cancers14092322
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Recently, cancer research has described the presence of the cholinergic machinery, specifically muscarinic receptors, in a wide variety of cancers due to their activation and signaling pathways associated with tumor progression and metastasis, providing a wide overview of their contribution to different cancer formation and development for new antitumor targets. This review focused on determining the molecular signatures associated with muscarinic receptors in breast and other cancers and the need for pharmacological, molecular, biochemical, technological, and clinical approaches to improve new therapeutic targets. Cancer has been considered the pathology of the century and factors such as the environment may play an important etiological role. The ability of muscarinic agonists to stimulate growth and muscarinic receptor antagonists to inhibit tumor growth has been demonstrated for breast, melanoma, lung, gastric, colon, pancreatic, ovarian, prostate, and brain cancer. This work aimed to study the correlation between epidermal growth factor receptors and cholinergic muscarinic receptors, the survival differences adjusted by the stage clinical factor, and the association between gene expression and immune infiltration level in breast, lung, stomach, colon, liver, prostate, and glioblastoma human cancers. Thus, targeting cholinergic muscarinic receptors appears to be an attractive therapeutic alternative due to the complex signaling pathways involved.
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页数:32
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