Zehentner Sofie, Reiner Agnes T, Grimm Christoph, Somoza Veronika
Department of Physiological Chemistry, Faculty of Chemistry, University of Vienna, 1090 Vienna, Austria.
Comprehensive Cancer Center Vienna, Gynecologic Cancer Unit, Department of General Gynecology and Gynecologic Oncology, Medical University of Vienna, 1090 Vienna, Austria.
Cancers (Basel). 2021 Nov 23;13(23):5891. doi: 10.3390/cancers13235891.
Since it is known that bitter taste receptors (TAS2Rs) are expressed and functionally active in various extra-oral cells, their genetic variability and functional response initiated by their activation have become of broader interest, including in the context of cancer.
A systematic research was performed in PubMed and Google Scholar to identify relevant publications concerning the role of TAS2Rs in cancer.
While the findings on variations of TAS2R genotypes and phenotypes and their association to the risk of developing cancer are still inconclusive, gene expression analyses revealed that TAS2Rs are expressed and some of them are predominately downregulated in cancerous compared to non-cancerous cell lines and tissue samples. Additionally, receptor-specific, agonist-mediated activation induced various anti-cancer effects, such as decreased cell proliferation, migration, and invasion, as well as increased apoptosis. Furthermore, the overexpression of TAS2Rs resulted in a decreased tumour incidence in an in vivo study and TAS2R activation could even enhance the therapeutic effect of chemotherapeutics in vitro. Finally, higher expression levels of TAS2Rs in primary cancerous cells and tissues were associated with an improved prognosis in humans.
Since current evidence demonstrates a functional role of TAS2Rs in carcinogenesis, further studies should exploit their potential as (co-)targets of chemotherapeutics.
由于已知苦味受体(TAS2Rs)在各种口腔外细胞中表达且具有功能活性,其基因变异性以及激活引发的功能反应已引起更广泛关注,包括在癌症背景下。
在PubMed和谷歌学术上进行了系统研究,以确定有关TAS2Rs在癌症中作用的相关出版物。
虽然关于TAS2R基因型和表型变异及其与患癌风险关联的研究结果仍无定论,但基因表达分析显示,与非癌细胞系和组织样本相比,TAS2Rs在癌细胞中表达,其中一些主要下调。此外,受体特异性激动剂介导的激活诱导了多种抗癌作用,如细胞增殖、迁移和侵袭减少,以及细胞凋亡增加。此外,在一项体内研究中,TAS2Rs的过表达导致肿瘤发生率降低,TAS2R激活甚至可以增强化疗药物在体外的治疗效果。最后,原发性癌细胞和组织中TAS2Rs的较高表达水平与人类预后改善相关。
由于目前的证据表明TAS2Rs在致癌过程中具有功能作用,进一步的研究应探索其作为化疗药物(共同)靶点的潜力。