Khoo H E, Ho C L, Chhatwal V J, Chan S T, Ngoi S S, Moochhala S M
Department of Biochemistry and Surgery, National University of Singapore, Singapore.
Cancer Lett. 1996 Aug 23;106(1):17-21. doi: 10.1016/0304-3835(96)04289-9.
Adenosine A1 receptors (A1R) are known to inhibit while the A2 receptors (A2R) stimulate the G-protein cAMP second messenger system and may play a role in cell growth and carcinogenesis. Using a quantitative reverse transcription-polymerase chain reaction (RT-PCR) method, mRNA for A1R and A2R was measured in human colorectal adenocarcinomas and individual peritumoural colon tissues. There was differential expression of the mRNA for A1R with tumour tissues having significantly higher amounts compared to peritumoural normal tissues. The mRNA for A2R was not found to be differentially expressed. The increase in the inhibitory A1 receptor in tumour tissues may be in response to increased adenosine release from the hypoxic cells found in malignant tumour tissues, thus indicating a possible role for the adenosine A1 receptor in carcinogenesis.
已知腺苷A1受体(A1R)具有抑制作用,而A2受体(A2R)则刺激G蛋白cAMP第二信使系统,并且可能在细胞生长和致癌作用中发挥作用。采用定量逆转录-聚合酶链反应(RT-PCR)方法,检测了人类结肠腺癌及各个癌旁结肠组织中A1R和A2R的信使核糖核酸(mRNA)。A1R的mRNA存在差异表达,肿瘤组织中的含量明显高于癌旁正常组织。未发现A2R的mRNA存在差异表达。肿瘤组织中抑制性A1受体的增加可能是对恶性肿瘤组织中缺氧细胞释放的腺苷增加所作出的反应,从而表明腺苷A1受体在致癌作用中可能发挥作用。