Caffeine promotes anti-tumor immune response during tumor initiation: Involvement of the adenosine A_2A receptor

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• 作者：Hadar Eini^a ; ^{einyh@post.bgu.ac.il" class="auth_mail" title="E-mail the corresponding author} ; Valeria Frishman^a ; ^{fischman@bgu.ac.il" class="auth_mail" title="E-mail the corresponding author} ; Robert Yulzari^b ; ^{roberty@clalit.org.il" class="auth_mail" title="E-mail the corresponding author} ; Leonid Kachko^c ; ^{leonidka@clalit.org.il" class="auth_mail" title="E-mail the corresponding author} ; Eli C. Lewis^a ; ^{lewis@bgu.ac.il" class="auth_mail" title="E-mail the corresponding author} ; Cidio Chaimovitz^b ; ^{cidio@bgu.ac.il" class="auth_mail" title="E-mail the corresponding author} ; Amos Douvdevani^a ; ^b ; ^{amosd@bgu.ac.il" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Adenosine ; A2AR ; Caffeine ; 3-MCA ; Anti-tumor immunity
• 刊名：Biochemical Pharmacology
• 出版年：2015
• 出版时间：1 November 2015
• 年：2015
• 卷：98
• 期：1
• 页码：110-118
• 全文大小：1682 K

文摘

Epidemiologic studies depict a negative correlation between caffeine consumption and incidence of tumors in humans. The main pharmacological effects of caffeine are mediated by antagonism of the adenosine receptor, A_2AR. Here, we examine whether the targeting of A_2AR by caffeine plays a role in anti-tumor immunity. In particular, the effects of caffeine are studied in wild-type and A_2AR knockout (A_2AR^−/−) mice. Tumor induction was achieved using the carcinogen 3-methylcholanthrene (3-MCA). Alternatively, tumor cells, comprised of 3-MCA–induced transformed cells or B16 melanoma cells, were inoculated into animal footpads. Cytokine release was determined in a mixed lymphocyte tumor reaction (MLTR). According to our findings, caffeine-consuming mice (0.1% in water) developed tumors at a lower rate compared to water-consuming mice (14% vs. 53%, respectively, p = 0.0286, n = 15/group). Within the caffeine-consuming mice, tumor-free mice displayed signs of autoimmune alopecia and pronounced leukocyte recruitment intocarcinogen injection sites. Similarly, A_2AR^−/− mice exhibited reduced rates of 3-MCA-induced tumors. In tumor inoculation studies, caffeine treatment resulted in inhibition of tumor growth and elevation in proinflammatory cytokine release over water-consuming mice, as depicted by MLTR. Addition of the adenosine receptor agonist, NECA, to MLTR resulted in a sharp decrease in IFN纬 levels; this was reversed by the highly selective A_2AR antagonist, ZM241385. Thus, immune response modulation through either caffeine or genetic deletion of A_2AR leads to a Th1 immune profile and suppression of carcinogen-induced tumorigenesis. Taken together, our data suggest that the use of pharmacologic A_2AR antagonists may hold therapeutic potential in diminishing the rate of cancer development.