Ramos-Espiritu Lavoisier, Diaz Ana, Nardin Charlee, Saviola Anthony J, Shaw Fiona, Plitt Tamar, Yang Xia, Wolchok Jedd, Pirog Edyta C, Desman Garrett, Sboner Andrea, Zhang Tuo, Xiang Jenny, Merghoub Taha, Levin Lonny R, Buck Jochen, Zippin Jonathan H
Department of Pharmacology, Weill Cornell Medical College, New York, NY, USA.
Department of Dermatology, Weill Cornell Medical College, New York, NY, USA.
Oncotarget. 2016 Jul 19;7(29):45597-45607. doi: 10.18632/oncotarget.10056.
cAMP signaling pathways can both stimulate and inhibit the development of cancer; however, the sources of cAMP important for tumorigenesis remain poorly understood. Soluble adenylyl cyclase (sAC) is a non-canonical, evolutionarily conserved, nutrient- and pH-sensing source of cAMP. sAC has been implicated in the metastatic potential of certain cancers, and it is differentially localized in human cancers as compared to benign tissues. We now show that sAC expression is reduced in many human cancers. Loss of sAC increases cellular transformation in vitro and malignant progression in vivo. These data identify the metabolic/pH sensor soluble adenylyl cyclase as a previously unappreciated tumor suppressor protein.
环磷酸腺苷(cAMP)信号通路既能刺激也能抑制癌症的发展;然而,对于肿瘤发生至关重要的cAMP来源仍知之甚少。可溶性腺苷酸环化酶(sAC)是一种非典型的、进化保守的、对营养物质和pH敏感的cAMP来源。sAC与某些癌症的转移潜能有关,与良性组织相比,它在人类癌症中的定位存在差异。我们现在表明,sAC在许多人类癌症中表达降低。sAC的缺失会增加体外细胞转化和体内恶性进展。这些数据表明,代谢/pH传感器可溶性腺苷酸环化酶是一种此前未被认识的肿瘤抑制蛋白。