Background:Our previous study demonstrated that extracellular adenosine 5′-triphosphate (ATP) stimulated prostate cancer cell invasion via P2Y receptors. However, the purinergic receptor subtype(s) involved in this process remains unclear. Here we aimed to determine whether P2Y2, one subtype of P2Y receptors, was involved in the invasion and metastasis of prostate cancer cells, and elucidated the underlying mechanism.Methods:RNAi was introduced to silence the expression of P2Y2. In vitro invasion and migration assays and in vivo experiments were carried out to examine the role of P2Y2 receptor in cell invasion and metastasis. cDNA microarray was performed to identify the differentially expressed genes downstream of ATP treatment.Results:P2Y2 was significantly expressed in the prostate cancer cells. Knockdown of P2Y2 receptor suppressed cell invasion and metastasis in vitro and in vivo. Further experiments identified that ATP could promote IL-8 and Snail expression and inhibit E-cadherin and Claudin-1 expression. Knockdown of P2Y2 receptor affected the expression of these EMT/invasion-related genes in vitro and in vivo.Conclusion:P2Y2 receptor promotes cell invasion and metastasis in prostate cancer cells via some EMT/invasion-related genes. Thereby, P2Y2 receptor could be a potential therapeutic target for the treatment of prostate cancer.

Neutron scattering has been used to study the magnetic order of the Er ions in superconducting ErBa2Cu307. Above the 3D Neel temperature (7"^^ =0.618 K) a rod of scattering characteristic of 2D behavior is unambiguously observed, showing that the magnetic interactions of the rare-earth ions are highly anisotropic; below TN the order parameter follows the exact Onsager solution for a 2D Ising antiferromagnet. At low T, two separate types of simple 3D antiferromagnetic structures are found, one characterized by a wave vector of (y ,0,0), and the other by (y ,0, y ).

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