p53 upregulates PLCε-IP3-Ca2+ pathway and inhibits autophagy through its target gene Rap2B

The tumor suppressor p53 plays a pivotal role in numerous cellular responses as it regulates cell proliferation, metabolism, cellular growth, and autophagy. In order to identify novel p53 target genes, we utilized an unbiased microarray approach and identified Rap2B as a robust candidate, which belongs to the Ras-related GTP-binding protein superfamily and exhibits increased expression in various human cancers. We demonstrated that p53 increases the intracellular IP3 and Ca2+ levels and decreases the LC3 protein levels through its target gene Rap2B, suggesting that p53 can inhibit the autophagic response triggered by starvation via upregulation of the Rap2B-PLCε-IP3-Ca2+ pathway. As a confirmed target gene of p53, we believe that further investigating potential functions of Rap2B in autophagy and tumorigenesis will provide a novel strategy for cancer therapy

Rap2B promotes proliferation, migration and invasion of human breast cancer through calcium-related ERK1/2 signaling pathway

Rap2B, a member of GTP-binding proteins, is widely upregulated in many types of tumors and promotes migration and invasion of human suprarenal epithelioma. However, the function of Rap2B in breast cancer is unknown. Expression of Rap2B was examined in breast cancer cell lines and human normal breast cell line using Western blot analysis. Using the CCK-8 cell proliferation assay, cell cycle analysis, and transwell migration assay, we also elucidated the role of Rap2B in breast cancer cell proliferation, migration, and invasion. Results showed that the expression of Rap2B is higher in tumor cells than in normal cells. Flow cytometry and Western blot analysis revealed that Rap2B elevates the intracellular calcium level and further promotes extracellular signal-related kinase (ERK) 1/2 phosphorylation. By contrast, calcium chelator BAPTM/AM and MEK inhibitor (U0126) can reverse Rap2B-induced ERK1/2 phosphorylation. Furthermore, Rap2B knockdown inhibits cell proliferation, migration, and invasion abilities via calcium related-ERK1/2 signaling. In addition, overexpression of Rap2B promotes cell proliferation, migration and invasion abilities, which could be neutralized by BAPTM/AM and U0126. Taken together, these findings shed light on Rap2B as a therapeutic target for breast cancer

Modeling for WMd

The role of ensemble average differs in working memory for depth and planar informatio

Design and Simulation of Compound Eye Lens for Visible Light Communication and Illumination

We proposed a scheme for designing an optical launch system that can make the light intensity more uniform on the receiving plane via a compound eye lens combined with a sunflower plano-convex lens. The simulation results demonstrate that the light converges on the optical axis after passing through the sunflower-shaped plano-convex lens array and compound eye lens. The divergence angle and central light intensity of the receiving plane are, respectively, 26.57° and 80.50% of the total emitted light power for the array structure of the compact compound eye plano-convex lens, while those are 21.80° and 62.50% for the discrete compound eye lens. From the above results, it can be seen that the compact compound eye lens is more conducive to the uniform distribution of light intensity on the receiving plane compared with the discrete compound eye lens, taking into account the dual application of illumination and communication

The Short-Term Retention of Depth

We review research on the visual working memory for information portrayed by items arranged in depth (i.e., distance to the observer) within peri-personal space. Most items lose their metric depths within half a second, even though their identities and spatial positions are retained. The paradoxical loss of depth information may arise because visual working memory retains the depth of a single object for the purpose of actions such as pointing or grasping which usually apply to only one thing at a time