There is increasing evidence that circular RNA (circRNA) are involved in cancer development, but the regulation and function of human circRNA remain largely unknown. In this study, we demonstrated that ZKSCAN1, a zinc finger family gene, is expressed in both linear and circular (circZKSCAN1) forms of RNA in human hepatocellular carcinoma (HCC) tissues and cell lines. Here, we analyzed a cohort of 102 patients and found that expression of both ZKSCAN1 mRNA and circZKSCAN1 was significantly lower (P < 0.05) in the HCC samples compared with that in matched adjacent nontumorous tissues by reverse transcription PCR (RT‐PCR). The low expression level of ZKSCAN1 was only associated with tumor size (P = 0.032), while the cirZKSCAN1 levels varied in patients with different tumor numbers (P < 0.01), cirrhosis (P = 0.031), vascular invasion (P = 0.002), or microscopic vascular invasion (P = 0.002), as well as with the tumor grade (P < 0.001). Silencing both ZKSCAN1 mRNA and circZKSCAN1 promoted cell proliferation, migration, and invasion. In contrast, overexpression of both forms of RNA repressed HCC progression in vivo and in vitro. Silencing or overexpression of both forms of RNA did not interfere with each other. RNA‐seq revealed a very different molecular basis for the observed effects; ZKSCAN1 mRNA mainly regulated cellular metabolism, while circZKSCAN1 mediated several cancer‐related signaling pathways, suggesting a nonredundant role for ZKSCAN1 mRNA and circRNA. In conclusion, our results revealed two post‐translational products (ZKSCAN1 mRNA and circZKSCAN1) that cooperated closely with one another to inhibit growth, migration, and invasion of HCC. cirZKSCAN1 might be a useful marker for the diagnosis of HCC.

Both antigravity directional water transport and ultrafast evaporation are critical to achieving a high-performance moisture-wicking fabric. The transpiration in vascular plants possess both of these features, which is due to their optimized hierarchical structure composed of multibranching porous networks following Murray’s law. However, it remains a great challenge to simultaneously realize the ultrafast water transport and evaporation by mimicking nature’s Murray networks in the synthetic materials. Here, we report a synergistic assembly strategy to create a biomimetic micro- and nanofibrous membrane with antigravity directional water transport and quick-dry performance by combining a multibranching porous structure and surface energy gradient, overcoming previous limitations. The resulting fiber-based porous Murray membranes exhibit an ultrahigh one-way transport capability (R) of 1245%, a desired overall moisture management capability (OMMC) of 0.94, and an outstanding water evaporation rate of 0.67 g h–1 (5.8 and 2.1 times higher than the cotton fabric and Coolmax fabric, respectively). Overall, the successful synthesis of these biomimetic porous Murray membranes should serve as a source of inspiration for the development of moisture-wicking technologies, providing personal comfort in hot or humid environments.

Directional water transport is a predominant part of functional textiles used for continuous sweat release in daily life. However, it has remained a great challenge to design such textiles which ensure continuous directional water transport and superior prevention of water penetration in the reverse direction. Here, a scalable strategy is reported to create trilayered fibrous membranes with progressive wettability by introducing a transfer layer, which can guide the directional water transport continuously and spontaneously, thus preventing the skin from being rewetted. The resulting trilayered fibrous membranes exhibit a high one-way transport index R (1021%) and a desired breakthrough pressure (16.1 cm H O) in the reverse direction, indicating an ultrahigh directional water transport capacity. Moreover, on the basis of water transport behavior, a plausible mechanism is proposed to provide insight into the integrative and cooperative driving forces at the interfaces of trilayered hydrophobic/transfer/superhydrophilic fibrous membranes. The successful synthesis of such fascinating materials would be valuable for the design of functional textiles with directional water transport properties for personal drying applications.

MicroRNAs are known to regulate gene function in many tissues and organs, but their expression and function, if any, in tooth development are elusive. We sought to identify them by microRNA screening analyses and reveal their overall roles by inactivating Dicer1 in the dental epithelium and mesenchyme. Discrete sets of microRNAs are expressed in molars compared with incisors as well as epithelium compared with mesenchyme. Conditional knockout (cKO) of Dicer1 (mature microRNAs) in the dental epithelium of the Pitx2-Cre mouse results in multiple and branched enamel-free incisors and cuspless molars, and change in incisor patterning and in incisor and molar size and shape. Analyses of differentiating dental epithelial markers reveal a defect in amelo-blast differentiation. Conversely, the cervical loop (stem cell niche) is expanded in Dicer1 cKO. These results demonstrate that tooth development is tightly controlled by microRNAs and that specific microRNAs regulate tooth epithelial stem cell differentiation.