Flexible pressure sensors are currently at the center stage of wearable electronics. Despite tremendous progress in the recent years, flexible pressure sensors with high sensitivity, high stability, and mechanical robustness are still challenging. In this paper, as inspired by the bean pod structure, a sensor architecture consisting a microspacer core layer of polystyrene (PS) microspheres, sandwiched between two laser-induced graphene/polyurethane (LIG/PU) films, is presented. A flexible and self-healable pressure sensor is prepared, achieving ultrahigh sensitivity, improved linearity, wide sensing range up to 100 kPa, and excellent stability (for over 1000 loading−unloading cycles). Specifically, the pressure sensor achieves high sensitivities of 149, 659, and 2048 kPa −1 for the pressure ranges of 0−1, 1−10, and 10−100 kPa, respectively. Upon three cut−heal cycles at room temperature, severely damaged devices are self-healed and are able to maintain high sensitivity. The sensors have been further verified in stringent applications, such as human arterial pulse monitoring and gait detection. The novel device architecture enabling facile fabrication and high performance paves the way to the scalable production of pressure sensors for human physiological diagnostics and other advanced wearable applications.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
The serine protease inhibitor clade E member 1 (SERPINE1) is a major inhibitor of tissue plasminogen activator and urokinase, and has been implicated in the development and progression of a variety of tumors. In this study, mRNA microarray and TCGA database were used to comprehensively analyze the upregulation of SERPINE1 in gastric cancer (GC) tissues compared with the normal stomach tissues. Kaplan-Meier results confirmed that patients with high SERPINE1 expression exhibited worse overall survival and disease-free survival. In addition, cell proliferation, cell scratches, transwell migration and invasion assay showed that SERPINE1 knockdown inhibited the proliferation, migration and invasion of GC ells. Western blot showed that the expression of VEGF and IL-6 was significantly upregulated after overexpression of SERPINE1. Meanwhile, SERPINE1 was positively correlated with the level of immune infiltration using the online analysis tools TISIDB and TIMER. And SERPINE1 expression increased with the increase of malignancy of GC which were detected by Immunohistochemistry. Finally, tumorigenesis experiments in nude mice further demonstrated that SERPINE1 could promote the occurrence and development of GC, while deletion of SERPINE1 inhibited the progression of GC. In summary, SERPINE1 was highly expressed in GC tissues, and SERPINE1 was helpful for differential diagnosis of pathological grade of gastric mucosal lesions. SERPINE1 might regulate the expression of VEGF and IL-6 through the VEGF signaling pathway and JAK-STAT3 inflammatory signaling pathway, thus ultimately affecting the invasion and migration of GC cells.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.