METTL3 is known to be involved in all stages in the life cycle of RNA. It affects the tumor formation by the regulation the m6A modification in the mRNAs of critical oncogenes or tumor suppressors. ...In bladder cancer, METTL3 could promote the bladder cancer progression via AFF4/NF-κB/MYC signaling network by an m6A dependent manner. Recently, METTL3 was also found to affect the m6A modification in non-coding RNAs including miRNAs, lincRNAs and circRNAs. However, whether this mechanism is related to the proliferation of tumors induced by METTL3 is not reported yet.
Quantitative real-time PCR, western blot and immunohistochemistry were used to detect the expression of METTL3 in bladder cancer. The survival analysis was adopted to explore the association between METTL3 expression and the prognosis of bladder cancer. Bladder cancer cells were stably transfected with lentivirus and cell proliferation and cell cycle, as well as tumorigenesis in nude mice were performed to assess the effect of METTL3 in bladder cancer. RNA immunoprecipitation (RIP), co-immunoprecipitations and RNA m6A dot blot assays were conducted to confirm that METTL3 interacted with the microprocessor protein DGCR8 and modulated the pri-miR221/222 process in an m6A-dependent manner. Luciferase reporter assay was employed to identify the direct binding sites of miR221/222 with PTEN. Colony formation assay and CCK8 assays were conducted to confirm the function of miR-221/222 in METTL3-induced cell growth in bladder cancer.
We confirmed the oncogenic role of METTL3 in bladder cancer by accelerating the maturation of pri-miR221/222, resulting in the reduction of PTEN, which ultimately leads to the proliferation of bladder cancer. Moreover, we found that METTL3 was significantly increased in bladder cancer and correlated with poor prognosis of bladder cancer patients.
Our findings suggested that METTL3 may have an oncogenic role in bladder cancer through interacting with the microprocessor protein DGCR8 and positively modulating the pri-miR221/222 process in an m6A-dependent manner. To our knowledge, this is the first comprehensive study that METTL3 affected the tumor formation by the regulation the m6A modification in non-coding RNAs, which might provide fresh insights into bladder cancer therapy.
Ultrathick electrode design is a promising strategy to enhance the specific energy of Li‐ion batteries (LIBs) without changing the underlying materials chemistry. However, the low Li‐ion conductivity ...caused by ultralong Li‐ion transport pathway in traditional random microstructured electrode heavily deteriorates the rate performance of ultrathick electrodes. Herein, inspired by the vertical microchannels in natural wood as the highway for water transport, the microstructures of wood are successfully duplicated into ultrathick bulk LiCoO2 (LCO) cathode via a sol–gel process to achieve the high areal capacity and excellent rate capability. The X‐ray‐based microtomography demonstrates that the uniform microchannels are built up throughout the whole wood‐templated LCO cathode bringing in 1.5 times lower of tortuosity and ≈2 times higher of Li‐ion conductivity compared to that of random structured LCO cathode. The fabricated wood‐inspired LCO cathode delivers high areal capacity up to 22.7 mAh cm−2 (five times of the existing electrode) and achieves the dynamic stress test at such high areal capacity for the first time. The reported wood‐inspired design will open a new avenue to adopt natural hierarchical structures to improve the performance of LIBs.
Inspired by the vertical microchannels in natural wood as the highway for water transport, an ultra‐thick bulk LiCoO2 (LCO) cathode with vertical channels is fabricated to enhance the transport of Li+. Remarkably, the fabricated LCO cathode shows low tortuosity and high Li‐ion conductivity, and can deliver high areal capacity up to 22.7 mAh cm−2.
Effective capture of radioactive iodine is of paramount importance for the safe and long‐term storage of fission products in the nuclear fuel cycle. Herein, a series of functionalized Th‐UiO‐66 MOFs ...was employed as a model to investigate the effects of substituents on iodine adsorption in both solution and vapor states. Sorption studies revealed that the electro‐donating amino group exhibits the most positive role on increasing the removal rate of iodine from cyclohexane and the uptake capacity of iodine vapor. Particularly, the disubstituted Th‐UiO‐66‐(NH2)2 can effectively remove 91.9 % of iodine (300 mg L−1) from cyclohexane and capture 969 mg g−1 iodine vapor, significantly higher than 59.6 % and 334 mg g−1 of untagged Th‐UiO‐66, respectively. In addition, the substituent effect on the radiolytic stability of MOFs was for the first time investigated, leading to the unearthing of one of the most radioresistant MOFs Th‐UiO‐66‐NH2 reported to date.
A systematic study on the effects of aromatic substitution on iodine adsorption was performed by employing Th‐UiO‐66 as a platform, giving rise to the disubstituted Th‐UiO‐66‐(NH2)2 with the best iodine sorption performance. Moreover, aromatic substitution was employed as a new strategy to enhance the radioresistance of MOFs.
Radiation dosimeters displaying conspicuous response of irradiance are highly desirable, owing to the growing demand of monitoring high-energy radiation and environmental exposure. Herein, we present ...a case of dosimetry based on a discrete nanocluster, Th
(OH)
(O)
(H
O)
(TPC)
(HCOO)
∙4DMF∙H
O (Th-SINAP-100), by judiciously incorporating heavy Th
polynuclear centers as radiation attenuator and organic linkers as photo-responsive sensor. Interestingly, dual-module photochromic transitions upon multiple external stimuli including UV, β-ray, and γ-ray are integrated into this single material. The striking color change, and more significantly, the visible color transition of luminescence in response to accumulating radiation dose allow an on-site quantitative platform for naked-eye detection of ionization radiations over a broad range (1-80 kGy). Single crystal X-ray diffraction and density functional theory calculations reveal that the dual-module photochromism can be attributed to the π(TPC) → π*(TPC) intermolecular charge transfer driven by enhanced π-π stacking interaction between the adjacent TPC moieties upon irradiation.
A nanotubular metal−organic framework (MOF), {(WS4Cu4)I2(dptz)3·DMF} n (dptz = 3,6-di(pyridin-4-yl)-1,2,4,5-tetrazine, DMF = N,N-dimethylformamide) for sensing small solvent molecules is presented. ...When accommodating different solvent molecules as guests, the resulting inclusion compounds exhibit different colors depending on the solvent guests, and more interestingly, the band gaps of these solvent-included complexes are in linear correlation with the polarity of the guest solvents. The solvent molecules can be sensed by the changes of UV−vis spectra of the corresponding inclusion compounds, showing a new way of signal transduction as a new kind of sensor. The sensing by such a MOF occurs within the channel-containing material rather than on the external surface.
A palladium‐catalyzed oxidative amidation of conjugated olefin with 2‐pyridone is described. A series of E‐Enamides were synthesized in a highly stereocontrolled manner. The reaction also ...accommodates other cyclic and acyclic amides. Z‐Enamides were predominantly prepared for primary amides probably due to the presence of an intramolecular hydrogen bond. Gram‐scale synthesis of enamide and the following oxidative annulation with diphenylacetylene demonstrates the synthetic utility of this reaction.
Palladium‐catalyzed oxidative amidation of conjugated olefin with 2‐pyridone is developed. A series of E‐Enamides were synthesized with high stereoselectivities. Other cyclic and acyclic amides are also tolerated in this catalytic system.
This perspective highlights the recent advances in the structural and practical aspects of thorium-based metal-organic frameworks (Th-MOFs) and molecular clusters. Thorium, as an underexplored ...actinide, features surprisingly rich coordination geometries and accessibility of the 5f orbital. These features lead to a myriad of topologies and electronic structures, many of which are undocumented for other tetravalent metal-containing MOFs or clusters. Moreover, Th-MOFs inherit the modularity, structural tunability, porosity, and versatile functionality of the state-of-the-art MOFs. Recognizing the radioactive nature of these thorium-bearing materials that may limit their practical uses, Th-MOFs and Th-clusters still have great potential for various applications, including radionuclide sequestration, hydrocarbon storage/separation, radiation detection, photoswitch, CO
2
conversion, photocatalysis, and electrocatalysis. The objective of this updated perspective is to propose pathways for the renaissance of interest in thorium-based materials.
This perspective summarizes the recent advances in the structures and applications of thorium-based metal-organic frameworks and molecular clusters.
The vortex, a fundamental topological excitation featuring the in-plane winding of a vector field, is important in various areas such as fluid dynamics, liquid crystals, and superconductors. Although ...commonly existing in nature, vortices were observed exclusively in real space. Here, we experimentally observed momentum-space vortices as the winding of far-field polarization vectors in the first Brillouin zone of periodic plasmonic structures. Using homemade polarization-resolved momentum-space imaging spectroscopy, we mapped out the dispersion, lifetime, and polarization of all radiative states at the visible wavelengths. The momentum-space vortices were experimentally identified by their winding patterns in the polarization-resolved isofrequency contours and their diverging radiative quality factors. Such polarization vortices can exist robustly on any periodic systems of vectorial fields, while they are not captured by the existing topological band theory developed for scalar fields. Our work provides a new way for designing high-Q plasmonic resonances, generating vector beams, and studying topological photonics in the momentum space.
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As a new and important technology in architecture, engineering, and construction (AEC), Building Information Modeling (BIM) has witnessed a decade of rapid development. It is highly necessary to ...analyze the research progress and development trend of BIM. Based on 1369 relevant literatures published and the core database “Web of Science”, this study used co-citation analysis, co-word analysis, and cluster analysis to analyze the data and drew the mapping knowledge domains with Citespace software. The results show that BIM research is still in the rapid growth stage. And BIM research is mainly distributed in nine fields. In terms of time sequence, the development of BIM in the past decade developed from data collection to information integration and to knowledge management. The research hotspots are mainly concentrated in eleven directions, which can be further classified into three levels. This paper will provide valuable theoretical and practical reference for the future research of BIM.
•Co-citation analysis, co-word analysis, and cluster analysis are used to draw the mapping knowledge domains.•BIM research is mainly distributed in nine fields that constitute the intellectual base of BIM research.•Research hotspots of BIM are mainly concentrated in the eleven directions.•The eleven directions of BIM research are classified into three levels.
Polymorphism control of metal‐organic frameworks is highly desired for elucidating structure‐property relationships, but remains an empirical process and is usually done in a trial‐and‐error ...approach. We adopted the rarely used actinide cation Th4+ and a ditopic linker to construct a series of thorium‐organic frameworks (TOFs) with a range of polymorphs. The extraordinary coordination versatility of Th4+ cations and clusters, coupled with synthetic modulation, gives five distinct phases, wherein the highest degree of interpenetration (threefold) and porosity (75.9 %) of TOFs have been achieved. Notably, the O atom on the capping site of the nine‐coordinated Th4+ cation can function as a bridging unit to interconnect neighboring secondary building units (SBUs), affording topologies that are undocumented for other tetravalent‐metal‐containing MOFs. Furthermore, for the first time HCOOH has been demonstrated as a bridging unit of SBUs to further induce structural complexity. The resulting TOFs exhibit considerably different adsorption behaviors toward organic dyes, thus suggesting that TOFs represent an exceptional and promising platform for structure‐property relationship study.
The extraordinary coordination versatility of Th4+ cation and the unexpected bridging role of formate allow polymorphism control of thorium‐organic frameworks (TOFs) with five distinct phases, wherein the highest degree of interpenetration and porosity for TOFs have been achieved. The resulting TOFs exhibit considerably different adsorption behaviors toward organic dyes, thus suggesting that TOFs represent an excellent platform for structure‐property relationship study.
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