Inactive von Hippel-Lindau (VHL) is linked to metabolic reprogramming and plays pivotal roles in the pathogenesis of clear cell renal cell carcinoma (ccRCC). Here, we identify a previously unknown oncogenic role for inactive VHL in actively triggering histone lactylation to promote ccRCC progression. In patients with ccRCC, inactive VHL positively correlates with the presence of histone lactylation, and high levels of histone lactylation indicates poor patient prognosis. Inactive VHL-triggered histone lactylation contributes to ccRCC progression by activating the transcription of platelet-derived growth factor receptor β (PDGFRβ). In turn, PDGFRβ signaling is shown to stimulate histone lactylation, thereby forming an oncogenic positive feedback loop in ccRCC. Target correction of aberrant histone lactylation represses the growth and metastasis of ccRCC in vivo. More importantly, the combined inhibition of histone lactylation and PDGFRβ significantly reinforces the therapeutic efficacy. This work underscores the importance of histone lactylation in facilitating ccRCC progression and suggests targeting the positive feedback loop between histone lactylation and PDGFRβ signaling might provide a promising therapeutic strategy for ccRCC patients.

This paper aims to investigate the tribo-mechanical behavior of natural fiber reinforced plastic (NFRP) composites with specific consideration of the multiscale complex structure of natural fibers. Understanding the multiscale tribo-mechanical performances of these eco-friendly materials can lead to a better design of their manufacturing processes. Nanoindentation and nanoscratching experiments are conducted on flax fibers reinforced polypropylene composites using a triboindenter at a specific contact scale generated by the tip indenter radius (100 nm). Results confirm the significant effect of the geometric contact scale on the flax fibers stiffness. Moreover, flax fibers friction shows a multiscale behavior where the mechanisms of nano-friction are vastly different from those of micro-friction, which is related to the physical phenomena arisen at each scale.

Here, we demonstrate the assembly of a new stable lanthanide-based metal-organic framework (MOF), Eu(HDPB)(phen) (1) (HDPB = (1,1ʹ:3ʹ,1ʹʹ-terphenyl)-3,3ʹʹ,5,5ʹʹ-tetracarboxylic acid, phen = 1,10-phenanthroline), with a three-dimensional framework under solvothermal conditions. 1...

This study obtained solution-tractable anion-selective membranes with intrinsic porous and highly ionic conductive capabilities by a convenient route. We used the coplanar structure of 9,9-dimethylxanthene to construct a rigid twisted intrinsic microporous all-carbon skeleton PDI with up to 363.4 m 2 g −1 of Brunauer−Emmett−Teller surface, and the pore was filled with a quaternary ammonium salt containing long flexible alkyl chains, which produced an efficient means of OH − transport. The conductivity of the resulting polymer (QPDI-100) is reached as high as 205 mS cm −1 at 80 °C. The size stability was determined to be good at high conductance and swelling ratio is less than 15% at 80 °C. QPDI-a exhibited good stability under alkaline conditions, and 90% of the conductivity of QPDI-100 was retained after being immersed in 1 M NaOH solution at 60 °C for 40 days. The power density of H 2 −O 2 fuel cells at 60 °C was 437.7 mW cm −2 . The prepared intrinsic porous anion exchange membranes (AEMs) demonstrate potential for the development of anion exchange membrane fuel cells. This membrane design strategy paves the way for a new generation of AEMs for the purposes of electrochemical energy conversion and storage.

Main-chain non-ether anion-exchange membranes (AEMs) have become a research hotspot in recent years because of their ease of preparation and excellent alkaline stability. However, owing to the limitations of the types of monomers and polymerization mechanisms, preparing main-chain non-ether AEMs with controllable morphology remains challenging. Herein, seven poly(fluorene alkylene) membranes, including random and block-structured membranes with different quaternary ammonium (QA) group distributions on the side chains, with the same ion-exchange capacity (IEC) were designed via superacid-catalyzed polymerization. The properties of the as-synthesized membranes were characterized, and the water-transport mechanism has been discussed in relation to the morphology of the membranes. The formed bicontinuous phase structure based on block biphenyl units possessed multidirectional ion channels and distinct ion clusters favorable to water molecule movement. The conductivity of the optimized membrane with a block biphenyl structure reached 208 mS cm–1 at 80 °C, and the peak power density of an H2/O2 fuel cell based on the as-prepared membrane was 0.92 W cm–2. The reported approach is effective in balancing the content of free and bound water within the membrane, generating maximum hydroxide mobility and water transport suitable for high-performance AEM fuel cells. This study highlights the significance of regulating the block structure and adjusting the segment distribution in AEMs to tune their morphologies and provides an innovative design approach for constructing high-performance AEMs.