Search

C/SiC composite has been widely used as a high‐temperature material for engineering components due to its excellent thermal properties. Facing the rapid development and threat of high‐energy laser, study on the ablation resistance under laser irradiation is strongly required. In this work, a continuous high‐energy laser was applied to explore the laser ablation behavior and mechanism of C/SiC composite. From the results, C/SiC composite shows different morphologies when irradiated at various laser power densities for 500 and 700 W/cm2. We divided the ablation area into three regions; the central, transition, and edge regions, where the formation of SiO2, SiO, and the breakage of carbon fiber were observed. The generated highly reflective SiO2 layer reduces the absorption of laser energy, which is beneficial to lower the back‐surface temperature and reduce the damage of composite. In addition, we put forward the ablation physical models and ablation mechanisms irradiated at different power densities. The work provides a basis for the laser ablation resistance of C/SiC composites under different conditions. [ABSTRACT FROM AUTHOR]

Millireactors are widely used in flow chemistry due to their process intensification performance and sufficient product throughout. A novel structured tube‐in‐tube millireactor with industrial potential was designed, whose mixing and heat transfer were investigated by experiment and CFD. Partial least square regression (PLS) was introduced in the flow chemistry study and used to determine that the key parameters of the millireactor were jet Reynolds (Reh) and hole diameter Dh. The introduction of twist tape in the annular space generates swirling flow, which effectively increases the heat transfer capacity (up to 16.5 times). This millireactor achieves excellent mixing (>99% of mixing intensity after 1 cm) and the heat transfer enhancement ratio up to 6.5. The local flow field and concentration field from CFD model agreed with those obtained from PIV and PLIF visualization experiments. [ABSTRACT FROM AUTHOR]

Pancreatic cancer (PC) is one of the most deadly digestive cancers world‐wide, with a dismal five‐year survival rate of <8%. Upregulation of transmembrane protein 158 (TMEM158) is known to facilitate the progression of several carcinomas. However, little is known concerning the potential roles of TMEM158 in PC. Herein, we first found that TMEM158 was significantly upregulated in PC samples as well as PC cell lines. The overexpression of TMEM158 was significantly correlated with advanced clinicopathologic features (including tumor size, TNM stage, and blood vessel invasion) and poorer prognosis of patients with PC in clinic. Evidenced based on a series of loss‐ and gain‐of‐function assays uncovered that TMEM158 enhanced PC cell proliferation, migration, and invasion by stimulating the progression of cell cycle, epithelial–mesenchymal transition, and MMP‐2/9 production. Furthermore, mechanism‐related investigations disclosed that activation of TGFβ1 and PI3K/AKT signal might be responsible for TMEM158‐triggered PC aggressiveness. Collectively, TMEM158 was upregulated in PC and promoted PC cell proliferation, migration, and invasion through the activation of TGFβ1 and PI3K/AKT signaling pathways, highlighting its potential as a tumor promoter and a therapeutic target for PC. [ABSTRACT FROM AUTHOR]

The human secretome and membrane proteome are a large source of cancer biomarkers. Membrane-bound and secreted proteins are promising targets for many clinically approved drugs, including for the treatment of tumours. Here, we report a deep systematic analysis of 957 adenocarcinomas of the oesophagus, stomach, colon and rectum to examine the cancer-associated human secretome and membrane proteome of gastrointestinal tract adenocarcinomas (GIACs). Transcriptomic data from these GIACs were applied to an innovative majority decision-based algorithm. We quantified significantly expressed protein-coding genes. Interestingly, we found a consistent pattern in a small group of genes found to be overexpressed in GIACs, which were associated with a cytokine-cytokine interaction pathway (CCRI) in all four cancer subtypes. These CCRI associated genes, which spanned both one secretory and one membrane isoform were further analysed, revealing a putative biomarker, interleukin-1 receptor accessory protein (IL1RAP), which indicated a poor overall survival, a positive correlation with cancer stemness and a negative correlation with several kinds of T cells. These results were further validated in vitro through the knockdown of IL1RAP in two human gastric carcinoma cell lines, which resulted in a reduced indication of cellular proliferation, migration and markers of invasiveness. Following IL1RAP silencing, RNA seq results showed a consistent pattern of inhibition related to CCRI, proliferation pathways and low infiltration of regulatory T cells (Tregs) and CD8 naive cells. The significance of the human secretome and membrane proteome is elucidated by these findings, which indicate IL1RAP as a potential candidate biomarker for cytokine-mediated cancer immunotherapy in gastric carcinoma., (© 2022 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.)