Ferroptosis is an iron-dependent form of regulated cell death characterized by lipid peroxidation. Colorectal cancer (CRC) cells evade ferroptosis despite their requirement of substantial iron and reactive oxygen species (ROS) to sustain active metabolism and extensive proliferation. However, the underlying mechanism is unclear. Herein, we report the role of lymphoid-specific helicase (LSH), a chromatin-remodeling protein, in suppressing erastin-induced ferroptosis in CRC cells. We demonstrate that erastin treatment leads to dose- and time-dependent downregulation of LSH in CRC cells, and depletion of LSH increases cell sensitivity to ferroptosis. Mechanistically, LSH interacts with and is stabilized by ubiquitin-specific protease 11 (USP11) via deubiquitination; this interaction was disrupted by erastin treatment, resulting in increased ubiquitination and LSH degradation. Moreover, we identified cytochrome P450 family 24 subfamily A member 1 (CYP24A1) as a transcriptional target of LSH. LSH binds to the CYP24A1 promoter, promoting nucleosome eviction and reducing H3K27me3 occupancy, thus leading to transcription of CYP24A1. This cascade inhibits excessive intracellular Ca2+ influx, thereby reducing lipid peroxidation and ultimately conferring resistance to ferroptosis. Importantly, aberrant expression of USP11, LSH, and CYP24A1 is observed in CRC tissues and correlates with poor patient prognosis. Taken together, our study demonstrates the crucial role of the USP11/LSH/CYP24A1 signaling axis in inhibiting ferroptosis in CRC, highlighting its potential as a therapeutic target in CRC treatment.

Utilizing sintered ore catalysts (SOC), which are used in the sintering industry for NH3-SCR denitration, is a feasible and economical way to reduce NOx emission in sintering flue gas. Therefore, in order to enhance the denitration efficiency of SOC, sintered ore modified by sulfuric acid and sulfated sintered ore catalysts (SSOC-5) were prepared. Kinetic analyses of these two catalysts for denitration were carried out in this study. On the basis of eliminating the influence of internal and external diffusion, the relationship between reactants and reaction rate was studied by a power function kinetic model. This clarified that the adsorption ability of the acid-modified catalyst for reaction gas adsorption was stronger than that of sintered ore catalysts, and the reaction rate was also accelerated. The NO, NH3 and O2 reaction orders of SOC were 1, 0.3 and 0.16 at 250~300 °C, while these values of SSOC-5 were 0.8, 0.06 and 0.09, respectively. The apparent activation energy of SOC was 83.66 kJ/mol, while the value of SSOC-5 decreased to 59.93 kJ/mol.