Revitalizing our earth: unleashing the power of green energy in soil remediation for a sustainable future.

This study investigates the feasibility of using renewable energy sources in soil remediation to advance green recovery in a way that is both sustainable and kind to the environment. The report stresses the need to reduce the adverse effects of soil pollution in China and foster economic recovery. This study aims to determine how green energy may be most effectively used in soil remediation operations.

Down-regulation of CASC2 contributes to cisplatin resistance in gastric cancer by sponging miR-19a.

Increasing evidence suggests the involvement of long non-coding RNAs (lncRNAs) in chemoresistance of cancer treatment. However, their function and molecular mechanisms in gastric cancer chemoresistance are still not well elucidated. In the present study, we investigate the functional role of lncRNA cancer susceptibility candidate 2 (CASC2) in cisplatin (DDP) resistance of gastric cancer and discover the underlying molecular mechanism.

Effects of Acupuncture on 1-chloro-2,4-dinitrochlorobenzene-induced Allergic Contact Dermatitis in Mice.

Allergic contact dermatitis (ACD) is a chronic inflammatory skin disease. Topical corticosteroids are the first-line therapy for ACD despite their significant adverse effects. Acupuncture has been widely used in the treatment of various skin diseases, but its underlying mechanism remains unrevealed.

EphB3-targeted regulation of miR-149 in the migration and invasion of human colonic carcinoma HCT116 and SW620 cells.

microRNAs play key roles during various crucial cell processes such as proliferation, migration, invasion and apoptosis. Also, microRNAs have been shown to possess oncogenic and tumor-suppressive functions in human cancers. Here, we describe the regulation and function of miR-149 in colorectal cancer cell lines.

[Development and effectiveness evaluation of time-resolved fluoroimmunoassay kit for detection of ].

Objective: To develop a kit of time-resolved fluoroimmunoassay (TRFIA) for detection of protein SjP38, and evaluate its effectiveness.

Methods: The anti 9G7 SjP38 monoclonal antibody was used as the capture anti-body coated with 96-hole plate, and the Eu3 labeled 1A6 monoclonal antibody was used as the detection antibody to establish the TRFIA SjP38 kit. In addition, the accuracy, sensitivity, precision, stability and coincidence rate to pathogenic diagnosis of the kit were evaluated.