Ontology highlight
ABSTRACT: Background
Colorectal cancer (CRC) is a leading cause of cancer-related deaths, with metabolic reprogramming involved in its pathogenesis. Aberrant Arginase 2 (ARG2) expression is linked to malignant progression, but its role in CRC remains unclear.Methods
ARG2 expression in CRC and adjacent tissues was analyzed. In vitro experiments were performed after ARG2 knockdown. Mechanistic investigations focused on epithelial-mesenchymal transition (EMT), PI3K/AKT pathway, immune infiltration, and drug sensitivity.Results
ARG2 was upregulated in CRC tissues, correlating with poor prognosis. ARG2 knockdown inhibited CRC cell proliferation, migration, and invasion by reducing Zinc Finger E-Box Binding Homeobox 1 (ZEB1), N-cadherin, and MMP2, suppressing EMT. Additionally, ARG
SUBMITTER: Zhang Y
PROVIDER: S-EPMC12868387 | biostudies-literature | 2026 Feb
REPOSITORIES: biostudies-literature