A total of 14 candidate hub genes most likely to mediate NASH and TNBC occurrence were identified, including TLR4, CYBB, NCF1, NCF2, S100A8, S100A9, ITGB2, RAC2, ITGAM, CYBA, ICAM1, CXCL10, CXCR3, and ITGAL. The gene discussed is CXCR3; the disease is metabolic dysfunction-associated steatohepatitis.