Fig. 1.

Overexpression of ENO1 and PKM in HBV-Related HCC is associated with patient survival. (A-B) Based on GEPIA database, ENO1 (A) and PKM (B) were highly expressed in HCC tissues than that in adjacent normal tissues. * P < 0.05. ** P < 0.01. *** P < 0.001. (C-D) Analysis of GEPIA database indicated that, high expression of ENO1 (C) and PKM (D) in patients with HCC was associated with shorter overall survival and progression-free survival. (E-F) By analysis of TCGA database with the TIDE analytical tool, high expression of ENO1 (E) and PKM (F) was positively correlated with multiple immune checkpoint genes, including PD1 (CD274), CTLA4, HAVCR2, TIGIT, and CD40. * P < 0.05. ** P < 0.01. *** P < 0.001. **** P < 0.0001. (G) High expression of ENO1 and PKM indicated high TIDE score. **** P < 0.0001. (H-I) By CIBERSORT algorithm, ENO1 (H) and PKM (I) were associated with immune cell infiltration patterns in the tumor microenvironment. * P < 0.05. ** P < 0.01. *** P < 0.001. The symbol “ns” represented differences that were not statistically significant