Fig. 1: ARIH1 accumulates after treatment of 4T1 tumor models with a combination of cisplatin and anti-PD-L1 antibody. | Nature Communications

Fig. 1: ARIH1 accumulates after treatment of 4T1 tumor models with a combination of cisplatin and anti-PD-L1 antibody.

From: ARIH1 activates STING-mediated T-cell activation and sensitizes tumors to immune checkpoint blockade

Fig. 1

a, b Tumor growth curves and tumor weights upon subcutaneous injection of 5 × 105 4T1 cells into female BALB/c mice (6–8 week old) treated with vehicle, cisplatin alone, anti-PD-L1 alone and cisplatin+anti-PD-L1. n = 6 mice/group. Data represent means ± SEM. a **P < 0.01 (P = 0.0052), ****P < 0.0001. b **P < 0.01 (P = 0.0014), ***P < 0.001 (P = 0.0007), ****P < 0.0001. c The survival curves of tumor bearing mice with indicated treatments. n = 7 mice/group. Log-rank test, *P < 0.05 (P = 0.0351), **P < 0.01 (P = 0.0023). d, e. Representative images of tumor CD8 and GzmB IHC staining of the mice as in (a). The percent of each expression pattern was quantified (e). Scale bar, 60 μm. n = 6 mice/group. Data represent means ± SEM, ***P < 0.001 (P = 0.0002), ****P < 0.0001. f Representative ARIH1 IHC staining for tumors of the mice as in (a). The percent of expression pattern was quantified. Scale bar, 60 μm. n = 6 mice/group. Data represent means ± SEM, *P < 0.05 (P = 0.0233). g Immunoblots analysis of the ARIH1 protein levels in the indicated tumor lysates of mice as in (a). h–j Tumor growth, final tumor image and tumor weights of Ctrl-KD and Arih1-KD 4T1 cells in female BALB/c mice (n = 7 per group, 6–8 week old) with indicated treatments. Data represent means ± SEM. h **P < 0.01, ****P < 0.0001. j *P < 0.05, ****P < 0.0001, ns, not significant. Data shown in a and h are representative of three independent experiments. For a, h data, Two-way ANOVA test. For b, e, j data, One-way ANOVA test. For f data, Two-tailed t-test. Source data are provided as a Source Data file.

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