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. 2022 Jul 4;18(11):4357–4371. doi: 10.7150/ijbs.69969

Figure 7.

Figure 7

Selumetinib, a MEK1/2 inhibitor, reversed DUSP4 loss associated Lenvatinib resistance in vivo. (A and B) Both Lenvatinib and Selumetinib could slightly inhibited KO-DUSP4 HCC tumorigenicity. Lenvatinib and Selumetinib combination therapy effectively abolished HCC growth in the nude mice model. (C) The body weights of mice in the three drug-treated groups remained unchanged. Lenvatinib and Selumetinib combination therapy obviously reduced tumor volumes (D) and tumor weights (E). Student's t-test *P < 0.05, **P < 0.01.