YAP/TAZ Pathway Promoted the Trastuzumab Resistance in HER2-Positive Breast Cancer
Wei Wang1, Meifeng Zhou2, Yuebo Liang1, Fan Zhang1, Zhong Wu3, Shaowei Mo4* and Yi Qing Wang1*
1Department of General Surgery, Hainan General Hospital, Hainan Medical University, Haikou, Hainan, China
2Department of Medical Oncology, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University), Haikou 570311, Hainan, China
3Department of General Surgery, Hainan Maternal and Child Health Medical Center, Haikou, Hainan, China.
4Department of Sicience and Education, Hainan Maternal and Child Health Medical Center, Haikou, Hainan, China.
Wei Wang and Meifeng Zhou contributed equally to this article.
Fig. 1.
Expression of YAP in clinical tissues of HER2 positive breast cancer patients. (A) Protein expression of YAP detected by western blotting. (B) Relative mRNA expression of YAP determined using RT-qPCR. ** P<0.01 vs tumor group (Student’s t tests).
Fig. 2.
Expression of YAP/TAZ in vitro. (A) Protein expression of YAP and TAZ detected by western blotting. (B) Relative mRNA expression of YAP and TAZ determined using RT-qPCR. ** P<0.01 vs SK-BR-3-TS group (Student’s t tests).
Fig. 3.
Cell viability was increased while cell apoptosis was inhibited in SK-BR-3-TR cells. (A) Cell viability detected by MTT assay. (B) Cell apoptosis analyzed by flow cytometry. ** P<0.01 vs SK-BR-3-TS group (Student’s t tests).
Fig. 4.
Depletion of YAP reversed the induced trastuzumab resistance in SK-BR-3-TR cells. (A) Protein expression of YAP and TAZ detected by western blotting. (B) Cell apoptosis analyzed by flow cytometry. (C) Cell viability detected by MTT assay. ** P<0.01 vs SK-BR-3-TS group. ## P<0.01 vs SK-BR-3-TR group (One way ANOVA).