SETDB2 promoted breast cancer stem cell maintenance by interaction with and stabilization of ΔNp63α protein

SETDB2 通过与 ΔNp63α 蛋白相互作用并稳定其来促进乳腺癌干细胞的维持

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作者:Liu Ying, Xie Fei, Li Jialun, Xiao Jianpeng, Wang Jie, Mei Zhaolin, Fan Hongjia, Fang Huan, Li Sha, Wu Qiuju, Yuan Lin, Liu Cuicui, Peng You, Zhao Weiwei, Wang Lulu, Wong Jiemin, Li Jing, Feng Jing

Abstract

The histone H3K9 methyltransferase SETDB2 is involved in cell cycle dysregulation in acute leukemia and has oncogenic roles in gastric cancer. In our study, we found that SETDB2 plays essential roles in breast cancer stem cell maintenance. Depleted SETDB2 significantly decreased the breast cancer stem cell population and mammosphere formation in vitro and also inhibited breast tumor initiation and growth in vivo. Restoring SETDB2 expression rescued the defect in breast cancer stem cell maintenance. A mechanistic analysis showed that SETDB2 upregulated the transcription of the ΔNp63α downstream Hedgehog pathway gene. SETDB2 also interacted with and methylated ΔNp63α, and stabilized ΔNp63α protein. Restoring ΔNp63α expression rescued the breast cancer stem cell maintenance defect which mediated by SETDB2 knockdown. In conclusion, our study reveals a novel function of SETDB2 in cancer stem cell maintenance in breast cancer.

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