契约
转移
乳腺癌
癌症研究
相扑蛋白
RAC1
生物
化疗
癌症
肿瘤科
紫杉醇
内科学
医学
信号转导
基因
泛素
生物化学
考古
历史
作者
Luyao Wei,Wantao Wang,Junxia Yao,Zhengyu Cui,Zihang Xu,Hanqing Ding,Xiaojun Wu,Deheng Wang,Jia Luo,Zunji Ke
出处
期刊:Oncogene
[Springer Nature]
日期:2022-08-16
卷期号:41 (37): 4282-4294
被引量:6
标识
DOI:10.1038/s41388-022-02431-6
摘要
Most basal-like breast cancers (BLBCs) are triple-negative breast cancers (TNBCs), which is associated with high malignancy, high rate of recurrence and distant metastasis, and poor prognosis among all types of breast cancer. However, there are currently no effective therapies for BLBC. Furthermore, chemoresistance limits the therapeutic options for BLBC treatment. In this study, we screen out protein activator of the interferon-induced protein kinase (PACT) as an essential gene in BLBC metastasis. We find that high PACT expression level was associated with poor prognosis among BLBC patients. In vivo and in vitro investigations indicated that PACT could regulate BLBC metastasis by interacting with SUMO-conjugating enzyme Ubc9 to stimulate the SUMOylation and thus consequently the activation of Rac1. BLBC patients receiving chemotherapy presents poorer prognosis with PACT high expression, and PACT disruption sensitizes experimental mammary tumor metastases to chemotherapy, thus providing insights to consider PACT as a potential therapeutic target to overcome acquired chemoresistance in BLBC.
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