ANP32E induces tumorigenesis of triple-negative breast cancer cells by upregulating E2F1.
Ontology highlight
ABSTRACT: Triple-negative breast cancer (TNBC) lacks expression of estrogen receptor (ER), progesterone receptor, and the HER2 receptor; it is highly proliferative and becomes the deadliest forms of breast cancer. Effective prognostic methods and therapeutic targets for TNBC are required to improve patient outcomes. Here, we report that acidic nuclear phosphoprotein 32 family member E (ANP32E), which promotes cell proliferation in mammalian development, is highly expressed in TNBC cells compared to other types of breast cancer. High expression of ANP32E correlates significantly with worse overall survival (OS; P < 0.001) and higher risks of disease recurrence (P < 0.001) in patients with TNBC. Univariate and multivariate Cox-regression models show that ANP32E is an independent prognostic factor in T
SUBMITTER: Xiong Z
PROVIDER: S-EPMC5983205 | biostudies-literature | 2018 Jun
REPOSITORIES: biostudies-literature
ACCESS DATA