OLFML2A is necessary for anti-triple negative breast cancer effect of selective activator protein‐1 inhibitor T-5224
Triple-negative breast cancer
DOI:
10.1016/j.tranon.2021.101100
Publication Date:
2021-05-13T16:46:07Z
AUTHORS (11)
ABSTRACT
Previous studies have shown that expression of activator protein-1 (AP-1) family is significantly elevated in triple-negative breast cancer (TNBC), compared with other subtypes. Here we investigated the anti-tumor effect and mechanism T-5224, an inhibitor c-Fos/AP-1, on TNBC. We identified T-5224 inhibited proliferation, migration, invasion TNBC cells resulted increase apoptosis. Furthermore, found OLFML2A a key regulatory protein acting downstream AP-1 involved T-5224-targeted action. Multiple clinical databases online high level associated poor prognosis patients. In summary, our experimental bioinformatic indicated necessary for AP-1-overexpressing These findings demonstrate dependent OLFML2A, targeting both through T‐5224 may be synergistic therapeutic strategy this clinically challenging subset cancer.
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