Among patient-derived models, miR-644a was expressed a median of 4.8-fold higher in females compared to males. Our findings implicate miR-644a as a candidate tumor cell-intrinsic regulator of sex-biased gene expression in GBM.
Our findings provide insights into the oncogenic role of BCAR4 and implicate BCAR4 as a potential diagnostic biomarker and a promising therapeutic agent to suppress metastasis and inhibit chemo-resistance of breast cancer.
3 years ago
Journal
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ABCB1 (ATP Binding Cassette Subfamily B Member 1) • CCR7 (Chemokine (C-C motif) receptor 7) • BCAR4 (Breast Cancer Anti-Estrogen Resistance 4) • MIR644A (MicroRNA 644a)
Besides that, inhibition of miR-644a abolished the promoting action of hsa_circ_0007380 knockdown on esophagus cancer apoptosis and radiosensitivity. Hsa_circ_0007380 silencing impedes cell growth and reinforces radiosensitivity in esophagus cancer by miR-644a/SPIN1 axis, suggesting a promising therapeutic target for esophagus cancer combined treatment.