摘要
Resistance to chemotherapy is a prominent clinical problem in high grade serous ovarian cancer(HGSOC).1 An inadequate understanding of adaptive signaling coupled with limited treatment options for a chemoresistant tumor are likely causes for poor outcomes.We previously reported that BMI1,a stem-cell factor is instrumental in regulating chemoresistance.2,3 However,to advance anti-BMI1 therapy from the bench to the bedside,efficacy needs to be tested in patient-derived chemoresistant HGSOC models,which is lacking.
基金
This study was supported by research awards from the US Department of Defense to RB(No.W81XWH1810073,and W81XWH1810054)
Histology and immunohistochemistry service was provided by the Stephenson Cancer Tissue Pathology research core supported by the NIGMS Grant P20GM103639 and NCI Grant P30CA225520 of the NIH.
