We developed a novel strategy for delivering oncogenic c-Myc inhibitors for targeting melanoma cells. c-Myc prodrugs (PDs) were developed based on Sn-2 phospholipid PDs by coupling 10058-F4 ...
Researchers at Children’s Hospital of Fudan University, Shanghaitech University and Suzhou Zhongke New Drug Incubator Biomedical Technology Co. Ltd. have identified WD repeat-containing protein 5 ...
Heat-shock protein 90 (Hsp90) inhibitor downregulates c-Myc expression and upregulates the expression of tumor repressor proteins such as p53 and pRB, inhibiting the G1/S transition and causing G2 ...
Ubiquitin-specific protease 7 (USP7) is involved in DNA repair and cell cycle progression and, due to its control over the ubiquitination of key proteins, may impact oncogenes like MDM2 and c-Myc, as ...
Activation of MYC is synthetic lethal with IRE1/XBP1 pathway inhibition. We found that inhibition of the IRE1/XBP1 pathway with a highly selective IRE1 RNase inhibitor ORIN1001 suppresses ...
The objectives of the present work were: to develop and characterize an Sn-2 lipase-labile PD of a c-Myc inhibitor; to demonstrate the stability of the c-Myc-PD in the PFC NPs; to demonstrate the ...
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