MD-222 is a First-in-Class Highly Potent PROTAC Degrader of MDM2

PROTACs are heterobifunctional molecules that connect a POI ligand to an E3 ubiquitin ligase recruiting ligand with an optimal linker. Researchers reported the discovery of MD-222. MD-222 is the first-in-class highly potent PROTAC degrader of MDM2.

MD-222 induces rapid degradation of the MDM2 protein and activation of wild-type p53 in cells. Moreover, MD-222 potently inhibits cell growth in human cancer cell lines carrying wild-type p53. MD-222 potently and effectively inhibits cell growth in each of these three leukemia cell lines and is much more potent than their corresponding MDM2 inhibitors. MD-222 displays a high cellular specificity over cancer cell lines carrying mutated or deleted p53. Furthermore, MD-222 is very effective in reducing the levels of MDM2 protein and increasing the levels of p53. Treatment of the RS4;11 cells with MD-222 reduces the level of MDM2 and increases the level of p53.

MD 222 is a First in Class Highly Potent PROTAC Degrader of MDM2 2021 05 14 - MD-222 is a First-in-Class Highly Potent PROTAC Degrader of MDM2

MD-222 can reduce the levels of MDM2 in the RS4;11/IRMI-2 cell line carrying a mutated p53. MD-222 is effective in reducing the levels of MDM2 and activating wild-type p53 in RS4;11 cells. Treatment of the RS4;11 cells with MD-222 effectively induces depletion of MDM2 protein and currently accumulation of p53 protein in a dose-dependent manner. MD-222 is potent and effective in inducing depletion of MDM2 protein and accumulation of p53 protein in MV4;11 cell line, when compared to RS4;11 cell line.

Together, MD-222 is highly effective and potent in induction of MDM2 degradation and accumulation of p53 in both RS4;11 and MV4;11 cell lines.

Reference:
Jiuling Yang, et al. Simple Structural Modifications Converting a Bona fide MDM2 PROTAC Degrader into a Molecular Glue Molecule: A Cautionary Tale in the Design of PROTAC Degraders. J Med Chem. 2019 Nov 14;62(21):9471-9487.

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