RETRACTED: Allosteric Activators of Protein Phosphatase 2A Display Broad Antitumor Activity Mediated by Dephosphorylation of MYBL2

• Published in: Cell 2020-04, Vol.181 (3), p.702-715.e20
• Main Authors: Morita, Ken, He, Shuning, Nowak, Radosław P., Wang, Jinhua, Zimmerman, Mark W., Fu, Cong, Durbin, Adam D., Martel, Megan W., Prutsch, Nicole, Gray, Nathanael S., Fischer, Eric S., Look, A. Thomas
• Format: Article
• Language: English
• Subjects: Apoptosis; Cell Cycle Proteins - drug effects; Cell Cycle Proteins - metabolism; Cell Line, Tumor; Enzyme Activators - metabolism; G1 Phase; Humans; Multiprotein Complexes - metabolism; Multiprotein Complexes - physiology; Phenothiazines - pharmacology; Phosphorylation; Protein Phosphatase 2 - metabolism; Protein Phosphatase 2 - physiology; Protein Subunits - metabolism; Trans-Activators - drug effects; Trans-Activators - metabolism; Transcription Factors - metabolism
• ISSN: 0092-8674; 1097-4172
• DOI: 10.1016/j.cell.2020.03.051

This article has been retracted: please see Elsevier Policy on Article Withdrawal (https://www.elsevier.com/about/our-business/policies/article-withdrawal). This article has been retracted at the request of the authors. Their study showed that different PP2A holoenzymes, composed of distinct subunits and acting on unique substrates, can be specifically targeted by different small-molecule allosteric activators, including perphenazine. An important part of the study was the identification of a compound the authors called iHAP1 (improved heterocyclic activator of PP2A) that was suitable for in vivo studies in zebrafish and murine models because it did not interfere with dopamine signaling, which caused dose limiting off-target toxicity in the case of perphenazine. The authors also assessed iHAP1 for a second type of off-target activity involving inhibition of tubulin polymerization, and they reported that iHAP1 did not affect tubulin polymerization into microtubules (Figures S6D and S6E). Recently, Vit and coworkers published an article in The EMBO Journal showing that iHAP1 does in fact significantly inhibit tubulin polymerization (Vit et al., 2022, EMBO J. 41, e110611, https://doi.org/10.15252/embj.2022110611). The authors have subsequently used the same tubulin polymerization kit that they originally used for determining the effects of small molecules on the rate of tubulin polymerization and carefully optimized the conditions with the control compounds provided with the kit. After recalibration of the plate reader based on these controls, the authors determined that their original results are not reproducible and that iHAP1 does in fact potently inhibit tubulin polymerization. They are uncertain why their original analysis yielded inaccurate results. Unfortunately, the fact that iHAP1 inhibits tubulin polymerization renders uninterpretable their in vivo studies showing anti-cancer cell activity in zebrafish and murine models, because they cannot tell how much of the activity is due to activation of PP2A and how much is contributed by the anti-tubulin activities of this molecule. Because these in vivo studies and other in vitro studies in the paper prominently include iHAP1, all of the authors have agreed that the most appropriate course of action is to retract the paper. Many in vitro experiments in the paper that address different aspects of PP2A activation were performed with both iHAP1 and perphenazine, which does not possess detectable anti-tubulin a