| Literature DB >> 32071079 |
Otto Kauko1,2,3, Susumu Y Imanishi1, Evgeny Kulesskiy4, Laxman Yetukuri1, Teemu Daniel Laajala4,5, Mukund Sharma1,2,3, Karolina Pavic1, Anna Aakula1, Christian Rupp1, Mikael Jumppanen1, Pekka Haapaniemi1, Luyao Ruan6, Bhagwan Yadav4, Veronika Suni1, Taru Varila1, Garry L Corthals1, Jüri Reimand6,7, Krister Wennerberg4, Tero Aittokallio4,5, Jukka Westermarck8,2.
Abstract
Protein phosphatase 2A (PP2A) critically regulates cell signaling and is a human tumor suppressor. PP2A complexes are modulated by proteins such as cancerous inhibitor of protein phosphatase 2A (CIP2A), protein phosphatase methylesterase 1 (PME-1), and SET nuclear proto-oncogene (SET) that often are deregulated in cancers. However, how they impact cellular phosphorylation and how redundant they are in cellular regulation is poorly understood. Here, we conducted a systematic phosphoproteomics screen for phosphotargets modulated by siRNA-mediated depletion of CIP2A, PME-1, and SET (to reactivate PP2A) or the scaffolding A-subunit of PP2A (PPP2R1A) (to inhibit PP2A) in HeLa cells. We identified PP2A-modulated targets in diverse cellular pathways, including kinase signaling, cytoskeleton, RNA splicing, DNA repair, and nuclear lamina. The results indicate nonredundancy among CIP2A, PME-1, and SET in phosphotarget regulation. Notably, PP2A inhibition or reactivation affected largely distinct phosphopeptides, introducing a concept of nonoverlapping phosphatase inhibition- and activation-responsive sites (PIRS and PARS, respectively). This phenomenon is explained by the PPP2R1A inhibition impacting primarily dephosphorylated threonines, whereas PP2A reactivation results in dephosphorylation of clustered and acidophilic sites. Using comprehensive drug-sensitivity screening in PP2A-modulated cells to evaluate the functional impact of PP2A across diverse cellular pathways targeted by these drugs, we found that consistent with global phosphoproteome effects, PP2A modulations broadly affect responses to more than 200 drugs inhibiting a broad spectrum of cancer-relevant targets. These findings advance our understanding of the phosphoproteins, pharmacological responses, and cellular processes regulated by PP2A modulation and may enable the development of combination therapies.Entities:
Keywords: AURK inhibitor; LMNA; cancer; drug screening; nucleophosmin; phosphatase activation-responsive site (PARS); phosphatase inhibition-responsive site (PIRS); phosphoproteomics; protein phosphatase 2 (PP2A); systems biology
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Year: 2020 PMID: 32071079 PMCID: PMC7105317 DOI: 10.1074/jbc.RA119.011265
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157