Protein phosphatase 2A: a target for anticancer therapy

D Perrotti, P Neviani - The lancet oncology, 2013 - thelancet.com
Summary Protein phosphatase 2A (PP2A), one of the main serine–threonine phosphatases
in mammalian cells, maintains cell homoeostasis by counteracting most of the kinase-driven …

Sphingolipids: regulators of crosstalk between apoptosis and autophagy

MM Young, M Kester, HG Wang - Journal of lipid research, 2013 - ASBMB
Apoptosis and autophagy are two evolutionarily conserved processes that maintain
homeostasis during stress. Although the two pathways utilize fundamentally distinct …

Sphingosine analogue drug FTY720 targets I2PP2A/SET and mediates lung tumour suppression via activation of PP2A‐RIPK1‐dependent necroptosis

SA Saddoughi, S Gencer, YK Peterson… - EMBO molecular …, 2013 - embopress.org
Mechanisms that alter protein phosphatase 2A (PP2A)‐dependent lung tumour suppression
via the I2PP2A/SET oncoprotein are unknown. We show here that the tumour suppressor …

The key role of sphingolipid metabolism in cancer: New therapeutic targets, diagnostic and prognostic values, and anti-tumor immunotherapy resistance

RZ Li, XR Wang, J Wang, C **e, XX Wang… - Frontiers in …, 2022 - frontiersin.org
Biologically active sphingolipids are closely related to the growth, differentiation, aging, and
apoptosis of cancer cells. Some sphingolipids, such as ceramides, are favorable metabolites …

FTY720 induces ferroptosis and autophagy via PP2A/AMPK pathway in multiple myeloma cells

Y Zhong, F Tian, H Ma, H Wang, W Yang, Z Liu, A Liao - Life sciences, 2020 - Elsevier
Aims Multiple myeloma (MM) is the second hematological plasma cell malignany and
sensitive to fingolimod (FTY720), a novel immunosuppressant. Previous study shows …

[HTML][HTML] Protein phosphatase 2A as a therapeutic target in inflammation and neurodegeneration

AR Clark, M Ohlmeyer - Pharmacology & therapeutics, 2019 - Elsevier
Abstract Protein phosphatase 2A (PP2A) is a highly complex heterotrimeric enzyme that
catalyzes the selective removal of phosphate groups from protein serine and threonine …

Inhibition of cathepsin S induces autophagy and apoptosis in human glioblastoma cell lines through ROS-mediated PI3K/AKT/mTOR/p70S6K and JNK signaling …

L Zhang, H Wang, J Xu, J Zhu, K Ding - Toxicology letters, 2014 - Elsevier
Cathepsin S is a lysosomal cysteine protease that is overexpressed in various cancer
models and plays important role in tumorigenesis, however the mechanisms are unclear. In …

Molecular pharmacology and novel potential therapeutic applications of fingolimod

S Pournajaf, L Dargahi, M Javan… - Frontiers in …, 2022 - frontiersin.org
Fingolimod is a well-tolerated, highly effective disease-modifying therapy successfully
utilized in the management of multiple sclerosis. The active metabolite, fingolimod …

HMGB1-mediated autophagy promotes docetaxel resistance in human lung adenocarcinoma

B Pan, D Chen, J Huang, R Wang, B Feng, H Song… - Molecular cancer, 2014 - Springer
Background Docetaxel resistance remains a major obstacle in the treatment of non-small
cell lung cancer (NSCLC). High-mobility group box 1 (HMGB1) has been shown to promote …

[HTML][HTML] Ceramide species are elevated in human breast cancer and are associated with less aggressiveness

K Moro, T Kawaguchi, J Tsuchida, E Gabriel, Q Qi… - Oncotarget, 2018 - ncbi.nlm.nih.gov
Sphingolipids have emerged as key regulatory molecules in cancer cell survival and death.
Although important roles of sphingolipids in breast cancer progression have been reported …