The tumor suppressor phosphatase PP2A-B56α regulates stemness and promotes the initiation of malignancies in a novel murine model

Mahnaz Janghorban, Ellen M. Langer, Xiaoyan Wang, Derek Zachman, Colin J. Daniel, Jody Hooper, William Fleming, Anupriya Agarwal, Rosalie Sears

Research output: Contribution to journalArticle

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Abstract

Protein phosphatase 2A (PP2A) is a ubiquitously expressed Serine-Threonine phosphatase mediating 30–50% of protein phosphatase activity. PP2A functions as a heterotrimeric complex, with the B subunits directing target specificity to regulate the activity of many key pathways that control cellular phenotypes. PP2A-B56α has been shown to play a tumor suppressor role and to negatively control c-MYC stability and activity. Loss of B56α promotes cellular transformation, likely at least in part through its regulation of c-MYC. Here we report generation of a B56α hypomorph mouse with very low B56α expression that we used to study the physiologic activity of the PP2A-B56α phosphatase. The predominant phenotype we observed in mice with B56α deficiency in the whole body was spontaneous skin lesion formation with hyperproliferation of the epidermis, hair follicles and sebaceous glands. Increased levels of c-MYC phosphorylation on Serine62 and c-MYC activity were observed in the skin lesions of the B56αhm/hm mice. B56α deficiency was found to increase the number of skin stem cells, and consistent with this, papilloma initiation was accelerated in a carcinogenesis model. Further analysis of additional tissues revealed increased inflammation in spleen, liver, lung, and intestinal lymph nodes as well as in the skin lesions, resembling elevated extramedullary hematopoiesis phenotypes in the B56αhm/hm mice. We also observed an increase in the clonogenicity of bone marrow stem cells in B56αhm/hm mice. Overall, this model suggests that B56α is important for stem cells to maintain homeostasis and that B56α loss leading to increased activity of important oncogenes, including c-MYC, can result in aberrant cell growth and increased stem cells that can contribute to the initiation of malignancy.

Original languageEnglish (US)
Article numbere0188910
JournalPLoS One
Volume12
Issue number11
DOIs
StatePublished - Nov 1 2017

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Tumor Suppressor Proteins
Protein Phosphatase 2
phosphoprotein phosphatase
Phosphatases
Stem cells
Phosphoric Monoester Hydrolases
Tumors
Skin
animal models
stem cells
skin lesions
Stem Cells
neoplasms
Phosphoprotein Phosphatases
mice
Neoplasms
Phenotype
phenotype
Phosphorylation
Extramedullary Hematopoiesis

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)

Cite this

The tumor suppressor phosphatase PP2A-B56α regulates stemness and promotes the initiation of malignancies in a novel murine model. / Janghorban, Mahnaz; Langer, Ellen M.; Wang, Xiaoyan; Zachman, Derek; Daniel, Colin J.; Hooper, Jody; Fleming, William; Agarwal, Anupriya; Sears, Rosalie.

In: PLoS One, Vol. 12, No. 11, e0188910, 01.11.2017.

Research output: Contribution to journalArticle

Janghorban, Mahnaz ; Langer, Ellen M. ; Wang, Xiaoyan ; Zachman, Derek ; Daniel, Colin J. ; Hooper, Jody ; Fleming, William ; Agarwal, Anupriya ; Sears, Rosalie. / The tumor suppressor phosphatase PP2A-B56α regulates stemness and promotes the initiation of malignancies in a novel murine model. In: PLoS One. 2017 ; Vol. 12, No. 11.
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