Although kinase oncogenes are well-characterized drivers of cancer development, much less is known regarding the role of phosphatases in transformation. The serine-threonine protein phosphatase 2A (PP2A) is implicated in the regulation of numerous signaling pathways and may function as a tumor suppressor. PP2A is a heterotrimeric protein complex, and several isoforms exist for each of the three subunits, creating a diverse family of related enzymes that regulate specific physiological functions. The diversity of PP2A heterotrimers has complicated previous efforts to establish the cellular function of specific PP2A subunits. I propose to take a three-tiered approach toward a systematic characterization of PP2A complexes in cancer progression. Using loss of function experiments I plan to assess the contribution of particular PP2A complexes in human cell transformation. By using genome scale approaches, I will determine alterations of particular PP2A regulatory subunits in human cancers. I will then focus on deciphering the molecular roles of specific PP2A complexes in tumor suppression through a directed proteomics approach together with cell transformation assays. ? ? Public Health Relevance: These studies represent primary steps toward the identification of new targets that may have diagnostic and therapeutic potential in the treatment of cancer. ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Career Transition Award (K99)
Project #
1K99CA125974-01A2
Application #
7471708
Study Section
Subcommittee G - Education (NCI)
Program Officer
Lohrey, Nancy
Project Start
2008-06-01
Project End
2009-05-31
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
1
Fiscal Year
2008
Total Cost
$102,952
Indirect Cost
Name
Dana-Farber Cancer Institute
Department
Type
DUNS #
076580745
City
Boston
State
MA
Country
United States
Zip Code
02215
Sablina, Anna A; Hector, Melissa; Colpaert, Nathalie et al. (2010) Identification of PP2A complexes and pathways involved in cell transformation. Cancer Res 70:10474-84