TY - JOUR
T1 - PTEN function
T2 - The long and the short of it
AU - Hopkins, Benjamin D.
AU - Hodakoski, Cindy
AU - Barrows, Douglas
AU - Mense, Sarah M.
AU - Parsons, Ramon E.
PY - 2014/4
Y1 - 2014/4
N2 - Phosphatase and tensin homolog deleted on chromosome ten (PTEN) is a phosphatase that is frequently altered in cancer. PTEN has phosphatase-dependent and -independent roles, and genetic alterations in PTEN lead to deregulation of protein synthesis, the cell cycle, migration, growth, DNA repair, and survival signaling. PTEN localization, stability, conformation, and phosphatase activity are controlled by an array of protein-protein interactions and post-translational modifications. Thus, PTEN-interacting and -modifying proteins have profound effects on the tumor suppressive functions of PTEN. Moreover, recent studies identified mechanisms by which PTEN can exit cells, via either exosomal export or secretion, and act on neighboring cells. This review focuses on modes of PTEN protein regulation and ways in which perturbations in this regulation may lead to disease.
AB - Phosphatase and tensin homolog deleted on chromosome ten (PTEN) is a phosphatase that is frequently altered in cancer. PTEN has phosphatase-dependent and -independent roles, and genetic alterations in PTEN lead to deregulation of protein synthesis, the cell cycle, migration, growth, DNA repair, and survival signaling. PTEN localization, stability, conformation, and phosphatase activity are controlled by an array of protein-protein interactions and post-translational modifications. Thus, PTEN-interacting and -modifying proteins have profound effects on the tumor suppressive functions of PTEN. Moreover, recent studies identified mechanisms by which PTEN can exit cells, via either exosomal export or secretion, and act on neighboring cells. This review focuses on modes of PTEN protein regulation and ways in which perturbations in this regulation may lead to disease.
KW - PI3K signaling
KW - PTEN
KW - PTEN-Long
UR - http://www.scopus.com/inward/record.url?scp=84897391926&partnerID=8YFLogxK
U2 - 10.1016/j.tibs.2014.02.006
DO - 10.1016/j.tibs.2014.02.006
M3 - Review article
C2 - 24656806
AN - SCOPUS:84897391926
SN - 0968-0004
VL - 39
SP - 183
EP - 190
JO - Trends in Biochemical Sciences
JF - Trends in Biochemical Sciences
IS - 4
ER -