TY - JOUR
T1 - KIAA1199 interacts with glycogen phosphorylase kinase ß-subunit (PHKB) to promote glycogen breakdown and cancer cell survival
AU - Terashima, Masato
AU - Fujita, Yoshihiko
AU - Togashi, Yosuke
AU - Sakai, Kazuko
AU - De Velasco, Marco A.
AU - Tomida, Shuta
AU - Nishio, Kazuto
PY - 2014
Y1 - 2014
N2 - The KIAA1199 gene was first discovered to be associated with non-syndromic hearing loss. Recently, several reports have shown that the up-regulation of KIAA1199 is associated with cancer cell migration or invasion and a poor prognosis. These findings indicate that KIAA1199 may be a novel target for cancer therapy. Therefore, we explored in detail the function of KIAA1199 in cancer cells. In this study, we investigated the interaction of KIAA1199 protein with intracellular proteins in cancer cells. To this end, we expressed KIAA1199-MBP fusion protein and performed a pull-down assay. In addition, KIAA1199-overexpressing cancer cell lines were constructed using a retroviral vector and were used for further experiments. A pull-down analysis showed that the glycogen phosphorylase kinase ß-subunit (PHKB) interacted with the C-terminal region of KIAA1199 protein. Furthermore, we observed the interaction of KIAA1199 with glycogen phosphorylase brain form (PYGB) under serum-free conditions. The interaction promoted glycogen breakdown and cancer cell survival. Our findings indicate that KIAA1199 plays an important role in glycogen breakdown and cancer cell survival and that it may represent a novel target for cancer therapy.
AB - The KIAA1199 gene was first discovered to be associated with non-syndromic hearing loss. Recently, several reports have shown that the up-regulation of KIAA1199 is associated with cancer cell migration or invasion and a poor prognosis. These findings indicate that KIAA1199 may be a novel target for cancer therapy. Therefore, we explored in detail the function of KIAA1199 in cancer cells. In this study, we investigated the interaction of KIAA1199 protein with intracellular proteins in cancer cells. To this end, we expressed KIAA1199-MBP fusion protein and performed a pull-down assay. In addition, KIAA1199-overexpressing cancer cell lines were constructed using a retroviral vector and were used for further experiments. A pull-down analysis showed that the glycogen phosphorylase kinase ß-subunit (PHKB) interacted with the C-terminal region of KIAA1199 protein. Furthermore, we observed the interaction of KIAA1199 with glycogen phosphorylase brain form (PYGB) under serum-free conditions. The interaction promoted glycogen breakdown and cancer cell survival. Our findings indicate that KIAA1199 plays an important role in glycogen breakdown and cancer cell survival and that it may represent a novel target for cancer therapy.
KW - Glycogen breakdown
KW - Glycogen phosphorylase brain form
KW - Glycogen phosphorylase kinase ß-subunit
KW - KIAA1199
UR - http://www.scopus.com/inward/record.url?scp=84907081373&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84907081373&partnerID=8YFLogxK
U2 - 10.18632/oncotarget.2220
DO - 10.18632/oncotarget.2220
M3 - Article
C2 - 25051373
AN - SCOPUS:84907081373
SN - 1949-2553
VL - 5
SP - 7040
EP - 7050
JO - Oncotarget
JF - Oncotarget
IS - 16
ER -