Glypican-3 reexpression regulates apoptosis in murine adenocarcinoma mammary cells modulating PI3K/Akt and p38MAPK signaling pathways


Autoria(s): BUCHANAN, C.; STIGLIANO, I.; GARAY-MALPARTIDA, H. M.; GOMES, L. Rodrigues; PURICELLI, L.; SOGAYAR, M. C.; JOFFE, E. Bal de Kier; PETERS, M. G.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/10/2012

18/10/2012

2010

Resumo

Glypican-3 (GPC3) is a proteoglycan involved in proliferation and cell survival. Several reports demonstrated that GPC3 is downregulated in some tumors, such as breast cancer. Previously, we determined that GPC3 reexpression in the murine mammary adenocarcinoma LM3 cells induced an impairment of their invasive and metastatic capacities, associated with a decrease of their motility and an increase of their cell death. We demonstrated that GPC3 inhibits canonical Wnt signaling, as well as it activates non canonical pathway. Now, we identified signaling pathways responsible for the pro-apoptotic role of GPC3 in LM3 cells. We found for the first time that GPC3 inhibits the PI3K/Akt anti-apoptotic pathway while it stimulates the p38MAPK stress-activated one. We report a concomitant modulation of CDK inhibitors as well as of pro- and anti-apoptotic molecules. Our results provide new clues regarding the mechanism involved in the modulation induced by GPC3 of mammary tumor cell growth and survival.

FONCyT[PICT 14088]

FONCyT[BID 1728/OC-AR]

FONCyT[PICT 00220]

University of Buenos Aires[UBACyT M068], Argentina

Identificador

BREAST CANCER RESEARCH AND TREATMENT, v.119, n.3, p.559-574, 2010

0167-6806

http://producao.usp.br/handle/BDPI/17144

10.1007/s10549-009-0362-9

http://dx.doi.org/10.1007/s10549-009-0362-9

Idioma(s)

eng

Publicador

SPRINGER

Relação

Breast Cancer Research and Treatment

Direitos

restrictedAccess

Copyright SPRINGER

Palavras-Chave #Glypican-3 #Apoptosis #PI3K/Akt pathway #p38MAPK pathway #Breast cancer #GOLABI-BEHMEL-SYNDROME #HEPARAN-SULFATE PROTEOGLYCANS #BREAST-CANCER #OVERGROWTH SYNDROME #GENE #EXPRESSION #PROTEIN #MODEL #GPC3 #P53 #Oncology
Tipo

article

original article

publishedVersion