Lapatinib Inhibits Amphiregulin-induced BeWo Choriocarcinoma Cell Proliferation by Reducing ERK1/2 and AKT Signaling Pathways.

Abstract:

BACKGROUND:Human choriocarcinoma is the most aggressive type of gestational trophoblastic neoplasia. The expression of epidermal growth factor receptor (EGFR) in choriocarcinomas is significantly higher than those of trophoblastic cells in healthy placentas. Lapatinib is a potent EGFR and human epidermal growth factor receptor 2 (HER2) inhibitor that inhibits cell proliferation and induces apoptosis in various human cancer cells. Amphiregulin (AREG) is the most abundant EGFR ligand in amniotic fluid during human pregnancy. AIM:To explore the role of AREG in human choriocarcinoma cell proliferation. MATERIALS AND METHODS:The effect of lapatinib and AREG on cell proliferation was examined by the MTT assay. Western blots were used to investigate EGFR and HER2 expression, and the activation of caspase-3, extracellular signal-regulated kinases 1/2 (ERK1/2) and phosphatidylinositol 3-kinase /protein kinase B (PI3K/AKT) signaling pathways. RESULTS:Treatment with lapatinib reduced BeWo cell proliferation by inducing apoptosis. Moreover, AREG treatment stimulated BeWo cell proliferation by activating ERK1/2 and PI3K/AKT signaling pathways, which was blocked by lapatinib. CONCLUSION:Targeting EGFR/HER2 might be a useful therapeutic strategy for human choriocarcinoma.

journal_name

Anticancer Res

journal_title

Anticancer research

authors

Pires LV,Yi Y,Cheng JC,Pizzolato LS,Cordero E,Leung PCK,Brum IS

doi

10.21873/anticanres.13355

subject

Has Abstract

pub_date

2019-05-01 00:00:00

pages

2377-2383

issue

5

eissn

0250-7005

issn

1791-7530

pii

39/5/2377

journal_volume

39

pub_type

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