| Literature DB >> 25385028 |
Tiansuo Zhao1, He Ren1, Jing Li1, Jing Chen1, Huan Zhang1, Wen Xin1, Yan Sun1, Lei Sun1, Yongwei Yang1, Junwei Sun1, Xiuchao Wang1, Song Gao1, Chongbiao Huang1, Huafeng Zhang2, Shengyu Yang3, Jihui Hao4.
Abstract
LASP1 is an actin-binding protein associated with actin assembly dynamics in cancer cells. Here, we report that LASP1 is overexpressed in pancreatic ductal adenocarcinoma (PDAC) where it promotes invasion and metastasis. We found that LASP1 overexpression in PDAC cells was mediated by HIF1α through direct binding to a hypoxia response element in the LASP1 promoter. HIF1α stimulated LASP1 expression in PDAC cells in vitro and mouse tumor xenografts in vivo. Clinically, LASP1 overexpression in PDAC patient specimens was associated significantly with lymph node metastasis and overall survival. Overall, our results defined LASP1 as a direct target gene for HIF1α upregulation that is critical for metastatic progression of PDAC. ©2014 American Association for Cancer Research.Entities:
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Year: 2014 PMID: 25385028 PMCID: PMC4286473 DOI: 10.1158/0008-5472.CAN-14-2040
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701