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  4. Radiation-induced VEGF-C expression and endothelial cell proliferation in lung cancer [Strahleninduzierte VEGF-C-Expression und endotheliale Zellteilung bei Lungenkrebs]
 
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Radiation-induced VEGF-C expression and endothelial cell proliferation in lung cancer [Strahleninduzierte VEGF-C-Expression und endotheliale Zellteilung bei Lungenkrebs]

Journal
Strahlentherapie und Onkologie
Journal Volume
190
Journal Issue
12
Pages
1154-1162
Date Issued
2014
Author(s)
YU-HSUAN CHEN  
Pan S.-L.
Wang J.-C.
SUNG-HSIN KUO  
CHIA-HSIEN CHENG  
Teng C.-M.
DOI
10.1007/s00066-014-0708-z
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84911808155&doi=10.1007%2fs00066-014-0708-z&partnerID=40&md5=5fa6c0ede586c7671f9564a4b60e0ba1
https://scholars.lib.ntu.edu.tw/handle/123456789/623286
Abstract
BACKGROUND: The present study was undertaken to investigate whether radiation induces the expression of vascular endothelial growth factor C (VEGF-C) through activation of the PI3K/Akt/mTOR pathway,subsequently affecting endothelial cells. MATERIALS AND METHODS: Radiotherapy-induced tumor micro-lymphatic vessel density (MLVD) was determined in a lung cancer xenograft model established in SCID mice. The protein expression and phosphorylation of members of the PI3K/Akt/mTOR pathway and VEGF-C secretion and mRNA expression in irradiated lung cancer cells were assessed by Western blot analysis, enzyme-linked immunosorbent assays (ELISAs), and reverse transcriptase-polymerase chain reaction (RT-PCR). Moreover, specific chemical inhibitors were used to evaluate the role of the PI3K/Akt/mTOR signaling pathway. Conditioned medium (CM) from irradiated control-siRNA or VEGF-C-siRNA-expressing A549 cells was used to evaluate the proliferation of endothelial cells by the MTT assay. RESULTS: Radiation increased VEGF-C expression in a dose-dependent manner over time at the protein but not at the mRNA level. Radiation also up-regulated the phosphorylation of Akt, mTOR, 4EBP, and eIF4E, but not of p70S6K. Radiation-induced VEGF-C expression was down-regulated by LY294002 and rapamycin (both p < 0.05). Furthermore, CM from irradiated A549 cells enhanced human umbilical vein endothelial cell (HUVEC) and lymphatic endothelial cell (LEC) proliferation, which was not observed with CM from irradiated VEGF-C-siRNA-expressing A549 cells. CONCLUSIONS: Radiation-induced activation of the PI3K/Akt/mTOR signaling pathway increases VEGF-C expression in lung cancer cells, thereby promoting endothelial cell proliferation.
SDGs

[SDGs]SDG3

Publisher
Urban und Vogel GmbH
Type
journal article

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