Leukemia inhibitory factor can mediate Ras/Raf/MEK/ERK-induced growth inhibitory signaling in medullary thyroid cancer cells

被引:61
作者
Arthan, Dumrongkiet [1 ]
Hong, Seung-Keun [1 ]
Park, Jong-In [1 ]
机构
[1] Med Coll Wisconsin, Dept Biochem, Milwaukee, WI 53226 USA
关键词
Medullary thyroid cancer; Leukemia inhibitory factor; Ras/Raf; Ret; Growth inhibition; ONCOGENE-INDUCED SENESCENCE; FACTOR/JAK/STAT PATHWAY; RET PROTOONCOGENE; DIFFERENTIATION; KINASE; ACTIVATION; ARREST; TRANSFORMATION; EXPRESSION; PHENOTYPE;
D O I
10.1016/j.canlet.2010.04.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Medullary thyroid carcinoma (MTC) is a multiple endocrine neoplasia type 2 syndrome caused by mutations in extracellular receptor or intracellular kinase domains of the RET proto-oncogene. Activation of the Ras/Raf/MEK/ERK pathway can lead to growth arrest by secreting leukemia inhibitory factor (LIF) in MTC cells harboring a RET receptor domain mutation. Here, we report that Ras/Raf/MEK/ERK can also mediate, via LIF, growth inhibition in MTC cells harboring a RET kinase domain mutation. Ras/Raf/MEK/ERK activation was sufficient to induce growth inhibition and LIF expression in the human MTC line MZ-CRC-1. Presence of LIF-mediated signaling was determined by blocking the activity of culture medium conditioned by Raf-activated cells using anti-LIF neutralizing antibody. In addition, recombinant LIF effectively suppressed cell proliferation via cell cycle arrest in G0/G1 phase. Expression of dominant negative STAT3 abrogated LIF effects, indicating that LIF mediates its signaling through the JAK/STAT3 pathway. These results suggest that growth inhibition and activation of the autocrine/paracrine signaling through LIF/JAK/STAT may be a common response to Ras/Raf activation in different MTC types, and justify further evaluation of LIF as a potential anticancer agent for MTC. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:31 / 41
页数:11
相关论文
共 51 条
[1]
Chemokine signaling via the CXCR2 receptor reinforces senescence [J].
Acosta, Juan C. ;
O'Loghlen, Ana ;
Banito, Ana ;
Guijarro, Maria V. ;
Augert, Arnaud ;
Raguz, Selina ;
Fumagalli, Marzia ;
Da Costa, Marco ;
Brown, Celia ;
Popov, Nikolay ;
Takatsu, Yoshihiro ;
Melamed, Jonathan ;
di Fagagna, Fabrizio d'Adda ;
Bernard, David ;
Hernando, Eva ;
Gil, Jesus .
CELL, 2008, 133 (06) :1006-1018
[2]
Leukemia-inhibitory factor - Neuroimmune modulator of endocrine function [J].
Auernhammer, CJ ;
Melmed, S .
ENDOCRINE REVIEWS, 2000, 21 (03) :313-345
[3]
Oncogene-induced senescence: Putting the brakes on tumor development [J].
Braig, M ;
Schmitt, CA .
CANCER RESEARCH, 2006, 66 (06) :2881-2884
[4]
Stat3 as an oncogene [J].
Bromberg, JF ;
Wrzeszczynska, MH ;
Devgan, G ;
Zhao, YX ;
Pestell, RG ;
Albanese, C ;
Darnell, JE .
CELL, 1999, 98 (03) :295-303
[5]
Stat3 activation is required for cellular transformation by v-src [J].
Bromberg, JF ;
Horvath, CM ;
Besser, D ;
Lathem, WW ;
Darnell, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (05) :2553-2558
[6]
ERK and cell death: Mechanisms of ERK-induced cell death - apoptosis, autophagy and senescence [J].
Cagnol, Sebastien ;
Chambard, Jean-Claude .
FEBS JOURNAL, 2010, 277 (01) :2-21
[7]
CARSON EB, 1995, CANCER RES, V55, P2048
[8]
Post-transcriptional silencing of RET occurs, but is not required, during raf-1 mediated differentiation of medullary thyroid carcinoma cells [J].
Carson-Walter, EB ;
Smith, DP ;
Ponder, BAJ ;
Baylin, SB ;
Nelkin, BD .
ONCOGENE, 1998, 17 (03) :367-376
[9]
Interferon-inducible IFI16 protein in human cancers and autoimmune diseases [J].
Choubey, Divaker ;
Deka, Ranjan ;
Ho, Shuk-mei .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2008, 13 :598-608
[10]
A randomized, double-blinded, placebo-controlled phase II trial of recombinant human leukemia inhibitory factor (rhuLIF, emfilermin, AN1424) to prevent chemotherapy induced peripheral neuropathy [J].
Davis, ID ;
Kiers, L ;
MacGregor, L ;
Quinn, M ;
Arezzo, J ;
Green, M ;
Rosenthal, M ;
Chia, M ;
Michael, M ;
Bartley, P ;
Harrison, L ;
Daly, M .
CLINICAL CANCER RESEARCH, 2005, 11 (05) :1890-1898