MEK1 mutations, but not ERK2 mutations, occur in melanomas and colon carcinomas, but none in thyroid carcinomas

被引:60
作者
Murugan, Avaniyapuram Kannan [1 ]
Dong, Jianli [2 ]
Xie, Jingwu [3 ]
Xing, Mingzhao [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Div Endocrinol & Metab, Baltimore, MD 21287 USA
[2] Univ Texas Med Branch, Dept Pathol, Galveston, TX USA
[3] Univ Texas Med Branch, Dept Pharmacol & Toxicol, Galveston, TX USA
关键词
MEK1; mutation; ERK2; thyroid cancer; colon cancer; melanomas; CANCER-CELL LINE; SIGNALING PATHWAY; KINASE; GENES; GROWTH; DOMAIN;
D O I
10.4161/cc.8.13.8710
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitogen-activated protein kinase (MAPK) signaling pathway plays an important role in the pathogenesis of melanoma, colon cancer and thyroid cancer, which commonly harbor RAS and BRAF mutations. However, mutations in exon 2 of MEK1 and exon 7 of ERK2 have not been investigated in these cancers although they are occasionally found in some other cancers or cell lines. In this study, we performed mutational analysis to search for these mutations in 185 samples, including 167 tumor samples and 18 cell lines of melanoma, colon cancer and thyroid cancer. We found one MEK1 mutation in 1 of 37 (3%) melanoma tumor samples and another MEK1 mutation in 1 of 45 (2.2%) colon cancer samples. We did not find any MEK1 mutation in 99 thyroid tumor samples and 12 thyroid cancer cell lines. We also did not find any ERK2 mutation in melanoma, colon cancer and thyroid cancer. We thus report for the first time a low prevalence of MEK1 mutations in melanoma and colon cancer. Both of the two mutants have been demonstrated to be activating in the MAPK signaling pathway and may therefore provide potential target for effective therapy in cases of melanomas and colon cancer harboring these mutations.
引用
收藏
页码:2122 / 2124
页数:3
相关论文
共 14 条
[1]  
Arvind R, 2005, INT J ONCOL, V27, P1499
[2]   Mutation analysis of the coding sequences of MEK-1 and MEK-2 genes in human lung cancer cell lines [J].
Bansal, A ;
Ramirez, RD ;
Minna, JD .
ONCOGENE, 1997, 14 (10) :1231-1234
[3]  
BOTTORFF D, 1995, MOL CELL BIOL, V15, P5113
[4]   Mutations of the BRAF gene in human cancer [J].
Davies, H ;
Bignell, GR ;
Cox, C ;
Stephens, P ;
Edkins, S ;
Clegg, S ;
Teague, J ;
Woffendin, H ;
Garnett, MJ ;
Bottomley, W ;
Davis, N ;
Dicks, N ;
Ewing, R ;
Floyd, Y ;
Gray, K ;
Hall, S ;
Hawes, R ;
Hughes, J ;
Kosmidou, V ;
Menzies, A ;
Mould, C ;
Parker, A ;
Stevens, C ;
Watt, S ;
Hooper, S ;
Wilson, R ;
Jayatilake, H ;
Gusterson, BA ;
Cooper, C ;
Shipley, J ;
Hargrave, D ;
Pritchard-Jones, K ;
Maitland, N ;
Chenevix-Trench, G ;
Riggins, GJ ;
Bigner, DD ;
Palmieri, G ;
Cossu, A ;
Flanagan, A ;
Nicholson, A ;
Ho, JWC ;
Leung, SY ;
Yuen, ST ;
Weber, BL ;
Siegler, HF ;
Darrow, TL ;
Paterson, H ;
Marais, R ;
Marshall, CJ ;
Wooster, R .
NATURE, 2002, 417 (6892) :949-954
[5]   Mutation Analysis of BRAF, MEK1 and MEK2 in 15 Ovarian Cancer Cell Lines: Implications for Therapy [J].
Estep, Anne L. ;
Palmer, Chana ;
McCormick, Frank ;
Rauen, Katherine A. .
PLOS ONE, 2007, 2 (12)
[6]   Constitutive activation of the 41-/43-kDa mitogen-activated protein kinase signaling pathway in human tumors [J].
Hoshino, R ;
Chatani, Y ;
Yamori, T ;
Tsuruo, T ;
Oka, H ;
Yoshida, O ;
Shimada, Y ;
Ari-i, S ;
Wada, H ;
Fujimoto, J ;
Kohno, M .
ONCOGENE, 1999, 18 (03) :813-822
[7]   Ras oncogenes: split personalities [J].
Karnoub, Antoine E. ;
Weinberg, Robert A. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2008, 9 (07) :517-531
[8]   ERK2 CD domain mutation from a human cancer cell line enhanced anchorage-independent cell growth and abnormality in Drosophila [J].
Mahalingam, Marthandan ;
Arvind, Ramanathan ;
Ida, Hiroyuki ;
Murugan, Avaniyapuram Kannan ;
Yamaguchi, Masamitsu ;
Tsuchida, Nobuo .
ONCOLOGY REPORTS, 2008, 20 (04) :957-962
[9]   TRANSFORMATION OF MAMMALIAN-CELLS BY CONSTITUTIVELY ACTIVE MAP KINASE KINASE [J].
MANSOUR, SJ ;
MATTEN, WT ;
HERMANN, AS ;
CANDIA, JM ;
RONG, S ;
FUKASAWA, K ;
VANDEWOUDE, GF ;
AHN, NG .
SCIENCE, 1994, 265 (5174) :966-970
[10]   Novel MEK1 mutation identified by mutational analysis of epidermal growth factor receptor signaling pathway genes in lung adenocarcinoma [J].
Marks, Jenifer L. ;
Gong, Yixuan ;
Chitale, Dhananjay ;
Golas, Ben ;
McLellan, Michael D. ;
Kasai, Yumi ;
Ding, Li ;
Mardis, Elaine R. ;
Wilson, Richard K. ;
Solit, David ;
Levine, Ross ;
Michel, Kathrin ;
Thomas, Roman K. ;
Rusch, Valerie W. ;
Ladanyi, Marc ;
Pao, William .
CANCER RESEARCH, 2008, 68 (14) :5524-5528