Please use this identifier to cite or link to this item: https://doi.org/10.1038/onc.2009.266
Title: LARG at chromosome 11q23 has functional characteristics of a tumor suppressor in human breast and colorectal cancer
Authors: Ong, D.C.T.
Ho, Y.M.
Rudduck, C.
Chin, K.
Kuo, W.-L.
Lie, D.K.H.
Chua, C.L.M.
Tan, P.H.
Eu, K.W.
Seow-Choen, F.
Wong, C.Y.
Hong, G.S.
Gray, J.W.
Lee, A.S.G. 
Keywords: Breast cancer
Colorectal cancer
LARG
Tumor suppressor
Issue Date: Nov-2009
Citation: Ong, D.C.T., Ho, Y.M., Rudduck, C., Chin, K., Kuo, W.-L., Lie, D.K.H., Chua, C.L.M., Tan, P.H., Eu, K.W., Seow-Choen, F., Wong, C.Y., Hong, G.S., Gray, J.W., Lee, A.S.G. (2009-11). LARG at chromosome 11q23 has functional characteristics of a tumor suppressor in human breast and colorectal cancer. Oncogene 28 (47) : 4189-4200. ScholarBank@NUS Repository. https://doi.org/10.1038/onc.2009.266
Abstract: Deletion of 11q23-q24 is frequent in a diverse variety of malignancies, including breast and colorectal carcinoma, implicating the presence of a tumor suppressor gene at that chromosomal region. We examined a 6-Mb region on 11q23 by high-resolution deletion mapping, using both loss of heterozygosity analysis and customized microarray comparative genomic hybridization. LARG (leukemia-associated Rho guanine-nucleotide exchange factor) (also called ARHGEF12), identified from the analysed region, is frequently underexpressed in breast and colorectal carcinomas with a reduced expression observed in all breast cancer cell lines (n11), in 12 of 38 (32%) primary breast cancers, 5 of 10 (50%) colorectal cell lines and in 20 of 37 (54%) primary colorectal cancers. Underexpression of the LARG transcript was significantly associated with genomic loss (P0.00334). Hypermethylation of the LARG promoter was not detected in either breast or colorectal cancer, and treatment of four breast and four colorectal cancer cell lines with 5-aza-2′-deoxycytidine and/or trichostatin A did not result in a reactivation of LARG. Enforced expression of LARG in breast and colorectal cancer cells by stable transfection resulted in reduced cell proliferation and colony formation, as well as in a markedly slower cell migration rate in colorectal cancer cells, providing functional evidence for LARG as a candidate tumor suppressor gene. © 2009 Macmillan Publishers Limited All rights reserved.
Source Title: Oncogene
URI: http://scholarbank.nus.edu.sg/handle/10635/120838
ISSN: 09509232
DOI: 10.1038/onc.2009.266
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