4.8 Article

LARG at chromosome 11q23 has functional characteristics of a tumor suppressor in human breast and colorectal cancer

Journal

ONCOGENE
Volume 28, Issue 47, Pages 4189-4200

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/onc.2009.266

Keywords

LARG; tumor suppressor; breast cancer; colorectal cancer

Funding

  1. National Medical Research Council (NMRC) of Singapore [NMRC/0076/1995, NMRC/0440/2000, NMRC/0570/2001, NMRC/0843/2004]
  2. SingHealth Foundation [SHF/FG235P/2005]
  3. Singapore Cancer Society
  4. SGH Research Fund
  5. Cancer Research Education Fund
  6. NCC and Department of Clinical Research, SGH
  7. US Department of Energy [DE-AC02-05CH11231, USAMRMC BC 061995]
  8. National Institutes of Health, National Cancer Institute [P50 CA 58207, P50 CA 83639, P30 CA 82103, U54 CA 112970, U24 CA 126477, P01 CA 64602]
  9. National Human Genome Research Institute [U24 CA 126551]
  10. SmithKline Beecham Corporation

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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 (n = 11), 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 (P = 0.00334). 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. Oncogene (2009) 28, 4189-4200; doi: 10.1038/onc.2009.266; published online 7 September 2009

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