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KERD
논문KCI 등재

대장 샘종과 샘암종에서 RUNX3 메칠화의 양상

RUNX3 Methylation Status in Colonic Carcinoma and Adenoma

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초록

Abstract

Background : RUNX3 is expressed throughout the luminal gastrointestinal tract. RUNX3 is on chromosome 1p36, a location considered to carry an important tumor suppressor for many types of cancers. Epigenetic silencing of RUNX3 is causally related to human gastric cancer. Methods : Colorectal cancers, adenoma, and the corresponding normal mucosa were obtained from 26 individual patients. To identify methylation of RUNX3 in colonic carcinogenesis, methylation- specific PCR was performed. Results : RUNX3 methylation was found in one case of colonic carcinoma. The normal mucosa and tubular adenoma of this case had no methylation. No other cases were found to have methylations. Conclusions : These results are very different from the findings of gastric carcinomas, where frequent DNA methylation in the vicinity of the RUNX3 promoter is found. Although, the possibility of a role of RUNX3 methylation in the colon can not be completely ruled out, these results suggest that methylation of the RUNX3 promoter region might not contribute to the adenoma-carcinoma sequence of the colon.

참고문헌 (21)

  1. "Estimates of the worldwide incidenceof 25 major cancers in 1990", 80, pp.827~841 (1999)
  2. "Mutagenic and epigenetic effects of DNAmethylation", 386, pp.107~118 (1997)
  3. "Causal relationship between the lossof RUNX3 expression and gastric cancer", 109, pp.113~124 (2002)
  4. "Report of the second internationalworkshop on human chromosome 1 mapping 1995", 72, pp.114~144 (1996)
  5. "Single-tube protocolfor the extraction of DNA or RNA from paraffin-embedded tissuesusing a starch-based adhesive", 20, pp.846~850 (1996)
  6. "Methylation-specific PCR:a novel PCR assay for methylation status of CpGislands", 93, pp.9821~9826 (1996)
  7. "the human members of the runt domaingene-family: cDNA structure, expression, and chromosomal localization", 23, pp.425~432 (1994)
  8. "Cloning, mapping and expressionof PEBP2 alpha C, a third gene encoding the mammalian Runtdomain.", 159, pp.245~248 (1995)
  9. "Mapping of the mousehomolog of the human runt domain gene,AML2, to the distal regionof mouse chromosome 4", 25, pp.603~605 (1995)
  10. "the target of multiple chromosomal translocations in humanleukemia is essential for normal fetal liver hematopoiesis", 84, pp.321~330 (1996)
  11. "Targeted disruption of Cbfa1results in a complete lack of bone formation owing to maturationalarrest of osteoblasts", 89, pp.755~764 (1997)
  12. "Cbfa1, a candidate gene forcleidocranial dysplasia syndrome,is essential for osteoblast differentiationand bone development", 89, pp.765~771 (1997)
  13. "Functions of mammalian Smad genesas revealed by targeted gene disruption in mice", 11, pp.49~58 (2000)
  14. "RUNX transcription factors as key targets ofTGF- ? superfamily signaling", 13, pp.43~47
  15. "Mutational inactivationof transforming growth factor beta receptor type II in microsatellitestable colon cancers", 59, pp.320~324 (1999)
  16. "Mad-related genesin the human", 13, pp.347~349 (1996)
  17. "Inactivation of the type II TGFbetareceptor in colon cancer cells with microsatellite instability", 268, pp.1336~1338 (1995)
  18. "Microsatellite instability and mutationsof the transforming growth factor beta type II receptor gene incolorectal cancer", 55, pp.5548~5550 (1995)
  19. "Evaluation of candidatetumour suppressor genes on chromosome 18 in colorectal cancers", 13, pp.343~346 (1996)
  20. "MADR2 maps to 18q21 andencodes a TGFbeta-regulated MAD-related protein that is functionallymutated in colorectal carcinoma", 86, pp.543~552 (1996)
  21. "5′CpG island methylation is associatedwith transcriptional silencing of the tumour suppressor p16", CDKN2, MTS1 in human cancers, natmed1995;1natmed1995;1

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