본문 바로가기
KERD
논문KCI 등재

대장암에서 7, 20번 염색체의 Amplification

Amplification on 7th and 20th Chromosome from Colorectal Carcinoma

2

조회

0

다운로드

0

인용

0

참고문헌

키워드

주제분류기타자연과학

초록

.

Abstract

Colorectal carcinoma from various cancers is fourth ranked occurred to Korean. Due to western dietary life, this cancer has been increased continuously. Therefore, the further study will be needed to find a candidate gene involved in the development and progression of colorectal carcinoma as well as to diagnose and treatment helpfully. The purpose of this study was designed to find a carcinogenesis gene using microsatellite marker on chromosomes 7th and 20th from 30 colon cancer patients. The amplification was investigated in order of D20S97 57% (17/30), D20S101 57% (17/30), D20S119 53% (16/30), D7S483 50% (15/30), D7S495 47% (14/30), D7S498 47% (14/30). The genetic mutation pattern depends on loci of colorectal carcinoma was shown highly amplified with 3.77 from colon cancer than with 2.08 from right colorectal carcinoma (P<0.018). The genetic mutation with lymph nodes was investigated higher with 4.13 at metastasized group than with 1.93 at non-metastasized group (P<0.001). There was no difference at comparison between histological classfication and serological CEA increase as well as on genetic mutated pattern depends on disease stage. It is suggested that the amplification on chromosomes 7q and 20q determines a pivotal role from first stage to metastasis cancer and also functions as an useful marker on diagnosis and treatment of colorectal carcinoma patients as well as follow-up checkup. Recently, the diagnosis and study using genetic analyzer are necessary for efficient application. Fortunately, several university hospitals run this genetic analyzer currently so it is expected that this method makes full use of clinical application.

참고문헌 (23)

  1. Bardi G, "Karyotyping characterization of colorectal adenocarcinomas", Genes Chromosom Cancer, 12, pp.97~109 (1995)
  2. De Angelis PM, "Chromosomal gains and losses in primary colorectal carcinomas detected by CGH and their associations with tumour DNA ploidy, genotypes and phenotypes", Br J Cancer, 80, pp.526~535 (1999)
  3. Forslund A, "Mutation and allelic loss of p53 in primary tumor DNA from potentially cured patients with colorectal carcinoma", J Clin Oncol, 19, pp.2829~2836 (2001)
  4. Garcia E, "Loss of heterozygosity in the region including the BRCA1 gene on 17q colon cancer", Cancer Genet Cytogenet, 104, pp.119~123 (1998)
  5. Irby RB, "Activating SRC mutation in a subset of advanced human colon cancers", Nat Genet, 21, pp.187~190 (1999)
  6. Kallioniemi A, "Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors", Science, 258, pp.818~821 (1992)
  7. Kambara T, "High frequency of low-level microsatellite instability in early colorectal cancer", Cancer Res, 61, pp.7743~7746 (2001)
  8. Mahlamaki EH, "Comparative genomic hybridization reveals frequent gains of 20q, 8q, 11q, 12p and 17q and losses of 18q, 9p, and 15q in pancreatic cancer", Genes Chromosom Cancer, 20, pp.383~391 (1997)
  9. Marcelo L, "Comparative genomic hybridization reveals differences in DNA copy number changes between sporadic gastric carcinomas and gastric carcinomas from patients with hereditary nonpolyposis cololectal cancer", Cancer Genet Cytogenet, 106, pp.62~65 (1998)
  10. Meijer GA, "Progression from colorectal adenoma to carcinoma is associated with non-random chromosomal gains as detected by comparative genomic hybridization", J Clin Pathol, 1, pp.901~909 (1998)
  11. Nakao K, "Genetic changes in primary colorectal cancer by comparative genomic hybridization", Surg Today, 28, pp.567~569 (1998)
  12. Nakao K, "Genetic changes in colorectal carcinoma tumors with liver metastases analyzed by comparative genomic hybridization and DNA ploidy", Cancer, 15, pp.721~726 (2001)
  13. Paredes-Zaglul A, "Analysis of colorectal cancer by comparative genomic hybridization : Evidence for induction of the metastatic phenotype by loss of tumor suppressor genes", Clin Cancer Res, 4, pp.879~886 (1998)
  14. Ried T, "Comparative genomic hybridization reveals a specific pattern of chromosomal gains and losses during the genesis of colorectal tumors", Genes Chromosom Cancer, 15, pp.234~245 (1996)
  15. Rolf I, "Evaluation of heterozygosity", allelic imbalance scoring in tumor DNA, 2001, pp.127, 64~70
  16. Savelieva E, "20q gain associates with immortalization: 20q13.2 amplification correlates with genome instability in human papillomavirus 16 E7 transformed human uroepitherial cells", Oncogene, 14, pp.551~560 (1997)
  17. Tina B, "Microsatellite instability analysis. A multicenter study for reliability and quality control", Cancer Res, 57, pp.4739~4743 (1997)
  18. Tirkkonen M, "Molecular cytogenetics of primary brest cancer by CGH", Genes Chromosom Cancer, 21, pp.177~184 (1998)
  19. Zenklusen JC, "Frequent loss of heterozygosity in human primary squamous cell and colon carcinomas at 7q31.1:evidence for a broad range tumor suppressor gene", Cancer Res, 55, pp.1347~1350 (1995)
  20. 배병구, "결장직장암에서 수술 전 혈청 CEA와 CA 19-9 측정의 예후적 가치", Annals of Coloproctolgy, 23(5), pp.338~343 (2007), 대한대장항문학회
  21. 송상현, "림프절 전이가 없는 결직장암에서 p27kip1 의 예후인자로서의 역할", Annals of Coloproctolgy, 23(1), pp.34~40 (2007), 대한대장항문학회
  22. 윤용식, "건강증진센터에서 진단된 대장암의 특징", Annals of Coloproctolgy, 23(5), pp.321~326 (2007), 대한대장항문학회
  23. 최평화, "서울아산병원에서 최근 15년간 대장암의 임상 및 병리적 특성의 변화", Annals of Coloproctolgy, 22(6), pp.387~395 (2006), 대한대장항문학회

관련 논문AI추천

이 간행물의 다른 논문 (13건)