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MOLECULAR-GENETIC PROFILES OF COLITIS-ASSOCIATED NEOPLASMS
被引:142
作者
:
KERN, SE
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
KERN, SE
[
1
]
REDSTON, M
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
REDSTON, M
[
1
]
SEYMOUR, AB
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
SEYMOUR, AB
[
1
]
CALDAS, C
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
CALDAS, C
[
1
]
POWELL, SM
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
POWELL, SM
[
1
]
KORNACKI, S
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
KORNACKI, S
[
1
]
KINZLER, KW
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
KINZLER, KW
[
1
]
机构
:
[1]
JOHNS HOPKINS UNIV, SCH MED, CTR ONCOL, BALTIMORE, MD USA
来源
:
GASTROENTEROLOGY
|
1994年
/ 107卷
/ 02期
关键词
:
D O I
:
10.1016/0016-5085(94)90167-8
中图分类号
:
R57 [消化系及腹部疾病];
学科分类号
:
摘要
:
Background/Aims: A major long-term risk for patients with chronic idiopathic colitis is the development of colorectal dysplasia and adenocarcinoma. The presence or absence of specific genetic changes in these lesions will provide important insights into the relationship of colitis-associated dysplasia and the development of carcinoma. Methods: A case-study approach was used to develop detailed molecular genetic profiles of advanced dysplasias and carcinomas from six patients with ulcerative colitis or Crohn's colitis. Results: Numerous genetic alterations were identified in each of the dysplasias and carcinomas profiled. These genetic alterations involved many of the same targets found in sporadic colorectal tumors and included multiple sites of allelic deletion, microsatellite instabilities, and mutations of the K-ras, p53, and APC genes. The progression of dysplasia to carcinoma was often accompanied by an accumulation of these mutations. Conclusions: Genetic alterations are common in colitis-associated neoplasia, just as in sporadic colorectal neoplasia. This could have important implications for the evaluation and treatment of patients with colitis. © 1994.
引用
收藏
页码:420 / 428
页数:9
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0
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