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Evaluation of the FHIT gene in colorectal cancers.

作者信息

Thiagalingam S, Lisitsyn N A, Hamaguchi M, Wigler M H, Willson J K, Markowitz S D, Leach F S, Kinzler K W, Vogelstein B

机构信息

The Johns Hopkins Oncology Center, Baltimore, Maryland 21231, USA.

出版信息

Cancer Res. 1996 Jul 1;56(13):2936-9.

PMID:8674044
Abstract

A variety of studies suggests that tumor suppressor loci on chromosome 3p are important in various forms of human neoplasia. Recently, a chromosome 3p14.2 gene called FHIT was discovered and proposed as a candidate tumor suppressor gene in colorectal and other cancers. We evaluated the FHIT gene in a panel of colorectal cancer cell lines and xenografts, which allowed a comprehensive mutational analysis. A transcript containing the complete coding sequence was found to be expressed at robust levels in 29 of 31 cancers tested. The complete sequence of the coding region of the gene was determined and found to be normal in all 29 of these cases. These studies suggest either that FHIT is inactivated by an unusual mechanism or that it plays a role in relatively few colorectal tumors.

摘要

相似文献

1
Evaluation of the FHIT gene in colorectal cancers.
Cancer Res. 1996 Jul 1;56(13):2936-9.
2
Deletion of the FHIT gene in human colorectal cancer is independent of high-risk HPV infection.人类结直肠癌中FHIT基因的缺失与高危型人乳头瘤病毒感染无关。
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3
Frequent abnormalities of FHIT, a candidate tumor suppressor gene, in head and neck cancer cell lines.候选抑癌基因FHIT在头颈癌细胞系中频繁出现异常。
Cancer Res. 1996 Nov 15;56(22):5128-31.
4
FHIT and FRA3B 3p14.2 allele loss are common in lung cancer and preneoplastic bronchial lesions and are associated with cancer-related FHIT cDNA splicing aberrations.FHIT和FRA3B 3p14.2等位基因缺失在肺癌和癌前支气管病变中很常见,并且与癌症相关的FHIT cDNA剪接异常有关。
Cancer Res. 1997 Jun 1;57(11):2256-67.
5
Analysis of the FHIT gene and FRA3B region in sporadic breast cancer, preneoplastic lesions, and familial breast cancer probands.散发性乳腺癌、癌前病变及家族性乳腺癌先证者中FHIT基因与FRA3B区域的分析
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FHIT gene and the FRA3B region are not involved in the genetics of renal cell carcinomas.脆性组氨酸三联体(FHIT)基因和FRA3B区域不参与肾细胞癌的遗传学过程。
Genes Chromosomes Cancer. 1997 Sep;20(1):9-15.
7
FHIT gene alterations in esophageal cancer and ulcerative colitis (UC).食管癌和溃疡性结肠炎(UC)中的FHIT基因改变。
Oncogene. 1997 Jul 3;15(1):101-5. doi: 10.1038/sj.onc.1201169.
8
Loss of FHIT expression in cervical carcinoma cell lines and primary tumors.宫颈癌细胞系和原发性肿瘤中FHIT表达缺失。
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Frequent abnormalities of the putative tumor suppressor gene FHIT at 3p14.2 in pancreatic carcinoma cell lines.胰腺癌细胞系中位于3p14.2的假定肿瘤抑制基因FHIT频繁出现异常。
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Inactivation of the human fragile histidine triad gene at 3p14.2 in monochromosomal human/mouse microcell hybrid-derived severe combined immunodeficient mouse tumors.在单染色体人/小鼠微细胞杂交衍生的严重联合免疫缺陷小鼠肿瘤中,位于3p14.2的人类脆性组氨酸三联体基因失活。
Cancer Res. 2000 Dec 15;60(24):7119-25.

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