成纤维细胞生长因子受体2
成纤维细胞生长因子受体3
成纤维细胞生长因子受体
生物
错义突变
外显子
癌症研究
遗传学
突变
成纤维细胞生长因子受体1
成纤维细胞生长因子受体4
阿珀特综合征
分子生物学
颅缝病
成纤维细胞生长因子
基因
受体
作者
Jun‐Hyeog Jang,Kihyuk Shin,Jae-Gahb Park
出处
期刊:PubMed
[National Institutes of Health]
日期:2001-05-01
卷期号:61 (9): 3541-3
被引量:276
摘要
Autosomal dominant disorders of skeletal and cranial development have been linked to fibroblast growth factor receptor (FGFR) 2 and FGFR3. Here we report two identical mutations in FGFR2 that cause craniosynostosis syndromes, Crouzon, Apert, and Pfeiffer in gastric carcinoma. A missense mutation (Ser267Pro) in exon IIIa and a splice site mutation (940-2A-->G) in exon IIIc were detected in gastric cancer patients. Interestingly, these heterozygous somatic mutations are identical to the germinal activating mutations in FGFR2 reported previously in craniosynostosis syndromes. In addition, the two novel mutations of FGFR3 in colorectal carcinomas were identified. All identified mutations occurred at highly conserved sequences, not only in the FGFR family of molecules, but also throughout evolution and clustered in the immunoglobulin-like loop-III domain, highlighting the functional importance of this domain. Our results indicate that FGFR2 and FGFR3, in addition to their potential role in skeletal dysplasias, play an important role in tumorigenesis.
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