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Two new mutations and three novel polymorphisms in the RB1 gene in Ecuadorian patients.

作者信息

Leone Paola E, Vega María Elena, Jervis Paola, Pestaña Angel, Alonso Javier, Paz-Y-Miño César

机构信息

Laboratorio de Genética Molecular y Citogenética Humana, Escuela de Ciencias Biológicas, Pontificia Universidad Católica del Ecuador, PO Box 17-1-2184, Quito, Ecuador.

Unidad de Genética, Facultad de Medicina, Pontificia Universidad Católica del Ecuador, Quito, Ecuador.

出版信息

J Hum Genet. 2003;48(12):639-641. doi: 10.1007/s10038-003-0092-5. Epub 2003 Nov 19.

DOI:10.1007/s10038-003-0092-5
PMID:14625809
Abstract

RB1 is the gene responsible for retinoblastoma, the most common malignant intraocular tumor of infancy and early childhood. There are no reports about this gene in Ecuadorian populations, and only a few studies have been published in Latin America about this subject. There is a spectrum of more than 370 mutations described in the RB1 gene mutation database (http://www.d-lohmann.de/Rb/mutations.html), and alterations have been found in 25 of the 27 exons. During the exon-by-exon analysis of 31 tumor and blood samples from Ecuadorian patients, we found two new mutations and three novel polymorphisms. One of the polymorphisms is located in intron 26 where no alterations of the gene have been described previously. The polymorphisms were found in all of the patients' tumor samples, but not in normal population, suggesting there might be a relationship between these polymorphisms and the development of retinoblastoma in the Ecuadorian population.

摘要

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本文引用的文献

1
Identification of novel mutations in the RB1 gene in Mexican patients with retinoblastoma.墨西哥视网膜母细胞瘤患者RB1基因新突变的鉴定
Cancer Genet Cytogenet. 2002 Oct 1;138(1):27-31. doi: 10.1016/s0165-4608(02)00577-0.
2
A novel missense mutation in patients from a retinoblastoma pedigree showing only mild expression of the tumor phenotype.来自一个视网膜母细胞瘤家系的患者中发现一种新型错义突变,该家系仅表现出肿瘤表型的轻度表达。
Oncogene. 1998 Jun 18;16(24):3211-3. doi: 10.1038/sj.onc.1201833.
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Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.
Mol Genet Genomic Med. 2015 Dec 21;4(1):9-17. doi: 10.1002/mgg3.192. eCollection 2016 Jan.
4
Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification.使用多重连接依赖探针扩增技术对伊朗视网膜母细胞瘤患者的RB1基因进行大片段重排筛查。
Mol Vis. 2013;19:454-62. Epub 2013 Feb 22.
5
Genotyping of Polymorphic Microsatellite Markers Linked to RB1 Locus in Iranian Population.伊朗人群中与RB1基因座相关的多态性微卫星标记的基因分型
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孤立性单侧视网膜母细胞瘤患者的体质性RB1基因突变
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The spectrum of RB1 germ-line mutations in hereditary retinoblastoma.遗传性视网膜母细胞瘤中RB1种系突变的谱系
Am J Hum Genet. 1996 May;58(5):940-9.
5
Mortality from second tumors among long-term survivors of retinoblastoma.视网膜母细胞瘤长期幸存者中二次肿瘤导致的死亡率。
J Natl Cancer Inst. 1993 Jul 21;85(14):1121-8. doi: 10.1093/jnci/85.14.1121.
6
Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma.视网膜母细胞瘤中RB1等位基因高甲基化的频率及亲本来源
Hum Genet. 1994 Nov;94(5):491-6. doi: 10.1007/BF00211013.
7
Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma.RB1基因种系突变谱:对232例遗传性和非遗传性视网膜母细胞瘤患者的研究
Hum Mol Genet. 1995 Mar;4(3):383-8. doi: 10.1093/hmg/4.3.383.
8
Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma.RB1基因中CGA-精氨酸密码子频繁发生的由胞嘧啶到胸腺嘧啶的基因组成突变,在双侧(遗传性)视网膜母细胞瘤患者中产生过早的终止密码子。
Eur J Hum Genet. 1994;2(4):281-90. doi: 10.1159/000472372.
9
Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastoma.阿根廷散发性双侧视网膜母细胞瘤家族中RB1种系突变的鉴定。
J Med Genet. 1995 Jun;32(6):475-9. doi: 10.1136/jmg.32.6.475.
10
Mutation and cancer: statistical study of retinoblastoma.突变与癌症:视网膜母细胞瘤的统计学研究
Proc Natl Acad Sci U S A. 1971 Apr;68(4):820-3. doi: 10.1073/pnas.68.4.820.