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冯·希佩尔-林道肿瘤抑制基因大鼠同源物的克隆及其在大鼠肾细胞癌中的非体细胞突变

Cloning of the rat homologue of the von Hippel-Lindau tumor suppressor gene and its non-somatic mutation in rat renal cell carcinomas.

作者信息

Kikuchi Y, Kobayashi E, Nishizawa M, Hamazaki S, Okada S, Hino O

机构信息

Department of Experimental Pathology, Cancer Institute, Tokyo.

出版信息

Jpn J Cancer Res. 1995 Oct;86(10):905-9. doi: 10.1111/j.1349-7006.1995.tb02999.x.

DOI:10.1111/j.1349-7006.1995.tb02999.x
PMID:7493907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5920593/
Abstract

Recently, von Hippel-Lindau (VHL) gene mutations were detected in non-inherited, sporadic human renal cell carcinomas (RCs) at a high frequency. In order to determine whether or not the VHL gene is also a critical gene in rat RCs, we cloned and sequenced the rat homologue of human VHL gene and searched for mutations of the VHL gene in rat RCs. Mutations in the VHL gene were not detected in spontaneous RCs of the Eker rat model or in ferric nitrilotriacetate-induced rat RCs using the polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) method. These data indicate that mutation of the VHL tumor suppressor gene is not an event in rat renal carcinogenesis, at least in our present systems.

摘要

最近,在非遗传性散发性人类肾细胞癌(RC)中高频检测到冯·希佩尔-林道(VHL)基因突变。为了确定VHL基因在大鼠RC中是否也是关键基因,我们克隆并测序了人类VHL基因的大鼠同源物,并在大鼠RC中寻找VHL基因的突变。使用聚合酶链反应-单链构象多态性(PCR-SSCP)方法,在Eker大鼠模型的自发性RC或次氮基三乙酸铁诱导的大鼠RC中未检测到VHL基因突变。这些数据表明,至少在我们目前的系统中,VHL肿瘤抑制基因突变不是大鼠肾癌发生过程中的一个事件。

相似文献

1
Cloning of the rat homologue of the von Hippel-Lindau tumor suppressor gene and its non-somatic mutation in rat renal cell carcinomas.冯·希佩尔-林道肿瘤抑制基因大鼠同源物的克隆及其在大鼠肾细胞癌中的非体细胞突变
Jpn J Cancer Res. 1995 Oct;86(10):905-9. doi: 10.1111/j.1349-7006.1995.tb02999.x.
2
Somatic mutation of the tuberous sclerosis (Tsc2) tumor suppressor gene in chemically induced rat renal carcinoma cell.化学诱导的大鼠肾癌细胞中结节性硬化症(Tsc2)肿瘤抑制基因的体细胞突变。
J Urol. 1997 Jul;158(1):275-8. doi: 10.1097/00005392-199707000-00085.
3
Renal cell carcinoma development in the rat independent of alterations at the VHL gene locus.大鼠肾细胞癌的发展与VHL基因位点的改变无关。
Mol Carcinog. 1996 Feb;15(2):154-61. doi: 10.1002/(SICI)1098-2744(199602)15:2<154::AID-MC8>3.0.CO;2-J.
4
Development of high-grade renal cell carcinomas in rats independently of somatic mutations in the Tsc2 and VHL tumor suppressor genes.大鼠高级别肾细胞癌的发生独立于Tsc2和VHL肿瘤抑制基因的体细胞突变。
Jpn J Cancer Res. 1998 Aug;89(8):814-20. doi: 10.1111/j.1349-7006.1998.tb00633.x.
5
Biallelic mutations of the Tsc2 gene in chemically induced rat renal cell carcinoma.化学诱导的大鼠肾细胞癌中Tsc2基因的双等位基因突变。
Int J Cancer. 1998 Sep 11;77(6):895-900. doi: 10.1002/(sici)1097-0215(19980911)77:6<895::aid-ijc16>3.0.co;2-0.
6
Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma.冯·希佩尔-林道肿瘤抑制基因的种系突变与散发性肾细胞癌中的体细胞冯·希佩尔-林道畸变相似。
Am J Hum Genet. 1994 Dec;55(6):1092-102.
7
Polymerase chain reaction-single-strand conformation polymorphism analysis for the VHL gene in chemically induced kidney tumors of rats using intron-derived primers.使用内含子衍生引物对大鼠化学诱导肾肿瘤中VHL基因进行聚合酶链反应-单链构象多态性分析。
Mol Carcinog. 1997 Aug;19(4):230-5.
8
Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation. A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGH.在一个发生新生突变的家族中检测到冯·希佩尔-林道肿瘤抑制基因的种系突变和体细胞纯合缺失。一项包括细胞遗传学、聚合酶链反应/单链构象多态性分析、荧光原位杂交和比较基因组杂交的联合遗传学研究。
Hum Genet. 1996 Jun;97(6):770-6. doi: 10.1007/BF02346188.
9
Von Hippel-Lindau disease and sporadic renal cell carcinoma.冯·希佩尔-林道病与散发性肾细胞癌。
Cancer Surv. 1995;25:219-32.
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Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis.原发性肾细胞癌中冯·希佩尔-林道(VHL)肿瘤抑制基因的失活及3号染色体短臂的等位基因缺失:透明细胞肾肿瘤发生中存在不依赖VHL途径的证据
Genes Chromosomes Cancer. 1998 Jul;22(3):200-9. doi: 10.1002/(sici)1098-2264(199807)22:3<200::aid-gcc5>3.0.co;2-#.

引用本文的文献

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Cancers (Basel). 2022 Mar 15;14(6):1495. doi: 10.3390/cancers14061495.
2
Choosing The Right Animal Model for Renal Cancer Research.为肾癌研究选择合适的动物模型。
Transl Oncol. 2020 Mar;13(3):100745. doi: 10.1016/j.tranon.2020.100745. Epub 2020 Feb 22.
3
cAMP-dependent cytosolic mislocalization of p27(kip)-cyclin D1 during quinol-thioether-induced tuberous sclerosis renal cell carcinoma.喹喔啉硫醚诱导的结节性硬化症肾细胞癌中 p27(kip)-cyclin D1 依赖 cAMP 的胞质定位错误
Toxicol Sci. 2011 Aug;122(2):361-71. doi: 10.1093/toxsci/kfr118. Epub 2011 Jun 20.
4
Specific allelic loss of p16 (INK4A) tumor suppressor gene after weeks of iron-mediated oxidative damage during rat renal carcinogenesis.大鼠肾癌发生过程中,在铁介导的氧化损伤数周后,p16(INK4A)肿瘤抑制基因出现特异性等位基因缺失。
Am J Pathol. 2002 Feb;160(2):419-24. doi: 10.1016/S0002-9440(10)64860-2.
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A novel "Nihon" rat model of a Mendelian dominantly inherited renal cell carcinoma.一种新型的孟德尔显性遗传性肾细胞癌“日本”大鼠模型。
Jpn J Cancer Res. 2000 Nov;91(11):1096-9. doi: 10.1111/j.1349-7006.2000.tb00890.x.
6
Development of high-grade renal cell carcinomas in rats independently of somatic mutations in the Tsc2 and VHL tumor suppressor genes.大鼠高级别肾细胞癌的发生独立于Tsc2和VHL肿瘤抑制基因的体细胞突变。
Jpn J Cancer Res. 1998 Aug;89(8):814-20. doi: 10.1111/j.1349-7006.1998.tb00633.x.

本文引用的文献

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