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人原发性浅表性膀胱癌中p16/MTS1的体细胞改变不常见。

Infrequent somatic alteration of p16/MTS1 in human primary superficial bladder cancers.

作者信息

Okajima E, Fukuda T, Okita S, Tsutsumi M, Hirao Y, Okajima E, Konishi Y

机构信息

Department of Oncological Pathology, Nara Medical University, Japan.

出版信息

Cancer Lett. 1996 Jun 5;103(2):227-31. doi: 10.1016/0304-3835(96)04225-5.

DOI:10.1016/0304-3835(96)04225-5
PMID:8635161
Abstract

Although superficial bladder cancer, usually presenting as low grade transitional cell carcinomas, are easily resected by transurethral intervention, their frequent recurrence and progression of satage or grade of the recurrent tumors in some cases is a major problem in urology. Deletion of chromosome 9, bands 9p21-22 in bladder cancers including the lowest grade and stage, suggest potential location of candidate tumor suppressor genes. Recently, p16/MTS1 was isolated from 9p21-22 as a multiple tumor suppressor gene, which regulates the cyclin dependent kinase 4 in the G1/S phase of the cell cycle. In the present study, somatic alterations of p16/MTS1 were examined concentrating on histologically defined superficial bladder carcinomas by polymerase chain reaction (PCR)-single strand conformation polymorphism (SSCP) technique using paraffin embedded materials. Infrequent alterations of p16/MTS1 in superficial bladder cancers, one deletion and one silent mutation in 15 cases, were detected. The results suggest that p16/MTS1 mutation is not involved in the development of superficial urinary bladder carcinomas.

摘要

尽管浅表性膀胱癌通常表现为低级别移行细胞癌,可通过经尿道干预轻松切除,但它们频繁复发以及某些情况下复发肿瘤的分期或分级进展是泌尿外科的一个主要问题。在包括最低级别和分期的膀胱癌中,9号染色体9p21 - 22带的缺失提示候选肿瘤抑制基因的潜在定位。最近,p16/MTS1从9p21 - 22中分离出来,作为一种多肿瘤抑制基因,它在细胞周期的G1/S期调节细胞周期蛋白依赖性激酶4。在本研究中,使用石蜡包埋材料,通过聚合酶链反应(PCR)-单链构象多态性(SSCP)技术,集中研究组织学定义的浅表性膀胱癌中p16/MTS1的体细胞改变。在浅表性膀胱癌中检测到p16/MTS1的改变不常见,15例中有1例缺失和1例沉默突变。结果表明p16/MTS1突变不参与浅表性膀胱癌的发生发展。

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1
Infrequent somatic alteration of p16/MTS1 in human primary superficial bladder cancers.人原发性浅表性膀胱癌中p16/MTS1的体细胞改变不常见。
Cancer Lett. 1996 Jun 5;103(2):227-31. doi: 10.1016/0304-3835(96)04225-5.
2
Frequent p16/MTS1 inactivation in early stages of urothelial carcinoma of the bladder is not associated with tumor recurrence.膀胱尿路上皮癌早期阶段常见的p16/MTS1失活与肿瘤复发无关。
Eur Urol. 2001 Nov;40(5):518-24. doi: 10.1159/000049829.
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Infrequent somatic mutation of the MTS1 gene in primary bladder carcinomas.原发性膀胱癌中MTS1基因的罕见体细胞突变。
Jpn J Cancer Res. 1995 Mar;86(3):249-51. doi: 10.1111/j.1349-7006.1995.tb03047.x.
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Deletion of the p16 and p15 genes in human bladder tumors.人类膀胱肿瘤中p16和p15基因的缺失。
J Natl Cancer Inst. 1995 Oct 18;87(20):1524-9. doi: 10.1093/jnci/87.20.1524.
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Infrequent somatic mutations of the p16 and p15 genes in human bladder cancer: p16 mutations occur only in low-grade and superficial bladder cancers.人膀胱癌中p16和p15基因的罕见体细胞突变:p16突变仅发生在低级别和表浅性膀胱癌中。
Oncol Res. 1995;7(7-8):327-30.
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Decreased expression of the p16/MTS1 gene without mutation is frequent in human urinary bladder carcinomas.在人类膀胱癌中,p16/MTS1基因表达降低且无突变的情况很常见。
Jpn J Clin Oncol. 1997 Feb;27(1):22-5. doi: 10.1093/jjco/27.1.22.
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Genetic evidence in melanoma and bladder cancers that p16 and p53 function in separate pathways of tumor suppression.黑色素瘤和膀胱癌中的遗传学证据表明,p16和p53在不同的肿瘤抑制途径中发挥作用。
Am J Pathol. 1995 May;146(5):1199-206.
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Growth arrest and suppression of tumorigenicity of bladder-carcinoma cell lines induced by the P16/CDKN2 (p16INK4A, MTS1) gene and other loci on human chromosome 9.P16/CDKN2(p16INK4A,MTS1)基因及人类9号染色体上其他位点诱导膀胱癌细胞系生长停滞并抑制其致瘤性
Int J Cancer. 1996 Mar 15;65(6):840-6. doi: 10.1002/(SICI)1097-0215(19960315)65:6<840::AID-IJC22>3.0.CO;2-6.
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Increased p16 levels correlate with pRb alterations in human urothelial cells.人尿路上皮细胞中p16水平升高与视网膜母细胞瘤蛋白(pRb)改变相关。
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p16 (CDKN2) is a major deletion target at 9p21 in bladder cancer.p16(细胞周期蛋白依赖性激酶抑制剂2)是膀胱癌中9p21位点的主要缺失靶点。
Hum Mol Genet. 1995 Sep;4(9):1569-77. doi: 10.1093/hmg/4.9.1569.

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Analysis of p53, p16MTS, p21WAF1 and H-ras in archived bladder tumours from workers exposed to aromatic amines.
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The CDKN2A (p16) gene and human cancer.CDKN2A(p16)基因与人类癌症。
Mol Med. 1997 Jan;3(1):5-20.