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克什米尔人群膀胱移行细胞癌中活化H-ras基因突变

Activated H-ras gene mutations in transitional cell carcinoma of urinary bladder in a Kashmiri population.

作者信息

Pandith Arshad Ahmad, Shah Zafar, Rasool Roohi, Yousuf Adfar, Parveen Nighat, Wani Saleem, Siddiqi Mushtaq

机构信息

Department of Immunology and Molecular Medicine, Sher-I-Kashmir Institute of Medical Sciences, Soura, Srinagar, Kashmir, India.

出版信息

Tumori. 2010 Nov-Dec;96(6):993-8.

Abstract

AIMS AND BACKGROUND

The primary aim of the study was to evaluate the incidence of H-ras specific point mutations among a group of Kashmiri patients diagnosed with bladder cancer. We also explored the correlation of clinic-pathological status of the illness with these mutations.

METHODS AND STUDY DESIGN

The DNA samples of both tumor and normal tissue were evaluated for the occurrence of H-ras activating mutations in exon 1 and 2 by PCR-SCCP and DNA sequencing. In addition, blood was also collected from all the cases to rule out any germ-line mutation.

RESULTS

Point mutations of activated H-ras identified in bladder cancer patients were 14.5% (7 of 48), including four transversions (two G-->T and two A-->T) and three transitions (A-->G). Of the mutations, 71.4% were detected in codon 61 and 28.6% in codon 12. The pattern of mutation in the study showed a significant association with smoking in bladder tumors (P < 0.05). No correlation was found between tumor grade and/or stage and the presence of H-ras mutation.

CONCLUSIONS

Activation of H-ras by mutation plays a less frequent role than other genetic events in the development of the most transitional cell tumors of the bladder in Kashmiri population.

摘要

目的与背景

本研究的主要目的是评估一组被诊断为膀胱癌的克什米尔患者中H-ras特异性点突变的发生率。我们还探讨了该疾病的临床病理状态与这些突变之间的相关性。

方法与研究设计

通过聚合酶链反应-单链构象多态性分析(PCR-SCCP)和DNA测序,评估肿瘤组织和正常组织的DNA样本中第1和第2外显子中H-ras激活突变的发生情况。此外,还采集了所有病例的血液样本以排除任何种系突变。

结果

在膀胱癌患者中鉴定出的激活型H-ras点突变率为14.5%(48例中有7例),包括4种颠换(2个G→T和2个A→T)和3种转换(A→G)。其中,71.4%的突变发生在密码子61,28.6%发生在密码子12。研究中的突变模式显示与膀胱肿瘤中的吸烟有显著相关性(P < 0.05)。未发现肿瘤分级和/或分期与H-ras突变的存在之间存在相关性。

结论

在克什米尔人群中,突变导致的H-ras激活在大多数膀胱移行细胞肿瘤的发生中所起的作用比其他遗传事件要小。

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