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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Tumor-specific mutation and downregulation of ING5 detected in oral squamous cell carcinoma.
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Tumor-specific mutation and downregulation of ING5 detected in oral squamous cell carcinoma.

机译:在口腔鳞状细胞癌中检测到肿瘤特异性突变和ING5下调。

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摘要

Our previous study showed high frequency of allelic loss at chromosome 2q37 region in oral cancer. This location contains several candidate tumor suppressor genes such as PPP1R7, ILKAP, DTYMK and ING5. We previously showed 3 members of inhibitor of growth (ING) family, ING1, ING3 and ING4 as tumor suppressor gene in head and neck cancer. As ING5 shows high homology with other members of ING genes including highly conserved carboxy-terminal plant homeodomain and nuclear localization signal, we first picked up ING5 and examined it as a possible tumor suppressor in oral cancer. For this aim, mutation and mRNA expression status of ING5 in paired normal and oral squamous cell carcinoma samples were examined by reverse transcription polymerase chain reaction (RT-PCR) and sequencing. Three missense mutations located within leucine zipper like (LZL) finger and novel conserved region (NCR) domains in ING5 protein were detected, probably abrogating its normal function. We also found 5 different alternative splicing variants of ING5. Then, we examined mRNA level of ING5 by quantitative real time reverse transcription polymerase chain reaction (qRT-PCR) analysis, which demonstrated decreased expression of ING5 mRNA in 61% of the primary tumors as compared to the matched normal samples. In conclusion, tumor-specific mutation and downregulation of ING5 mRNA suggested it as a tumor suppressor gene in oral squamous cell carcinoma.
机译:我们先前的研究显示口腔癌中2q37号染色体区域的等位基因丢失频率很高。该位置包含几个候选肿瘤抑制基因,例如PPP1R7,ILKAP,DTYMK和ING5。先前我们显示了3个生长抑制因子(ING)家族成员ING1,ING3和ING4作为头颈癌的肿瘤抑制基因。由于ING5与ING基因的其他成员(包括高度保守的羧基末端植物同源结构域和核定位信号)具有高度同源性,因此我们首先选择了ING5,并将其检测为口腔癌的一种可能的抑癌基因。为此,通过逆转录聚合酶链反应(RT-PCR)和测序检查了成对的正常和口腔鳞状细胞癌样品中ING5的突变和mRNA表达状态。检测到位于亮氨酸拉链样(LZL)手指和ING5蛋白中新的保守区(NCR)域内的三个错义突变,可能废除了其正常功能。我们还发现了ING5的5种不同的可变剪接变体。然后,我们通过定量实时逆转录聚合酶链反应(qRT-PCR)分析检查了ING5的mRNA水平,这表明与匹配的正常样品相比,在61%的原发肿瘤中ING5 mRNA的表达下降。总之,ING5 mRNA的肿瘤特异性突变和下调表明它是口腔鳞状细胞癌的抑癌基因。

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