CONCLUSION:Our findings show that copy number loss of FHIT is associated with lymph node metastasis (LNM) and suggest that the down-regulation of Fhit indicates poor prognosis in early oral squamous cell carcinoma (OSCC). OBJECTIVES:The purpose of this study was to identify alterations in genetic markers related to LNM in early OSCC. METHODS:Genome-wide copy number alterations were analyzed in 14 early OSCCs with (n = 7) or without (n = 7) cervical LNM using 180K array-comparative genomic hybridization. To explore the prognostic implications of the most significantly associated genetic alteration with cervical LNM, immunohistochemical analysis was conducted in 30 OSCCs. RESULTS:A total of 11 recurrently altered regions (RARs) were identified in the 14 OSCC cases. Six RARs on chromosomes 3p26-3p14, 5q22, and 9p21 were found to be significantly more common in early OSCC with LNM (p < 0.05). Among these, loss of 3p14.2 (where the FHIT gene is located) was the most frequent (five of seven patients with LNM, and none of seven without LNM), and most significantly associated with cervical LNM (p = 0.005). Fhit immunohistochemical staining of 30 OSCCs showed that Fhit negativity was associated with cervical LNM (p = 0.032) and poor disease-specific survival (p = 0.045).

译文

结论:我们的研究结果表明,FHIT的拷贝数丢失与淋巴结转移(LNM)有关,并且表明Fhit的下调表明早期口腔鳞状细胞癌(OSCC)的预后不良。
目的:本研究的目的是鉴定早期OSCC中与LNM相关的遗传标记的变化。
方法:采用180K阵列比较基因组杂交技术,分析了14例有(n = 7)有或无(n = 7)宫颈LNM的早期OSCC中全基因组拷贝数的变化。为了探讨与宫颈LNM最显着相关的遗传改变的预后意义,在30个OSCC中进行了免疫组织化学分析。
结果:在14例OSCC病例中共鉴定出11个反复改变的区域(RAR)。发现在LNM的早期OSCC中,染色体3p26-3p14、5q22和9p21上的六个RAR更为常见(p <0.05)。其中,3p14.2(FHIT基因所在的位置)的丢失最为频繁(7名LNM患者中有5名,而没有LNM的7名患者中没有一个),并且与宫颈LNM相关性最高(p = 0.005)。对30个OSCC进行Fhit免疫组织化学染色显示Fhit阴性与宫颈LNM(p = 0.032)和较差的疾病特异性存活率(p = 0.045)相关。

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