CD44基因在乳腺病变细针抽吸细胞中表达的聚合酶链反应。

J Bolodeoku, K Yoshida, P Yeomans, C A Wells, D Tarin
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引用次数: 6

摘要

目的:探讨研究临床病变细针抽吸液中特异性基因表达的可行性。利用逆转录/聚合酶链反应(RT-PCR)技术,从乳腺疾病门诊患者的诊断性细针抽吸液中证实CD44基因在细胞中的表达。方法:对41例乳腺病变患者进行细针抽吸细胞学诊断后,从注射器桶内剩余细胞中提取聚腺苷化RNA。利用变异外显子插入位点的引物进行RT-PCR分析CD44基因的表达。所得产物在1.2%琼脂糖凝胶上分离,用Southern blotting转移到尼龙膜上,并用特异性探针杂交该基因的标准(组成)和变异外显子。结果:在与CD44标准外显子探针杂交时,在所检测的41个样本中有22个样本显示了大约482个碱基对的预期扩增产物。用“变异”外显子探针(外显子7 (v2)、8 (v3)、9b (v4)、12 (v7)和15 (v10))对其中12个样本进行进一步杂交,发现所有这些样本中都存在大分子变异。然而,用探针检测到的外显子7 (v2)、8 (v3)和9b (v4)的表达模式在患者之间存在差异。结论:采用RT-PCR技术证实了细针抽吸后留在注射器中的细胞中CD44基因的标准区和变异区表达。5'变异外显子探针似乎在患者中表现出不同的表达模式。目前正在进行进一步的研究,以确定该基因的各种成分的表达与细胞学诊断之间是否存在任何相关性。使用这种方法,将有可能研究其他候选标记基因在乳腺癌中使用细针抽吸的表达。
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Demonstration of CD44 gene expression in cells from fine needle aspirates of breast lesions by the polymerase chain reaction.

Aim-To demonstrate the feasibility of studying specific gene expression in fine needle aspirates from clinical lesions. The reverse transcription/polymerase chain reaction (RT-PCR) technique was used to demonstrate CD44 gene expression in cells from diagnostic fine needle aspirates taken from patients attending the outpatient clinic for breast diseases.Methods-Polyadenylated RNA was extracted from the cells remaining in the syringe barrel after fine needle aspirate cytological diagnosis of 41 patients with breast lesions. Analysis of CD44 gene expression was performed by RT-PCR using primers flanking the site for insertion of the variant exons. The resulting products were separated on 1.2% agarose gels, transferred to nylon membranes using Southern blotting and hybridised with specific probes for standard (constitutive) and variant exons of this gene.Results-On hybridisation with the CD44 standard exon probe, the expected amplified product of approximately 482 base pairs was visualised in 22 of 41 samples examined. Further hybridisation with the "variant" exon probes (exons 7 (v2), 8 (v3), 9b (v4), 12 (v7), and 15 (v10)) on 12 of these samples showed the presence of large molecular variants in all of these samples. However, the expression pattern detected with the probes for exons 7 (v2), 8 (v3) and 9b (v4) differed among the patients.Conclusions-Expression of the standard and variant regions of the CD44 gene in cells remaining in the syringe after fine needle aspiration was demonstrated using RT-PCR. The 5' variant exon probes seemed to show different patterns of expression among the patients. Further studies are currently being conducted to determine whether there is any correlation between expression of the various components of this gene and cytological diagnosis. Using this method, it would be possible to study the expression of other candidate marker genes in breast cancer using fine needle aspirates.

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