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RT-qPCR for PHOX2B mRNA is a highly specific and sensitive method to assess neuroblastoma minimal residual disease in testicular tissue

机译:用于PHOX2B mRNA的RT-qPCR是评估睾丸组织中神经母细胞瘤最小残留病的高度特异性和灵敏的方法

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摘要

Neuroblastoma (NB) is the most common type of extracranial solid tumor in children with a high prevalence in toddlers. For childhood cancer survivors, preservation of reproductive potential is an important factor for quality of life. The optimization of NB minimal residual disease (MRD) detection in testicular tissue is crucial to evaluate the risk of malignant cell reintroduction. The first step in the present study was to assess the accuracy of reverse transcription-quantitative polymerase chain reaction (RT-qPCR) to detect tyrosine hydroxylase (TH), paired-like homeobox 2b (PHOX2B) and doublecortin (DCX) mRNA expression in frozen/thawed testicular tissues of patients with non-obstructive azoospermia (NOA) contaminated (in vitro model) with an increasing number of IMR-32 and SK-N-SH NB cells. Testicular tissues were frozen by slow or snap freezing. The second step was to determine the expression levels of these markers in testicular samples from 4 pre-pubertal males (2 with stage IV NB and 2 with non-NB malignancy). The yield of extracted RNA was similar in testicular samples frozen by slow or snap freezing. In the in vitro model, TH and DCX transcripts were detected in uncontaminated testicular tissues, whereas PHOX2B mRNA was not detected. There was a strong positive association between the number of NB cells used for contamination and PHOX2B transcript levels. For IMR-32 and SK-N-SH NB cell lines, specificity and sensitivity rates of detection were 100% for PHOX2B following in vitro contamination with 10 tumor cells. In testicular samples from pre-pubertal males with and without NB, PHOX2B mRNA expression was not observed, but high expression levels of TH and DCX mRNA were detected, which were similar to expression detected in the in vitro model. Among the markers used in blood and bone marrow for NB MRD studies, the detection of PHOX2B transcripts by RT-qPCR may provide an accurate assessment of NB cells in testicular tissues from males who require fertility preservation.
机译:神经母细胞瘤(NB)是幼儿患病率最高的儿童中最常见的颅外实体瘤类型。对于儿童癌症幸存者而言,保留生殖潜能是生活质量的重要因素。睾丸组织中NB最小残留疾病(MRD)检测的优化对于评估恶性细胞再引入的风险至关重要。本研究的第一步是评估逆转录定量聚合酶链反应(RT-qPCR)检测酪氨酸羟化酶(TH),配对样同源盒2b(PHOX2B)和双皮质素(DCX)mRNA在冷冻中的准确性/ IMF-32和SK-N-SH NB细胞数量增加的非阻塞性无精子症(NOA)污染患者的睾丸组织融化(体外模型)。通过慢速或速冻将睾丸组织冷冻。第二步是确定来自4个青春期前男性(2个处于IV NB期和2个非NB恶性)的睾丸样品中这些标志物的表达水平。在通过慢速或速冻冷冻的睾丸样品中,提取的RNA的产量相似。在体外模型中,在未受污染的睾丸组织中检测到TH和DCX转录本,而未检测到PHOX2B mRNA。用于污染的NB细胞数量与PHOX2B转录水平之间有很强的正相关性。对于IMR-32和SK-N-SH NB细胞系,在体外被10个肿瘤细胞污染后,PHOX2B的检测特异性和灵敏度为100%。在有和没有NB的青春期前男性的睾丸样本中,未观察到PHOX2B mRNA表达,但检测到TH和DCX mRNA的高表达水平,与体外模型中检测到的表达水平相似。在用于NB MRD研究的血液和骨髓中的标记物中,通过RT-qPCR检测PHOX2B转录本可以准确评估需要保留生育能力的雄性睾丸组织中NB细胞。

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