Department of Molecular Biology, Pasteur Institute of Iran, Tehran, Iran.
Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Cancer Rep (Hoboken). 2023 Feb;6(2):e1722. doi: 10.1002/cnr2.1722. Epub 2022 Oct 23.
In Iran, the delay in diagnosis and treatment of breast cancer results in low survival rates.
It is essential to characterize new therapeutic targets and prognostic breast cancer biomarkers. The rising evidence suggested that long non-coding RNAs (lncRNAs) expression levels are deregulated in human cancers and can use as biomarkers for the rapid diagnosis of breast cancer.
In the present study, a quantitative real-time polymerase chain reaction (qRT-PCR) technique was used to measure 20 oncogenic and tumor suppressor lncRNAs expression levels in whole blood samples of female breast cancer patients and healthy women. Receiver operating characteristic curve (ROC) was used to assess the diagnostic value of each selected lncRNA as a biomarker.
The results revealed that some circulating lncRNAs (MEG3, NBAT1, NKILA, GAS5, EPB41L4A-AS2, Z38, and BC040587) were significantly down-regulated in breast cancer patients compared to healthy women. In contrast, other circulating lncRNAs (H19, SPRY4-IT1, XIST, UCA1, AC026904.1, CCAT1, CCAT2, ITGB2-AS, and AK058003) were significantly up-regulated in breast cancer patients compared to controls. It was shown that the expression levels of NKILA, and NBAT1 lncRNAs were related to tumor size, and BC040587 expression level related to age, node metastasis, tumor size, and grade (p < .05). The association between H19 and SPRY4-IT1 lncRNAs with HER-2 was confirmed statistically (p < .05). ROC curves illustrated that the blood levels of SPRY4-IT1, XIST, and H19 lncRNAs have excellent potential in discriminating breast cancer from the healthy controls, showing an AUC of 1.0 (95% CI 1.0-1.0, p = .00), 0.898 (95% CI 0.815-0.981, p = .00), and 0.848 (95% CI 0.701-0.995, p = .01), respectively.
In conclusion, the expression levels of circulating H19 and SPRY4-IT1 lncRNAs in breast cancer patients could consider as the prognostic biomarkers and therapeutic targets in breast cancer, because of their excellent power in discriminating breast cancer from healthy individuals and the significant correlation of H19, and SPRY4-IT1 lncRNAs with clinicopathological traits. We also suggest the possible application of BC040587 lncRNA as a diagnostic and prognostic indicator to assess tumor progression in case of verification in larger patients' cohorts.
在伊朗,乳腺癌的诊断和治疗延误导致生存率较低。
描述新的治疗靶点和乳腺癌预后生物标志物至关重要。越来越多的证据表明,长链非编码 RNA(lncRNA)在人类癌症中的表达水平失调,可以用作乳腺癌快速诊断的生物标志物。
在本研究中,使用定量实时聚合酶链反应(qRT-PCR)技术测量了 20 种致癌和肿瘤抑制 lncRNA 在女性乳腺癌患者和健康女性全血样本中的表达水平。接收者操作特征曲线(ROC)用于评估每个选定 lncRNA 作为生物标志物的诊断价值。
结果显示,与健康女性相比,一些循环 lncRNA(MEG3、NBAT1、NKILA、GAS5、EPB41L4A-AS2、Z38 和 BC040587)在乳腺癌患者中显著下调。相比之下,与对照组相比,其他循环 lncRNA(H19、SPRY4-IT1、XIST、UCA1、AC026904.1、CCAT1、CCAT2、ITGB2-AS 和 AK058003)在乳腺癌患者中显著上调。结果表明,NKILA 和 NBAT1 lncRNA 的表达水平与肿瘤大小有关,BC040587 的表达水平与年龄、淋巴结转移、肿瘤大小和分级有关(p<0.05)。H19 和 SPRY4-IT1 lncRNA 与 HER-2 的相关性得到了统计学证实(p<0.05)。ROC 曲线表明,SPRY4-IT1、XIST 和 H19 lncRNA 的血液水平在区分乳腺癌与健康对照组方面具有出色的潜力,AUC 分别为 1.0(95%CI 1.0-1.0,p=0.00)、0.898(95%CI 0.815-0.981,p=0.00)和 0.848(95%CI 0.701-0.995,p=0.01)。
总之,乳腺癌患者循环 H19 和 SPRY4-IT1 lncRNA 的表达水平可以作为乳腺癌的预后生物标志物和治疗靶点,因为它们在区分乳腺癌与健康个体方面具有出色的能力,并且 H19 和 SPRY4-IT1 lncRNA 与临床病理特征具有显著相关性。我们还建议将 BC040587 lncRNA 作为诊断和预后指标进行进一步研究,以评估肿瘤的进展。