Ghaissani Shabrina S, Kinanti Senja R, Warisman Muhammad A, Fitria N
Research Center for Biotechnology, Indonesian Institute of Sciences (LIPI), Jl Raya Cibinong KM 46, Bogor, West Java, Indonesia.
Division of Surgical Oncology Medical School of M. Djamil Hospital, Andalas University, Jl Perintis Kemerdekaan No. 94, Padang, West Sumatra, Indonesia.
J Genet Eng Biotechnol. 2021 Jan 11;19(1):6. doi: 10.1186/s43141-020-00108-9.
Breast cancer is a disease in which cell grows rapidly forming a mass in the breast. HER2 polymorphisms Ile655Val have been studied as biomarkers for breast cancer and may comprise a risk factor of cardiac toxicity for breast cancer-consuming trastuzumab.
In this study, we developed a simple, low cost, and rapid test to detect polymorphism at HER2 gene using SYBR Green I-based melting curve method.
In this report, we performed allelic discrimination with real-time temperature melting (Tm) Shift SYBR Green I-based melting curve method. The melting profiles of amplified DNA HER-2 Ile655Val and its characteristics were analyzed.
Tm value of HER2 GG and AA alleles were 85 ± 0.14 °C and 82.5 ± 0.23 °C, respectively, while cycle threshold (Ct) value of GG, AG, and AA alleles were 19.6 ± 0.27, 22.5 ± 0.23, 18.6 ± 0.22 correspondingly; furthermore, no template control has shown consisting Ct value at 31.18 ± 0.27. The developed methods' characteristics were optimum annealing at 62 °C and Kappa coefficient value 1 with the mean almost consistent with PCR-sequencing. The coefficient of variability for intra-assay of GG, AG, and AA was in the range of 0.2-1%, while the coefficient of variability for inter-assay for each were in the range 0.7-1%. Further, based on PCR, shelf-life assay has shown stability for 3 months of storage observation.
This approach may be considered as simple, rapid, and low cost supporting the rapid study of HER2 epidemiology. Furthermore, the developed methods potentially facilitate clinicians in dealing with breast cancer patients, especially in considering about the cardiotoxicity effect of trastuzumab.
乳腺癌是一种细胞迅速生长并在乳房中形成肿块的疾病。HER2基因多态性Ile655Val已被作为乳腺癌的生物标志物进行研究,并且可能是乳腺癌患者使用曲妥珠单抗后发生心脏毒性的一个风险因素。
在本研究中,我们开发了一种简单、低成本且快速的检测方法,使用基于SYBR Green I的熔解曲线法检测HER2基因的多态性。
在本报告中,我们采用基于实时温度熔解(Tm)位移SYBR Green I的熔解曲线法进行等位基因鉴别。分析了扩增的DNA HER-2 Ile655Val的熔解曲线及其特征。
HER2基因GG和AA等位基因的Tm值分别为85±0.14°C和82.5±0.23°C,而GG、AG和AA等位基因的循环阈值(Ct)值分别为19.6±0.27、22.5±0.23、18.6±0.22;此外,无模板对照显示Ct值为31.18±0.27。所开发方法的特征为在62°C时最佳退火,kappa系数值为1,平均值与PCR测序几乎一致。GG、AG和AA的批内变异系数在0.2%-1%范围内,而各批次间的变异系数在0.7%-1%范围内。此外,基于PCR的保质期检测显示在储存观察3个月内具有稳定性。
这种方法可被认为是简单、快速且低成本的,有助于HER2流行病学的快速研究。此外,所开发的方法可能有助于临床医生处理乳腺癌患者,特别是在考虑曲妥珠单抗的心脏毒性作用方面。