Huang Chi-Cheng, Lin Min-Rou, Yang Yu-Chen, Hsu Yu-Wen, Wong Henry Sung-Ching, Chang Wei-Chiao
Comprehensive Breast Health Center, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
College of Medicine, Taipei Medical University, Taipei 11031, Taiwan.
J Pers Med. 2020 Dec 17;10(4):287. doi: 10.3390/jpm10040287.
Among all cancers in women, breast cancer has the highest incidence. The mortality of breast cancer is highly associated with metastasis. Migration and malignant transformation of cancer cells have been reported to be modulated by store-operated calcium (SOC) channels, which control calcium signaling and cell proliferation pathways. Stromal interaction molecule 1 ( is a calcium sensor in the endoplasmic reticulum, triggering the activation of store-operated calcium signaling. However, the clinical relevance of in breast cancer is still unclear. Here, we recruited 348 breast cancer patients and conducted a genetic association study to address this question. Four tagging germline single nucleotide variants (SNVs) in were selected and RNA sequencing data of 525 breast cancer samples from The Cancer Genome Atlas (TCGA) database were evaluated. The results show that rs2304891 and rs3750996 were correlated with clinical stage of breast cancer. Expression quantitative trait loci (eQTL) analysis indicated that risk G allele of contributed to the higher expression of . In addition, we found an increased risk of rs2304891 G allele and rs3750996 A allele in estrogen receptor (ER) positive and progesterone receptor (PR) positive patients. In conclusion, our results suggest that germline SNV, rs2304891 and rs3750996 as well as expression are important biomarkers for the prediction of clinical outcomes in breast cancer patients.
在女性的所有癌症中,乳腺癌的发病率最高。乳腺癌的死亡率与转移高度相关。据报道,癌细胞的迁移和恶性转化受储存性钙(SOC)通道调节,该通道控制钙信号传导和细胞增殖途径。基质相互作用分子1(STIM1)是内质网中的一种钙传感器,可触发储存性钙信号传导的激活。然而,STIM1在乳腺癌中的临床相关性仍不清楚。在此,我们招募了348名乳腺癌患者并进行了一项基因关联研究以解决这个问题。我们选择了STIM1基因中的四个标签种系单核苷酸变异(SNV),并评估了来自癌症基因组图谱(TCGA)数据库的525份乳腺癌样本的RNA测序数据。结果表明,rs2304891和rs3750996与乳腺癌的临床分期相关。表达数量性状位点(eQTL)分析表明,STIM1的风险G等位基因导致了其更高的表达。此外,我们发现雌激素受体(ER)阳性和孕激素受体(PR)阳性患者中rs2304891 G等位基因和rs3750996 A等位基因的风险增加。总之,我们的结果表明种系SNV、rs2304891和rs3750996以及STIM1表达是预测乳腺癌患者临床结局的重要生物标志物。