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首页> 外文期刊>Journal of Physics: Conference Series >Expression profile of stem cell pathway genes in patients with advanced breast cancer after neoadjuvant therapy
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Expression profile of stem cell pathway genes in patients with advanced breast cancer after neoadjuvant therapy

机译:新辅助治疗后晚期乳腺癌患者干细胞通路基因的表达谱

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Presence of breast cancer stem cells (BCSCs) is one of reasons for therapy resistance and metastatic development. Currently, neoadjuvant therapy is widely applied for local advanced breast cancer prior to tumor resection. This study aimed to analyze existence of BCSCs after neoadjuvant therapy and determine their correlation with clinical characteristics and patient survival. Cancer tissues were collected from 46 patients with stage IIIb or IV breast cancer before and after chemotherapy or hormone neoadjuvant therapy. The expression profiles of stem cell pathway genes were then investigated using next generation sequencing (Miseq, Illumina) and TruSeq Targeted RNA Expression stem cell panel kit (Illumina) comprising 100 genes. Altered stem cell gene expression was analyzed using paired t-test and correlated with clinical characteristics. Twelve stem cell pathway genes were significantly altered after neoadjuvant therapy, comprising six upregulated genes (ALDH1A1, ALDH2, CCND2, CXCL12, FZD7, and IGF1) and six downregulated genes (CCNE1, CDC42, CTNNB1, HDAC2, PSEN1, and PSENEN). We observed a significant increase in ALDH1A1 in the 3-year non-survival group and a poor survival rate of patients in high CDC42 and HDAC2 expression group. It can be concluded that overexpression of ALDH1A1, CDC42, and HDAC2 after neoadjuvant chemotherapy is correlated with poor prognosis in advanced breast cancer.
机译:乳腺癌干细胞(BCSCs)的存在是治疗抗性和转移发展的原因之一。目前,新辅助疗法已广泛应用于肿瘤切除之前的局部晚期乳腺癌。这项研究旨在分析新辅助治疗后BCSC的存在,并确定其与临床特征和患者生存率的相关性。在化疗或激素新辅助治疗前后,从46例IIIb或IV期乳腺癌患者中收集了癌组织。然后使用下一代测序(Miseq,Illumina)和包含100个基因的TruSeq靶向RNA表达干细胞检测试剂盒(Illumina)研究干细胞途径基因的表达谱。干细胞基因表达的改变使用配对t检验进行分析,并与临床特征相关。新辅助治疗后,十二个干细胞途径基因发生了显着改变,包括六个上调基因(ALDH1A1,ALDH2,CCND2,CXCL12,FZD7和IGF1)和六个下调基因(CCNE1,CDC42,CTNNB1,HDAC2,PSEN1和PSENEN)。我们观察到在3年非存活组中ALDH1A1显着增加,而高CDC42和HDAC2表达组中患者的存活率较差。可以得出结论,新辅助化疗后ALDH1A1,CDC42和HDAC2的过表达与晚期乳腺癌的不良预后相关。

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