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Trefoil factor-3 expression in human colon cancer liver metastasis

机译:三叶因子-3在人结肠癌肝转移中的表达

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Deaths from colorectal cancer are often due to liver metastasis. Trefoil factor-3 (TFF3) is expressed by normal intestinal epithelial cells and its expression is maintained throughout the colon adenoma-carcinoma sequence. Our previous work demonstrated a correlation between TFF3 expression and metastatic potential in an animal model of colon cancer. The aim of this study was to determine whether TFF3 is expressed in human colon cancer liver metastasis (CCLM) and whether inhibiting TFF3 expression in colon cancer cells would alter their invasive potential in vitro. Human CCLMs were analyzed at the mRNA and protein level for TFF3 expression. Two highly metastatic rat colon cancer cell lines that either natively express TFF3 (LN cells) or were transfected with TFF3 (LPCRI-2 cells), were treated with two rat TFF3 siRNA constructs (si78 and si365), and analyzed in an in vitro invasion assay. At the mRNA and protein level, TFF3 was expressed in 17/17 (100%) CCLMs and 10/11 (91%) primary colon cancers, but not in normal liver tissue. By real time PCR, TFF3 expression was markedly inhibited by both siRNA constructs in LN and LPCRI-2 cells. The si365 and si78 constructs inhibited invasion by 44% and 53%, respectively, in LN cells, and by 74% and 50%, respectively, in LPCRI-2 cells. These results provide further evidence that TFF3 contributes to the malignant behavior of colon cancer cells. These observations may have relevance for designing new diagnostic and treatment approaches to colorectal cancer.
机译:大肠癌的死亡通常归因于肝转移。三叶因子3(TFF3)由正常肠上皮细胞表达,并且其表达在整个结肠腺瘤-癌序列中均得到维持。我们先前的工作证明了结肠癌动物模型中TFF3表达与转移潜能之间的相关性。这项研究的目的是确定TFF3是否在人类结肠癌肝转移(CCLM)中表达,以及抑制TFF3在结肠癌细胞中的表达是否会改变其体外侵袭潜能。在mRNA和蛋白水平上分析了人CCLM的TFF3表达。用两种大鼠TFF3 siRNA构建体(si78和si365)处理两种天然表达TFF3(LN细胞)或用TFF3(LPCRI-2细胞)转染的高转移大鼠结肠癌细胞系,并在体外侵袭中进行分析分析。在mRNA和蛋白质水平上,TFF3在17/17(100%)CCLM和10/11(91%)原发性结肠癌中表达,但在正常肝组织中不表达。通过实时PCR,在LN和LPCRI-2细胞中,两种siRNA构建体均显着抑制了TFF3的表达。 si365和si78构建体在LN细胞中分别抑制了44%和53%的侵袭,在LPCRI-2细胞中分别抑制了74%和50%的侵袭。这些结果提供了进一步的证据,表明TFF3有助于结肠癌细胞的恶性行为。这些观察结果可能与设计大肠癌的新诊断和治疗方法有关。

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