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Coiled-coil domain-containing protein 8 inhibits the invasiveness and migration of non small cell Lung cancer cells

机译:含有卷线圈结构域的蛋白质8抑制非小细胞肺癌细胞的侵袭性和迁移

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摘要

Lung cancer has always been the leading cause of death among patients with malignant tumors, and the majority of these patients die because of cancer cell invasion and metastasis. Previous studies have implicated coiled-coil domain-containing protein 8 (CCDC8) as a tumor suppressor in several types of cancer, such as breast and prostate cancers. However, the expression levels or functions of CCDC8 in lung cancer have not been elucidated. Here, we used immunohistochemical staining to measure CCDC8 expression in 147 samples from tumors and 30 samples from the adjacent normal lung tissues of patients with non small cell lung cancer. CCDC8 was shown to be located predominantly in the cytoplasm and partially on the cell membrane, and its expression level was significantly lower in lung cancer samples than that in the adjacent normal lung tissues (P = .001). CCDC8 expression was closely related to tumor differentiation (P = .039), tumor-node-metastasis stage (P = .009), lymph node metastasis (P = .038), and prognosis (P = .043) of lung cancer. Transfection of A549 cells with CCDC8 significantly reduced cell invasion and migration (P < .05), whereas the invasiveness and migration capacity in CCDC8-knockdown A549 cells were significantly increased in comparison with the control cells (P < .05). Furthermore, we demonstrated that CCDC8 can downregulate the expression of Snail and upregulate the expression of E-cadherin by inhibiting p-P38 and p-I kappa B alpha. Collectively, CCDC8 may suppress the invasion and metastasis of lung cancer cells, and it may represent a promising therapeutic target for non-small cell lung cancer. (C) 2016 Elsevier Inc. All rights reserved.
机译:肺癌始终是恶性肿瘤患者死亡的主要原因,由于癌细胞侵袭和转移,这些患者的大多数死亡。以前的研究将含有卷曲卷域域的蛋白质8(CCDC8)含有若干类型癌症的肿瘤抑制剂,例如乳腺癌和前列腺癌。然而,肺癌中CCDC8的表达水平或功能尚未阐明。在这里,我们使用免疫组化染色来测量来自肿瘤的147个样品中的CCDC8表达和来自非小细胞肺癌患者的相邻正常肺组织的30个样品。显示CCDC8主要位于细胞质中,部分在细胞膜上位于细胞膜上,并且其表达水平在肺癌样品中显着降低,而不是相邻的正常肺组织(P = .001)。 CCDC8表达与肿瘤分化(p = .039),肿瘤节点转移阶段(p = .009),淋巴结转移(p = .038),肺癌预后(p = .043)。用CCDC8转染A549细胞显着降低细胞侵袭和迁移(P <.05),而CCDC8-kextickdown A549细胞中的侵袭性和迁移容量与对照细胞相比显着增加(P <.05)。此外,我们证明CCDC8可以下调蜗牛的表达并通过抑制p-p38和p-1κBα来上调E-cadherin的表达。 CCDC8集体可以抑制肺癌细胞的侵袭和转移,并且它可能代表非小细胞肺癌的有希望的治疗靶标。 (c)2016年Elsevier Inc.保留所有权利。

著录项

  • 来源
    《Human Pathology》 |2016年第2016期|共10页
  • 作者单位

    China Med Univ Dept Pathol Affiliated Hosp 1 Shenyang 110001 Peoples R China;

    China Med Univ Dept Pathol Affiliated Hosp 1 Shenyang 110001 Peoples R China;

    China Med Univ Canc Hosp Dept Pathol Shenyang 110042 Peoples R China;

    China Med Univ Dept Pathol Affiliated Hosp 1 Shenyang 110001 Peoples R China;

    China Med Univ Dept Pathol Affiliated Hosp 1 Shenyang 110001 Peoples R China;

    China Med Univ Dept Pathol Affiliated Hosp 1 Shenyang 110001 Peoples R China;

    China Med Univ Dept Pathol Affiliated Hosp 1 Shenyang 110001 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 病理学;
  • 关键词

    CCDC8; NSCLC; Invasion; Migration; EMT;

    机译:CCDC8;NSCLC;入侵;迁移;EMT;

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