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Silencing SATB1 with siRNA inhibits the proliferation and invasion of small cell lung cancer cells

DOI: 10.1186/1475-2867-13-8

Keywords: SATB1, Small cell lung cancer, siRNA interfering, Apoptosis

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Abstract:

The level of SATB1 was analyzed in SCLC tissues, metastatic lymphoid nodes and adjacent normal lung tissues by immunohistochemistry. Meanwhile, small interfering SATB1-targeting RNA was constructed and transfected into human SCLC cell line NCI-H446 to evaluate the effects of SATB1-siRNA on cell proliferation, invasion and apoptosis.SATB1 protein was overexpressed in SCLC tissues and metastasis lymphoid nodes compared with adjacent normal lung tissues. Compared with control group, SATB1-siRNA inhibits the proliferation and invasion of SCLC cells and induces SCLC cells apoptosis statistically (P<0.05) in vitro.Our results suggest that SATB1 plays an important role in the metastasis of human SCLC cell.Small cell lung cancer (SCLC) is a special kind of lung cancer, which comprises 15%-20% of all lung cancers. Different from other lung cancers, SCLC exhibits aggressive behavior with rapid growth and spread to distant sites early [1]. Although SCLC is exquisite sensitivity to chemotherapy and radiation, it is more prone to relapse and recurrence. Special AT-rich sequence binding protein 1 (SATB1) is a nuclear matrix attachment region binding protein (MBP) which participates in higher-order chromatin organization and tissue-specific gene expression [2,3]. SATB1 play an important role in differentiation, and expresses at high level in thymocyte, its expression is down-regulated in mature T cells [4,5]. SATB1 has been reported to promote a metastatic phenotype and correlate with poor prognosis in breast cancer [6]. Its expression has also been associated with unfavourable clinicopathological characteristics and poor prognosis in gastric, liver and colorectal cancer and glioma [7-12]. RNA-interference-mediated knockdown in aggressive cancer cells have altered the expression of over 1,000 genes, this technique effectively inhibited cell capacity of proliferation, invasion, tumor growth and metastasis [6]. Zheng et al. also found SATB1 expression in aggressive rather than non-a

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