2014
DOI: 10.3892/br.2014.319
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Clinical significance of serum and tumor tissue endostatin evaluation in operable non-small cell lung cancer

Abstract: Abstract. Endostatin, as the most potential antiangiogenic factor, is a naturally occurring fragment of collagen XVIII in bloodstream capable of inhibiting tumor growth and metastasis. This study was conducted to explore the clinical value of endostatin in serum and tumor tissue in patients with operable non-small cell lung cancer (NSCLC). ELISA and immunohistochemistry were applied to detect the expression of endostatin in serum and tumor tissue in 105 patient-matched operable NSCLC patients. The serum level … Show more

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Cited by 5 publications
(2 citation statements)
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“…Recombinant endostatin has been considered as a broad-spectrum anticancer agent because of its endogenous inhibitory effect on angiogenesis, non-toxicity, and synergistic ability with chemotherapy drugs ( Boehm et al, 1997 ; Folkman, 2006 ; Zhuang and Yuan, 2009 ). Currently, recombinant endostatin (Endostar) has been approved for the treatment of NSCLC by the State Food and Drug Administration of China, which is expressed and purified in E. coli with an additional nine-amino acid sequence ( Hu et al, 2014 ). However, its short half-life and instability limit clinical applications.…”
Section: Discussionmentioning
confidence: 99%
“…Recombinant endostatin has been considered as a broad-spectrum anticancer agent because of its endogenous inhibitory effect on angiogenesis, non-toxicity, and synergistic ability with chemotherapy drugs ( Boehm et al, 1997 ; Folkman, 2006 ; Zhuang and Yuan, 2009 ). Currently, recombinant endostatin (Endostar) has been approved for the treatment of NSCLC by the State Food and Drug Administration of China, which is expressed and purified in E. coli with an additional nine-amino acid sequence ( Hu et al, 2014 ). However, its short half-life and instability limit clinical applications.…”
Section: Discussionmentioning
confidence: 99%
“…Here, we showed that GSTA1 mRNA expression was down-regulated in HCCs with respect to non-tumor tissues. Importantly, low GSTA1 expression in HCCs was proportional to high tumor size and low expression of the liver-enriched genes albumin [36] and procollagen type XVIII [37]. In addition, GSTA1 expression, in an independent set of 247 HCCs, was associated with the expression of liver-enriched genes, such as HNF4A, MAT1A, SDS, ARG1 as well as of several members of the cytochrome P450 family involved in well-differentiated hepatocyte-specific metabolic functions.…”
Section: Discussionmentioning
confidence: 99%