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首页> 外文期刊>Cancer Cell International >Basigin-2 upregulated by receptor activator of NF-κB ligand enhances lung cancer-induced osteolytic lesions
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Basigin-2 upregulated by receptor activator of NF-κB ligand enhances lung cancer-induced osteolytic lesions

机译:Basigin-2被NF-κB受体激活剂上调可增强肺癌引起的溶骨性病变

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Background Lung cancer bone metastasis causes poor prognosis. Basigin-2, a novel cancer-associated biomarker, is upregulated in lung cancer and has been linked with tumor progression. But little is known about the role of basigin-2 in lung cancer bone metastasis and osteolytic lesion. Methods Basigin-2 expression was evaluated in biopsy tissue specimens of 20 lung cancer patients with bone metastases via immunohistochemistry. Invasion assay and MTT proliferation assay were performed to test the invasion and proliferation of lung cancer cell after modulated basigin-2 expression. The osteoclastic activity of basigin-2 was detected in tibia cancer model by injected of lung cancer cells. The regulation role of receptor activator of NF-κB ligand (RANKL) on basigin-2 and its downstream molecules were measured by real-time quantitative RT-PCR, gelatin zymography and western blot analysis. Results We found that basigin-2 was highly expressed in lung cancer bone metastases. Then, we demonstrated that basigin-2 could promote lung cancer cells invasion, metastasis and proliferation through upregulating metalloproteinases-2 (MMP-2), MMP-9 and vascular endothelial growth factor (VEGF) expression. The lung cancer cells overexpressing basigin-2 strongly induced the osteolytic lesions in immunodeficient mice, which were reduced by treatment with basigin-2 blocking antibody. Furthermore, we explored the enhanced basigin-2 molecular mechanism in lung cancer bone metastasis. Our results indicated the RANKL, pivotal for the control of bone resorption, could increase basigin-2 and its downstream molecules MMP-2, MMP-9 and VEGF expression in vitro. Conclusions Basigin-2 upregulated by RANKL induces MMPs and VEGF, which may increase lung cancer cell metastasis ability and support osteoclastic activity. Thus, our data suggest important roles for basigin-2 in lung cancer-induced osteolytic lesion and implicate this protein potential application as a target for lung cancer bone metastasis therapy.
机译:背景肺癌骨转移导致不良预后。 Basigin-2是一种新型的癌症相关生物标志物,在肺癌中被上调,并与肿瘤的进展有关。但是,关于basigin-2在肺癌骨转移和溶骨性病变中的作用知之甚少。方法采用免疫组织化学方法检测20例肺癌骨转移患者活检组织中Basigin-2的表达。进行侵袭测定和MTT增殖测定以测试调节的basigin-2表达后肺癌细胞的侵袭和增殖。通过注入肺癌细胞,在胫骨癌模型中检测到basigin-2的破骨活性。通过实时定量RT-PCR,明胶酶谱分析和western blot分析来测定NF-κB配体受体激活剂(RANKL)对basigin-2及其下游分子的调控作用。结果我们发现basigin-2在肺癌骨转移中高表达。然后,我们证明了basigin-2可以通过上调金属蛋白酶2(MMP-2),MMP-9和血管内皮生长因子(VEGF)的表达来促进肺癌细胞的侵袭,转移和增殖。过度表达basigin-2的肺癌细胞在免疫缺陷小鼠中强烈诱导溶骨性病变,通过使用basigin-2封闭抗体治疗可减轻这种溶骨性病变。此外,我们探讨了增强的basigin-2分子机制在肺癌骨转移中的作用。我们的结果表明,RANKL是控制骨吸收的关键,在体外可以增加basigin-2及其下游分子MMP-2,MMP-9和VEGF的表达。结论RANKL上调Basigin-2诱导MMPs和VEGF的表达,可能增强肺癌细胞的转移能力,并支持破骨细胞活性。因此,我们的数据表明basigin-2在肺癌诱导的溶骨性病变中起重要作用,并暗示该蛋白潜在的应用作为肺癌骨转移治疗的靶标。

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