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OPN-a splicing variant expression in non-small cell lung cancer and its effects on the bone metastatic abilities of lung cancer cells in vitro

机译:非小细胞肺癌中OPN-a剪接变体表达及其对肺癌骨转移能力的影响

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摘要

Background: Osteopontin (OPN) is known to be involved in the development of certain cancers, including non-small cell lung cancer (NSCLC). However, its role in tumour progression remains unclear. The present study investigated the expression and biological impact of the OPN variant, OPN-a in NSCLC. Materials and Methods: OPN-a splicing variant expression in human NSCLC tissues was analyzed by real-time qPCR and immunohistochemistry (IHC), respectively. The impact of OPN-a on cellular functions of lung cancer cells was also evaluated. In addition, an in vitro model was developed for the assessment of interactions between lung cancer cells and bone tissue. Results: The expression of OPN-a was higher in lung cancer tissues compared to normal controls. OPN-a promoted the malignant phenotypes of A549 cells by enhancing cell-adherent abilities to bone tissues, which could be mediated by the interaction with the cell surface receptor αvβ3 integrin. Conclusion: OPN-a may represent a bone metastatic factor in human lung cancer, as well as a potential therapy target.
机译:背景:骨桥蛋白(OPN)参与某些癌症的发展,包括非小细胞肺癌(NSCLC)。然而,其在肿瘤进展中的作用仍不清楚。本研究调查了OPN变体OPN-a在NSCLC中的表达及其生物学影响。材料和方法:分别通过实时定量PCR和免疫组化(IHC)分析人非小细胞肺癌组织中OPN-a剪接变体的表达。还评估了OPN-a对肺癌细胞功能的影响。另外,开发了用于评估肺癌细胞与骨组织之间相互作用的体外模型。结果:与正常对照组相比,肺癌组织中OPN-a的表达更高。 OPN-a通过增强细胞对骨组织的粘附能力来促进A549细胞的恶性表型,这可以通过与细胞表面受体αvβ3整联蛋白的相互作用来介导。结论:OPN-a可能代表人肺癌的骨转移因子,也是潜在的治疗靶点。

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