小脯氨酸富蛋白1A促进肺腺癌的进展并预示不利的临床结果。

Shenqiu Wang, Wenmei Zhang
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引用次数: 2

摘要

小脯氨酸富蛋白1A (Small Proline Rich Protein 1A, SPRR1A)在调节鳞状细胞分化中起关键作用。有报道称SPRR1A过表达与胃癌、结肠癌等肿瘤的进展密切相关。然而,SPRR1A在肺腺癌(LUAD)中的功能尚未阐明。我们首先检测了SPRR1A在LUAD组织中的表达模式,结果表明,与正常肺组织相比,SPRR1A在LUAD组织中的表达水平显著升高。SPRR1A的高表达与肿瘤大小密切相关。SPRR1A表达较高的LUAD患者总生存期较差,SPRR1A被认为是一个独立的不良预后因素。此外,通过细胞实验检测SPRR1A对肺癌细胞的作用,结果表明,敲低SPRR1A可以抑制肿瘤细胞的增殖和侵袭能力,而过表达SPRR1A则相反。最后,我们的研究结果得到了小鼠体内异种移植物模型数据的证实。综上所述,SPRR1A表达较高的LUAD患者更容易出现较差的临床结局和不良预后,提示SPRR1A作为一种新的临床生物标志物和治疗靶点的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Small Proline Rich Protein 1A promotes lung adenocarcinoma progression and indicates unfavorable clinical outcomes.
Small Proline Rich Protein 1A (SPRR1A) plays a critical role in regulating squamous cell differentiation. It has been reported that SPRR1A overexpression was closely related to the progression of some tumors such as gastric cancer and colon cancer. However, the function of SPRR1A in lung adenocarcinoma (LUAD) has not been elucidated. Here we firstly examined the expression pattern of SPRR1A in LUAD tissues, which indicated that SPRR1A expression level was significantly elevated in LUAD tissues compared to normal lung tissues. High expression of SPRR1A was closely related to the larger tumor size. LUAD patients with higher SPRR1A expression had poorer overall survival and SPRR1A was identified as an independent unfavorable prognosis factor. In addition, the effects of SPRR1A on lung cancer cells were tested through cellular experiments and the result demonstrated that knockdown of SPRR1A can suppress proliferation and invasion capacities of tumor cells, while overexpressing SPRR1A exerted opposite effects. Finally, our findings were substantiated by the data obtained from in vivo xenografts using mice model. In conclusion, LUAD patients with higher SPRR1A expression were more predisposed to poorer clinical outcomes and unfavorable prognosis, indicating the potential role of SPRR1A as a novel clinical biomarker and therapeutic target.
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