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骨桥蛋白和血小板反应蛋白-1在促进原发性切除非小细胞肺癌的肿瘤侵袭性方面发挥相反作用。

Osteopontin and thrombospondin-1 play opposite roles in promoting tumor aggressiveness of primary resected non-small cell lung cancer.

作者信息

Rouanne Mathieu, Adam Julien, Goubar Aïcha, Robin Angélique, Ohana Caroline, Louvet Emilie, Cormier Jiemin, Mercier Olaf, Dorfmüller Peter, Fattal Soly, de Montpreville Vincent Thomas, Lebret Thierry, Dartevelle Philippe, Fadel Elie, Besse Benjamin, Olaussen Ken André, Auclair Christian, Soria Jean-Charles

机构信息

INSERM Unit U981, Gustave Roussy Cancer Campus, 114, rue Edouard Vaillant, 94805, Villejuif, France.

Université Paris Sud, Université Paris-Saclay, 94270, Le Kremlin-Bicêtre, France.

出版信息

BMC Cancer. 2016 Jul 15;16:483. doi: 10.1186/s12885-016-2541-5.

Abstract

BACKGROUND

Osteopontin (OPN) and thrombospondin-1 (TSP-1) are extracellular matrix proteins secreted by stromal and tumor cells. These proteins appear to have a key role in the tumor microenvironment for cancer development and metastasis. There is little information regarding the prognostic value of the combination of these two proteins in human cancers. Our aim was to clarify clinical significance and prognostic value of each circulating protein and their combination in primary resected non-small cell lung cancer (NSCLC) patients.

METHODS

We retrospectively reviewed 171 patients with NSCLC following curative intent surgery from January to December of 2012. Preoperative serums, demographics, clinical and pathological data and molecular profiling were analyzed. Pre-treatment OPN and TSP-1 serum levels were measured by ELISA. Tissue protein expression in primary tumor samples was determined by immunohistochemical analysis.

RESULTS

OPN and TSP-1 serum levels were inversely correlated with survival rates. For each 50 units increment of serum OPN, an increased risk of metastasis by 69 % (unadjusted HR 1.69, 95 % CI 1.12-2.56, p = 0.01) and an increased risk of death by 95 % (unadjusted HR 1.95, 95 % CI 1.15-3.32, p = 0.01) were observed. Conversely, for each 10 units increment in TSP-1, the risk of death was decreased by 85 % (unadjusted HR 0.15, 95 % CI 0.03-0.89; p = 0.04). No statistically significant correlation was found between TSP-1 serum level and distant metastasis-free survival (p = 0.2). On multivariate analysis, OPN and TSP-1 serum levels were independent prognostic factors of overall survival (HR 1.71, 95 % CI 1.04-2.82, p = 0.04 for an increase of 50 ng/mL in OPN; HR 0.18, 95 % CI 0.04-0.87, p = 0.03 for an increase of 10 ng/mL in TSP-1). In addition, the combination of OPN and TSP-1 serum levels remained an independent prognostic factor for overall survival (HR 1.31, 95 % CI 1.03-1.67, p = 0.03 for an increase of 6 ng/mL in OPN/TSP-1 ratio).

CONCLUSIONS

Our results show that pre-treatment OPN and TSP-1 serum levels may reflect the aggressiveness of the tumor and might serve as prognostic markers in patients with primary resected NSCLC.

摘要

背景

骨桥蛋白(OPN)和血小板反应蛋白-1(TSP-1)是由基质细胞和肿瘤细胞分泌的细胞外基质蛋白。这些蛋白似乎在肿瘤微环境中对癌症的发展和转移起关键作用。关于这两种蛋白联合检测在人类癌症中的预后价值,目前所知甚少。我们的目的是阐明每种循环蛋白及其联合检测在原发性非小细胞肺癌(NSCLC)患者中的临床意义和预后价值。

方法

我们回顾性分析了2012年1月至12月间171例行根治性手术的NSCLC患者。分析术前血清、人口统计学、临床和病理数据以及分子特征。采用酶联免疫吸附测定(ELISA)法检测术前血清OPN和TSP-1水平。通过免疫组化分析确定原发性肿瘤样本中的组织蛋白表达。

结果

OPN和TSP-1血清水平与生存率呈负相关。血清OPN每增加50个单位,转移风险增加69%(未校正风险比[HR]1.69,95%置信区间[CI]1.12 - 2.56,p = 0.01),死亡风险增加95%(未校正HR 1.95,95% CI 1.15 - 3.32,p = 0.01)。相反,TSP-1每增加10个单位,死亡风险降低85%(未校正HR 0.15,95% CI 0.03 - 0.89;p = 0.04)。未发现TSP-1血清水平与无远处转移生存期之间存在统计学显著相关性(p = 0.2)。多因素分析显示,OPN和TSP-1血清水平是总生存期的独立预后因素(OPN每增加50 ng/mL,HR 1.71,95% CI 1.04 - 2.82,p = 0.04;TSP-1每增加10 ng/mL,HR 0.18,95% CI 0.04 - 0.87,p = 0.03)。此外,OPN和TSP-1血清水平联合检测仍是总生存期的独立预后因素(OPN/TSP-1比值每增加6 ng/mL,HR 1.31,95% CI 1.03 - 1.67,p = 0.03)。

结论

我们的结果表明,术前OPN和TSP-1血清水平可能反映肿瘤的侵袭性,并可能作为原发性NSCLC患者的预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1766/4947364/9eb83fadfddc/12885_2016_2541_Fig1_HTML.jpg

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