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化疗可有效抑制肺腺癌伴骨转移患者体内白细胞介素-20、核因子κB受体激活剂配体及骨保护素水平。

Chemotherapy effectively suppresses interleukin-20, receptor activator of nuclear factor kappa-B ligand, and osteoprotegerin levels in patients with lung adenocarcinoma and bone metastasis.

作者信息

Yu Mingyang, Su Yun, Cui Daping, Sun Qiang, Luan Bowu, Zhao Dewei

机构信息

Department of Traumatic Orthopedics, Affiliated Zhongshan Hospital of Dalian University, Dalian, Liaoning, China.

Department Chemistry, Stony Brook University, NY, USA.

出版信息

J Cancer Res Ther. 2016 Apr-Jun;12(2):963-8. doi: 10.4103/0973-1482.179085.

DOI:10.4103/0973-1482.179085
PMID:27461682
Abstract

BACKGROUND

Bone metastasis (BM) is common in patients with lung cancer. Osteolysis is caused by increased osteoclast activity. Interleukin-20 (IL-20) and receptor activator of nuclear factor kappa-B ligand (RANKL) are crucial for osteoclast formation. Osteoprotegerin (OPG) inhibits a receptor activator of RANKL/RANK signaling. The aims of this study were to analyze the serum levels of IL-20, OPG, and RANKL in patients with and without BM and to observe the effect of chemotherapy on these cytokines.

PATIENTS AND METHODS

A total 54 cases of pathologically confirmed lung adenocarcinoma (ADC) and 18 healthy individuals (Control) were enrolled in this study. Eligible patients were divided into three groups (18 patients per group): ADC without BM (ADC), ADC with BM (ADC + BM), and ADC with BM treated with chemotherapy (ADC + BM + Chemo). Serum IL-20, RANKL, and OPG levels were analyzed by enzyme-linked immunosorbent assay.

RESULTS

Serum IL-20, RANKL, and OPG levels in ADC + BM patients were significantly elevated compared with that in the Control or ADC groups (both P < 0.001). The serum cytokine levels were significantly lower following chemotherapy compared with that in patients who did not receive chemotherapy (P < 0.001).

CONCLUSIONS

Serum IL-20, RANKL, and OPG levels increase in patients with lung cancer and BMs. Chemotherapy suppresses the elevation of these cytokines.

摘要

背景

骨转移(BM)在肺癌患者中很常见。骨溶解是由破骨细胞活性增加引起的。白细胞介素-20(IL-20)和核因子κB受体活化因子配体(RANKL)对破骨细胞形成至关重要。骨保护素(OPG)抑制RANKL/RANK信号的受体活化因子。本研究的目的是分析有无骨转移的肺癌患者血清中IL-20、OPG和RANKL水平,并观察化疗对这些细胞因子的影响。

患者与方法

本研究纳入54例经病理确诊的肺腺癌(ADC)患者和18名健康个体(对照组)。符合条件的患者分为三组(每组18例):无骨转移的肺腺癌(ADC)组、有骨转移的肺腺癌(ADC + BM)组和接受化疗的有骨转移的肺腺癌(ADC + BM + Chemo)组。采用酶联免疫吸附测定法分析血清IL-20、RANKL和OPG水平。

结果

与对照组或ADC组相比,ADC + BM组患者血清IL-20、RANKL和OPG水平显著升高(均P < 0.001)。与未接受化疗的患者相比,化疗后血清细胞因子水平显著降低(P < 0.001)。

结论

肺癌合并骨转移患者血清IL-20、RANKL和OPG水平升高。化疗可抑制这些细胞因子的升高。

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