血清NK细胞活化性受体、γ干扰素与非小细胞肺癌患者病情程度、预后的相关性分析
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作者单位:

沧州市中心医院 胸外科, 河北 沧州 061000

通讯作者:

宋翔,E-mail:xiangsvit@163.com

中图分类号:

R734.2

基金项目:

河北省2021年度医学科学研究课题计划(No:20211362)


Correlation analysis of serum NKG2D and IFN-γ levels with disease severity and prognosis of patients with non-small cell lung cancer
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Affiliation:

Department of Thoracic Surgery, Cangzhou Central Hospital, Cangzhou, Hebei 061000, China

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    摘要:

    目的 分析血清NK细胞活化性受体(NKG2D)、γ干扰素(IFN-γ)与非小细胞肺癌(NSCLC)患者病情程度、预后的相关性。方法 选取沧州市中心医院2020年5月—2021年5月收治的NSCLC患者150例为研究对象,根据TNM分期标准分为Ⅰ、Ⅱ期组50例和Ⅲ、Ⅳ期组100例。比较两组患者的血清NKG2D、IFN-γ、肿瘤标志物[癌胚抗原(CEA)、细胞角质蛋白19片段抗原21-1(CYFRA21-1)、糖类抗原125(CA125)]及6个月内病死率;采用Pearson法检验血清NKG2D、IFN-γ与肿瘤标志物的相关性;比较不同预后NSCLC患者血清NKG2D、IFN-γ;绘制ROC曲线,分析血清NKG2D、IFN-γ及两者联合预测NSCLC患者预后的价值。结果 Ⅲ、Ⅳ期组血清NKG2D[(67.12±5.28)%]低于Ⅰ、Ⅱ期组[(81.50±7.33)%](P <0.05),血清IFN-γ[(23.67±5.74)ng/mL]、CEA[(43.76±6.48)ng/mL]、CA125[(35.62±6.03)u/mL]、CYFRA21-1[(11.69±1.86)ng/mL]高于Ⅰ、Ⅱ期组[(17.91±4.82)ng/mL、(21.53±4.62)ng/mL、(23.59±5.17)u/mL、(6.84±1.12)ng/mL](P <0.05)。Pearson相关性分析显示,血清NKG2D与CEA(r =-0.683)、CA125(r =-0.615)、CYFRA21-1(r =-0.704)均呈负相关(P <0.05);IFN-γ与CEA(r =0.512)、CA125(r =0.439)、CYFRA21-1(r =0.543)均呈正相关(P <0.05)。150例NSCLC患者病死率为22.67%(34/150)。Ⅲ、Ⅳ期组6个月内病死率为28.00%(28/100),Ⅰ、Ⅱ期组6个月内病死率为12.00%(6/50),经χ2检验,差异有统计学意义(χ2 =4.868,P =0.027)。死亡组血清NKG2D[(58.58±5.62)%]低于非死亡组[(84.23±4.39)%](P <0.05),血清IFN-γ[(29.93±3.17)ng/mL]高于非死亡组[(20.95±2.20)ng/mL](P <0.05)。ROC曲线显示,IFN-γ、NKG2D及两者联合预测NSCLC患者预后的AUC分别为0.780(95% CI:0.673,0.942)、0.820(95% CI:0.675,0.955)、0.860(95% CI:0.761,0.984),敏感性分别为78.1%(95% CI:0.648,0.892)、82.6%(95% CI:0.713,0.955)、86.5%(95% CI:0.752,0.978),特异性为51.3%(95% CI:0.443,0.714)、53.6%(95% CI:0.467,0.735)、41.5%(95% CI:0.328,0.616)。结论 血清NKG2D、IFN-γ与NSCLC患者病情程度、肿瘤标志物水平有关,且两者联合检测可有效预测患者早期预后。

    Abstract:

    Objective To analyze the correlation of serum NK cell activation receptor (NKG2D) and IFN-γ (IFN-γ) levels with the severity and prognosis of non-small cell lung carcinoma (NSCLC) patients.Methods A total of 150 NSCLC patients admitted to Cangzhou Central Hospital from May 2020 to May 2021 were selected as research subjects and divided into group I/Ⅱ (50 cases) and group Ⅲ/Ⅳ (100 cases) according to TNM staging criteria. The two groups of serum NKG2D, IFN-γ, tumor markers [carcinoembryonic antigen (CEA), human cytokeratin 21-1 fragment (CYFRA21-1), sugar antigen 125 (CA125)], and 6-month survival rate were recorded. Bivariate Pearson linear correlation was used to test serum NKG2D, IFN-γ, and tumor markers. the serum levels of NKG2D and IFN in different prognosis NSCLC patients were compared to draw the ROC curve, and the value of serum NKG2D, IFN-γ and both combined to predict the prognostic value of NSCLC patients were analyzed.Results Serum NKG2D in stage Ⅲ/Ⅳ group [(67.12 ± 5.28)%] was lower than that in stage I/Ⅱ group [(81.50 ± 7.33)%] (P < 0.05). Serum IFN-γ [(23.67 ± 5.74)ng/mL], CEA [(43.76 ± 6.48)ng/mL], CA125 [(35.62 ± 6.03)u/mL], CYFRA21-1 [ (11.69 ± 1.86) ng/mL] in stage Ⅲ/Ⅳ group were higher than those in stage Ⅲ/Ⅳ group [ (17.91 ± 4.82) ng/mL, (21.53 ± 4.62) ng/mL, (23.59 ± 5.17) u/mL, (6.84 ± 1.12) ng/mL] (P < 0.05); Pearson correlation analysis showed that serum NKG2D was negatively correlated with CEA level (r = -0.683), CA125 level (r = -0.615), and CYFRA21-1 level (r = -0.704) (P < 0.05). IFN-γ was positively correlated with CEA level (r = 0.512), CA125 level (r = 0.439), and CYFRA21-1 level (r = 0.543) (P < 0.05). The overall mortality rate in 150 patients with NSCLC was 22.67%(34/150). The mortality rates within six months in the stage Ⅲ/Ⅳ group were 28.00% (28/100), while those in the stage I/Ⅱ group were 12.00% (6/50) within six months. The difference was statistically significant with χ2 test (χ2 = 4.868, P = 0.027). Serum NKG2D [ (58.58 ± 5.62) % in the death group was lower than that in the non-death group [ (84.23 ± 4.39) %], and serum IFN-γ [ (29.93 ± 3.17) ng/mL] was higher than that in the non-death group [ (20.95 ± 2.20) ng/mL] (P < 0.05). The ROC curve results showed that the AUC of IFN-γ, NKG2D, and both combined outcome prediction outcomes was 0.780 (95% CI: 0.673, 0.942), 0.820 (95% CI: 0.675, 0.955), and 0.860 (95% CI: 0.761, 0.984) in NSCLC patients, respectively; the sensitivity were 78.1% (95% CI: 0.648, 0.892), 82.6% (95% CI: 0.713, 0.955), 86.5% (95% CI: 0.752, 0.978); the specificity were 51.3% (95% CI: 0.443, 0.714), 53.6% (95% CI: 0.467, 0.735), 41.5% (95% CI: 0.328, 0.616).Conclusion The levels of serum NKG2D and IFN-γ are related to the severity of NSCLC and the levels of tumor markers, and the combination of the two can effectively predict the early prognosis of NSCLC.

    表 4 不同预后NSCLC患者的血清NKG2D、IFN-γ比较 (x±s)Table 4
    表 3 NSCLC患者血清NKG2D、IFN-γ与肿瘤标志物的相关性Table 3
    表 1 两组患者血清NKG2D、IFN-γ比较 (x±s)Table 1
    表 5 血清NKG2D、IFN-γ及两者联合对NSCLC患者预后预测的效能分析Table 5
    图1 血清NKG2D、IFN-γ及两者联合对NSCLC患者预后预测价值的ROC曲线图Fig.1
    表 2 两组患者血清肿瘤标志物水平比较 (x±s)Table 2
    参考文献
    [1] 张利诚, 黄良龙, 黄宽. 参一胶囊联合化疗对中晚期非小细胞肺癌患者近期疗效及血清NKG2D、IFN-γ、IL-2水平和T淋巴细胞亚群的影响[J]. 中国老年学杂志, 2020, 40(11): 2296-2299.
    [2] 黄岩, 张力. 2020 CSCO非小细胞肺癌诊疗指南更新要点解读[J]. 临床内科杂志, 2020, 37(8): 603-605.
    [3] AHMED A, TAIT S W G. Targeting immunogenic cell death in cancer[J]. Mol Oncol, 2020, 14(12): 2994-3006.
    [4] 张正富, 向绍华, 李静, 等. 腺苷酸环化酶相关蛋白1在非小细胞肺癌中表达及临床意义[J]. 创伤与急危重病医学, 2020, 8(3): 167-170.
    [5] JHUNJHUNWALA S, HAMMER C, DELAMARRE L. Antigen presentation in cancer: insights into tumour immunogenicity and immune evasion[J]. Nat Rev Cancer, 2021, 21(5): 298-312.
    [6] 中华医学会, 中华医学会肿瘤学分会, 中华医学会杂志社. 中华医学会肺癌临床诊疗指南(2018版)[J]. 肿瘤研究与临床, 2018, 30(12): 793-824.
    [7] CHEN X Z, GAO A Q, ZHANG F, et al. ILT4 inhibition prevents TAM- and dysfunctional T cell-mediated immunosuppression and enhances the efficacy of anti-PD-L1 therapy in NSCLC with EGFR activation[J]. Theranostics, 2021, 11(7): 3392-3416.
    [8] WU S Y, FU T, JIANG Y Z, et al. Natural killer cells in cancer biology and therapy[J]. Mol Cancer, 2020, 19(1): 120.
    [9] 刘亚杰, 马晓波. 肿瘤标志物GSTP1、CYFRA21-1及SCC-Ag对非小细胞肺癌的预后评估价值[J]. 中国现代医学杂志, 2020, 30(14): 42-46.
    [10] LAWSON K A, SOUSA C M, ZHANG X Y, et al. Functional genomic landscape of cancer-intrinsic evasion of killing by T cells[J]. Nature, 2020, 586(7827): 120-126.
    [11] TERANISHI S, KOBAYASHI N, KATAKURA S, et al. Class A CpG oligodeoxynucleotide inhibits IFN-γ-induced signaling and apoptosis in lung cancer[J]. Thorac Cancer, 2020, 11(4): 983-992.
    [12] PAN H Y, CHAI W J, LIU X L, et al. DYNC1H1 regulates NSCLC cell growth and metastasis by IFN-γ-JAK-STAT signaling and is associated with an aberrant immune response[J]. Exp Cell Res, 2021, 409(1): 112897.
    [13] KANAI T, SUZUKI H, YOSHIDA H, et al. Significance of quantitative interferon-gamma levels in non-small-cell lung cancer patients' response to immune checkpoint inhibitors[J]. Anticancer Res, 2020, 40(5): 2787-2793.
    [14] 段素华, 王素梅. 血清CYFRA21-1、CEA、CA125联合检测在非小细胞肺癌中的诊断价值[J]. 实用临床医药杂志, 2020, 24(8): 55-57.
    [15] YU M, PENG Z X, QIN M, et al. Interferon-γ induces tumor resistance to anti-PD-1 immunotherapy by promoting YAP phase separation[J]. Mol Cell, 2021, 81(6): 1216-1230.e9.
    [16] 李玲, 谢明水, 邓涛, 等. 血清CEA、SCCA、CYFRA21-1对非小细胞肺癌和5年预后的联合诊断价值[J]. 湖北医药学院学报, 2021, 40(4): 332-337.
    [17] POCKLEY A G, VAUPEL P, MULTHOFF G. NK cell-based therapeutics for lung cancer[J]. Expert Opin Biol Ther, 2020, 20(1): 23-33.
    [18] 张靖悦, 郑光辉, 杨常建, 等. 非小细胞肺癌患者外周血自然杀伤细胞受体表达及与肿瘤标志物的关系研究[J]. 癌症进展, 2022, 20(3): 290-293.
    [19] 钟家将, 张东伟, 蓝冰, 等. 人类表皮生长因子受体2、β2-微球蛋白、鳞状细胞癌相关抗原对非小细胞肺癌诊断价值研究[J]. 临床军医杂志, 2020, 48(7): 830-831.
    [20] INGRAM Z, MADAN S, MERCHANT J, et al. Targeting natural killer T cells in solid malignancies[J]. Cells, 2021, 10(6): 1329.
    [21] KANG Y T, NIU Z Q, HADLOCK T, et al. On-chip biogenesis of circulating NK cell-derived exosomes in non-small cell lung cancer exhibits antitumoral activity[J]. Adv Sci (Weinh), 2021, 8(6): 2003747.
    [22] LEE K S, CHUNG W Y, PARK J E, et al. Interferon-γ-inducible chemokines as prognostic markers for lung cancer[J]. Int J Environ Res Public Health, 2021, 18(17): 9345.
    [23] OKITA R, MAEDA A, SHIMIZU K, et al. Clinicopathological relevance of tumor expression of NK group 2 member D ligands in resected non-small cell lung cancer[J]. Oncotarget, 2019, 10(63): 6805-6815.
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李艳光,宋翔,牛洁婷,唐国杰.血清NK细胞活化性受体、γ干扰素与非小细胞肺癌患者病情程度、预后的相关性分析[J].中国现代医学杂志,2022,(23):67-72

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  • 收稿日期:2022-06-14
  • 在线发布日期: 2023-10-23
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