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合并与未合并糖尿病的胰腺癌患者血管生成素样蛋白2在血清中的表达及其与预后的关系

秦雯 陈泰文 郑海平 黄夏宁 朱小东

引用本文:
Citation:

合并与未合并糖尿病的胰腺癌患者血管生成素样蛋白2在血清中的表达及其与预后的关系

DOI: 10.3969/j.issn.1001-5256.2021.06.034
基金项目: 

国家自然科学基金 (81860508);

广西自然科学基金 (2018GXNSFAA138026);

广西医疗卫生适宜技术开发与推广应用项目 (S2018040);

广西壮族自治区卫生和计划生育委员会自筹经费科研课题 (Z20180950);

南宁市武鸣区科学研究与技术开发计划项目 (20190403)

利益冲突声明:本研究不存在研究者、伦理委员会成员、受试者监护人以及与公开研究成果有关的利益冲突。
作者贡献声明:秦雯负责课题设计,资料分析,撰写论文;陈泰文、郑海平参与收集数据和样本,进行统计分析;黄夏宁负责血清ELISA测定血清ANGPTL2浓度的实验操作及统计学分析;朱小东指导撰写文章并最后定稿。
详细信息
    作者简介:

    秦雯(1980—),女,博士,副教授,主要从事肿瘤分子病理学方面的研究

    通信作者:

    朱小东,zhuxiaodong@gxmu.edu.cn

  • 中图分类号: R735.9

Serum expression of angiopoietin-like protein 2 in pancreatic cancer patients with or without diabetes and its association with prognosis

  • 摘要:   目的  探讨血管生成素样蛋白2(ANGPTL2)在合并与未合并糖尿病的胰腺癌患者中的表达水平及其作为胰腺癌患者预后指标的价值。  方法  收集2015年1月—2018年1月于广西医科大学第一附属医院、广西医科大学附属肿瘤医院、广西医科大学附属武鸣医院治疗的胰腺癌患者的血清标本125例,其中单纯胰腺癌组64例、合并糖尿病胰腺癌组61例,另选取66例健康体检者作为对照组。采用ELISA法检测各组血清ANGPTL2水平,分析ANGPTL2的表达水平与临床指标、生存预后的关系。符合正态分布的计量资料3组间比较采用单因素方差分析,进一步两两比较采用Bonferroni法;偏态分布者的计量资料3组间比较采用独立样本Kruskal-Wallis H秩和检验,进一步两两比较采用单因素ANOVA法。计数资料组间比较采用χ2检验。相关性分析采用Spearman相关分析。Kaplan-Meier法绘制生存曲线,log-rank检验比较生存率。采用Cox风险模型行单/多因素分析,确定影响胰腺癌预后的独立危险因素。  结果  合并糖尿病胰腺癌组患者血清ANGPTL2[7.79(7.12~8.17) ng/ml]明显高于单纯胰腺癌组[5.74(5.08~6.40) ng/ml]和健康对照组[3.72(3.25~4.16) ng/ml](P值均<0.001)。血清ANGPTL2水平与CA19-9、CEA均呈正相关(r值分别为0.560、0.731,P值均<0.001)。单因素分析显示,肿瘤大小、远处器官转移、分化程度、CEA、ANGPTL2、HbA1c与胰腺癌患者远期生存密切相关(P值均<0.05);多因素分析显示,肿瘤大小(HR=2.657,P=0.005)、远处器官转移(HR=5.000,P=0.014)、分化程度(HR=2.466, P=0.004)、CEA(HR=1.110,P<0.001)、ANGPTL2(HR=1.901,P=0.001)均为影响胰腺癌患者预后的独立危险因素。在所有胰腺癌患者中,ANGPTL2高表达组的2年生存率明显低于ANGPTL2低表达组(8.51% vs 25.81%,χ2=5.651,P=0.017)。在合并糖尿病的胰腺癌患者中ANGPTL2高表达组的2年生存率也明显低于ANGPTL2低表达组(2.20% vs 32.70%, χ2=24.895,P<0.001)。  结论  ANGPTL2可能是评价胰腺癌患者,特别是合并糖尿病的胰腺癌患者预后的有效指标。

     

  • 图  1  胰腺癌患者血清ANGPTL2与CA19-9的相关性分析

    图  2  胰腺癌患者血清ANGPTL2与CEA的相关性分析

    图  3  ANGPTL2高/低表达组胰腺癌患者的生存曲线

    图  4  单纯胰腺癌组与合并糖尿病胰腺癌组患者的生存曲线

    表  1  3组一般资料比较

    项目 单纯胰腺癌组(n=64) 合并糖尿病胰腺癌组(n=61) 健康对照组(n=66) 统计值 P
    年龄(岁) 63.08±8.25 61.00±8.23 62.91±8.78 F=1.166 0.314
    性别(男/女) 35/29 34/27 36/30 χ2=0.021 0.989
    BMI(kg/m2) 24.29±1.92 23.40±2.05 25.16±2.00 F=12.371 <0.001
    HbA1c(%) 5.50±0.29 8.28±0.59 5.27±0.16 F=119.6 <0.001
    CRP(mg/dl) 1.61±0.68 1.85±0.621) 0.25±0.12 F=170.022 <0.001
    TC(mg/dl) 178.17±22.61 167.78±22.661)2) 186.00±22.34 F=10.394 <0.001
    TG(mg/dl) 119.59±28.62 122.67±26.431) 97.59±25.55 F=16.696 <0.001
    注:1)与健康对照组比较,P<0.05;2)与单纯胰腺癌组比较,P<0.05。
    下载: 导出CSV

    表  2  3组人群血清CEA、CA19-9及ANGPTL2水平比较

    组别 例数 CEA(ng/ml) CA19-9(U/ml) ANGPTL2(ng/ml)
    单纯胰腺癌组 64 14.71(9.07~24.07) 83.11(40.85~109.77) 5.74(5.08~6.40)
    合并糖尿病胰腺癌组 61 30.43(18.99~37.12) 130.45(98.62~214.01) 7.79(7.12~8.17)
    健康对照组 66 2.01(1.42~2.93) 13.08(9.03~19.60) 3.72(3.25~4.16)
    χ2 135.7011) 114.5181) 126.3671)
    P <0.001 <0.001 <0.001
    注: 组间两两比较,1)P值均<0.05。
    下载: 导出CSV

    表  3  影响胰腺癌患者远期生存的单因素分析

    因素 β HR 95%CI P
    肿瘤大小 1.126 3.084 1.504~6.324 0.002
    血管侵犯 -0.571 0.565 0.210~1.520 0.258
    神经侵犯 -0.015 0.985 0.374~2.595 0.975
    淋巴结转移 0.826 2.283 0.904~5.765 0.081
    远处器官转移 1.719 5.577 1.472~21.135 0.011
    分化程度 0.928 2.530 1.347~4.752 0.004
    CA199(U/ml) 0.000 1.000 0.994~1.006 0.912
    CEA(ng/ml) 0.131 1.140 1.070~1.215 <0.001
    CRP(mg/dl) -0.353 0.703 0.356~1.389 0.310
    ANGPTL2(ng/ml) 0.584 1.793 1.224~2.628 0.003
    HbA1c(%) 0.653 1.903 1.354~2.873 0.003
    下载: 导出CSV

    表  4  影响胰腺癌患者远期生存的多因素分析

    因素 HR 95%CI P
    肿瘤大小 2.657 1.338~5.276 0.005
    远处器官转移 5.000 1.380~18.114 0.014
    分化程度 2.466 1.344~4.522 0.004
    CEA 1.110 1.056~1.167 <0.001
    ANGPTL2 1.901 1.310~2.759 0.001
    下载: 导出CSV

    表  5  血清ANGPTL2表达水平、是否合并糖尿病与胰腺癌患者预后的关系

    参数 例数 2年生存率(%) χ2 P
    ANGPTL2 5.651 0.017
      高表达组 94 8.51
      低表达组 31 25.81
    HbA1c 0.621 0.431
      升高 61 8.20
      正常 64 12.50
    下载: 导出CSV
  • [1] ANTOLINO L, ROCCA M, TODDE F, et al. Can pancreatic cancer be detected by adrenomedullin in patients with new-onset diabetes? The PaCANOD cohort study protocol[J]. Tumori, 2018, 104(4): 312-314. DOI: 10.5301/tj.5000693.
    [2] ZHANG Z, QIN W, SUN Y. Contribution of biomarkers for pancreatic cancer-associated new-onset diabetes to pancreatic cancer screening[J]. Pathol Res Pract, 2018, 214(12): 1923-1928. DOI: 10.1016/j.prp.2018.10.003.
    [3] RISCH HA. Diabetes and pancreatic cancer: Both cause and effect[J]. J Natl Cancer Inst, 2019, 111(1): 1-2. DOI: 10.1093/jnci/djy093.
    [4] KADOMATSU T, ENDO M, MIYATA K, et al. Diverse roles of ANGPTL2 in physiology and pathophysiology[J]. Trends Endocrinol Metab, 2014, 25(5): 245-254. DOI: 10.1016/j.tem.2014.03.012.
    [5] KIM I, KWAK HJ, AHN JE, et al. Molecular cloning and characterization of a novel angiopoietin family protein, angiopoietin-3[J]. FEBS Lett, 1999, 443(3): 353-356. DOI: 10.1016/s0014-5793(99)00008-3.
    [6] KENAWY MZ, SABRY JH, AKL EM, et al. Angiopoietin-like protein 2 in psoriasis: A new linkage with metabolic syndrome[J]. Postepy Dermatol Alergol, 2020, 37(1): 86-91. DOI: 10.5114/ada.2018.79225.
    [7] WANG X, HU Z, WANG Z, et al. Angiopoietin-like protein 2 is an important facilitator of tumor proliferation, metastasis, angiogenesis and glycolysis in osteosarcoma[J]. Am J Transl Res, 2019, 11(10): 6341-6355. http://www.ncbi.nlm.nih.gov/pubmed/31737187
    [8] HE J, XU J, YU X, et al. Overexpression of ANGPTL2 and LILRB2 as predictive and therapeutic biomarkers for metastasis and prognosis in colorectal cancer[J]. Int J Clin Exp Pathol, 2018, 11(5): 2281-2294. http://www.ncbi.nlm.nih.gov/pubmed/31938340
    [9] ABBASZADEH Z, ÇEŞMELI S, BIRAY AÇ. Crucial players in glycolysis: Cancer progress[J]. Gene, 2020, 726: 144158. DOI: 10.1016/j.gene.2019.144158.
    [10] YOSHINAGA T, NIOU T, NⅡHARA T, et al. Angiopoietin-like protein 2 is a useful biomarker for pancreatic cancer that is associated with type 2 diabetes mellitus and inflammation[J]. J Cancer, 2018, 9(24): 4736-4741. DOI: 10.7150/jca.25404.
    [11] WANG Y, ZHENG Z, YANG Y, et al. Angiopoietin-like 2 is a potential biomarker for diabetic foot patients[J]. BMC Endocr Disord, 2020, 20(1): 178. DOI: 10.1186/s12902-020-00657-7.
    [12] BOURSI B, FINKELMAN B, GIANTONIO BJ, et al. A clinical prediction model to assess risk for pancreatic cancer among patients with prediabetes[J]. Eur J Gastroenterol Hepatol, 2021. DOI: 10.1097/MEG.0000000000002052.[Online ahead of print]
    [13] ANDERSEN DK, KORC M, PETERSEN GM, et al. Diabetes, pancreatogenic diabetes, and pancreatic cancer[J]. Diabetes, 2017, 66(5): 1103-1110. DOI: 10.2337/db16-1477.
    [14] PIZZATO M, TURATI F, ROSATO V, et al. Exploring the link between diabetes and pancreatic cancer[J]. Expert Rev Anticancer Ther, 2019, 19(8): 681-687. DOI: 10.1080/14737140.2019.1642109.
    [15] TABATA M, KADOMATSU T, FUKUHARA S, et al. Angiopoietin-like protein 2 promotes chronic adipose tissue inflammation and obesity-related systemic insulin resistance[J]. Cell Metab, 2009, 10(3): 178-188. DOI: 10.1016/j.cmet.2009.08.003.
    [16] FARHAT N, THORIN-TRESCASES N, MAMARBACHI M, et al. Angiopoietin-like 2 promotes atherogenesis in mice[J]. J Am Heart Assoc, 2013, 2(3): e000201. DOI: 10.1161/JAHA.113.000201.
    [17] TAZUME H, MIYATA K, TIAN Z, et al. Macrophage-derived angiopoietin-like protein 2 accelerates development of abdominal aortic aneurysm[J]. Arterioscler Thromb Vasc Biol, 2012, 32(6): 1400-1409. DOI: 10.1161/ATVBAHA.112.247866.
    [18] OGATA A, ENDO M, AOI J, et al. The role of angiopoietin-like protein 2 in pathogenesis of dermatomyositis[J]. Biochem Biophys Res Commun, 2012, 418(3): 494-499. DOI: 10.1016/j.bbrc.2012.01.052.
    [19] ENDO M, NAKANO M, KADOMATSU T, et al. Tumor cell-derived angiopoietin-like protein ANGPTL2 is a critical driver of metastasis[J]. Cancer Res, 2012, 72(7): 1784-1794. DOI: 10.1158/0008-5472.CAN-11-3878.
    [20] CHEN Y, JIANG H, ZHU L, et al. Diagnostic and prognostic value of serum angiopoietin-like protein 2 in patients with non-small cell lung cancer[J]. Clin Lab, 2017, 63(1): 59-65. DOI: 10.7754/Clin.Lab.2016.160528.
    [21] OSUMI H, HORIGUCHI H, KADOMATSU T, et al. Tumor cell-derived angiopoietin-like protein 2 establishes a preference for glycolytic metabolism in lung cancer cells[J]. Cancer Sci, 2020, 111(4): 1241-1253. DOI: 10.1111/cas.14337.
    [22] YANG L, SUN R, WANG Y, et al. Expression of ANGPTL2 and its impact on papillary thyroid cancer[J]. Cancer Cell Int, 2019, 19: 204. DOI: 10.1186/s12935-019-0908-9.
    [23] YOSHINAGA T, NISHIMATA H, TANAKA S, et al. Use of ANGPTL2 mRNA levels in formalin-fixed paraffin-embedded tissues as a biomarker to diagnose gastric cancer and to evaluate the extent of vascular invasion[J]. Oncol Lett, 2019, 17(1): 518-524. DOI: 10.3892/ol.2018.9610.
    [24] HUANG D, SUN G, HAO X, et al. ANGPTL2-containing small extracellular vesicles from vascular endothelial cells accelerate leukemia progression[J]. J Clin Invest, 2021, 131(1): e138986. DOI: 10.1172/JCI138986.
    [25] CARBONE C, MOCCIA T, ZHU C, et al. Anti-VEGF treatment-resistant pancreatic cancers secrete proinflammatory factors that contribute to malignant progression by inducing an EMT cell phenotype[J]. Clin Cancer Res, 2011, 17(17): 5822-5832. DOI: 10.1158/1078-0432.CCR-11-1185.
    [26] CARBONE C, PIRO G, FASSAN M, et al. An angiopoietin-like protein 2 autocrine signaling promotes EMT during pancreatic ductal carcinogenesis[J]. Oncotarget, 2015, 6(15): 13822-13834. DOI: 10.18632/oncotarget.2635.
    [27] CHEN H, LI T, WANG ZJ, et al. Influence of metabolic syndrome and its components on the prognosis of patients with pancreatic cancer[J]. J Clin Hepatol, 2020, 36(12): 2788-2794. DOI: 10.3969/j.issn.1001-5256.2020.12.029.

    陈欢, 李婷, 王紫洁, 等. 代谢综合征及其组分对胰腺癌患者预后的影响[J]. 临床肝胆病杂志, 2020, 36(12): 2788-2794. DOI: 10.3969/j.issn.1001-5256.2020.12.029.
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  • 收稿日期:  2021-02-02
  • 录用日期:  2021-03-15
  • 出版日期:  2021-06-20
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