• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

CD36在胰腺腺癌中的低表达及其与临床病理特征和预后的相关性。

Down-expression of CD36 in pancreatic adenocarcinoma and its correlation with clinicopathological features and prognosis.

作者信息

Jia Shengnan, Zhou Liangjing, Shen Tao, Zhou Senhao, Ding Guoping, Cao Liping

机构信息

Department of General Surgery, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, No. 3, Qingchun Road, Hangzhou, China.

出版信息

J Cancer. 2018 Jan 1;9(3):578-583. doi: 10.7150/jca.21046. eCollection 2018.

DOI:10.7150/jca.21046
PMID:29483963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5820925/
Abstract

Recent studies show that CD36 plays a key role in the occurrence and development of tumors, especially in the metastasis of tumors. However, the expression and role of CD36 has not been reported in pancreatic cancer. This study is aimed to explore the expression of CD36 in pancreatic cancer and corresponding non-tumor normal tissues, and its correlation with clinicopathological features and prognosis of pancreatic cancer patients. By analyzing the chip results of database GSE16515, we found that there was significant differential expression of CD36 in pancreatic cancer and corresponding non-tumor normal tissues. In this study, western blot and immunohistochemistry were used to show that the expression of CD36 in pancreatic cancer cells and tissues is significantly lower than that in corresponding non-tumor normal tissues. By statistically analyzing clinical and pathological data, we found that low expression of CD36 predicts lower TNM staging and CA19-9 levels, but larger tumor size and poor survival prognosis. These findings indicated that CD36 can be used as a predictor of clinicopathological features and prognosis, but the contradiction is worthy of our further study.

摘要

最近的研究表明,CD36在肿瘤的发生和发展中起关键作用,尤其是在肿瘤转移方面。然而,CD36在胰腺癌中的表达及作用尚未见报道。本研究旨在探讨CD36在胰腺癌及相应非肿瘤正常组织中的表达情况,及其与胰腺癌患者临床病理特征和预后的相关性。通过分析数据库GSE16515的芯片结果,我们发现CD36在胰腺癌及相应非肿瘤正常组织中存在显著差异表达。在本研究中,采用蛋白质印迹法和免疫组织化学法显示,CD36在胰腺癌细胞和组织中的表达明显低于相应的非肿瘤正常组织。通过对临床和病理数据进行统计分析,我们发现CD36低表达预示着较低的TNM分期和CA19-9水平,但肿瘤体积较大且生存预后较差。这些发现表明,CD36可作为临床病理特征和预后的预测指标,但其中的矛盾之处值得我们进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/602d/5820925/92ea73e091e1/jcav09p0578g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/602d/5820925/8b66019202d0/jcav09p0578g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/602d/5820925/2e0c92b52dbc/jcav09p0578g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/602d/5820925/92ea73e091e1/jcav09p0578g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/602d/5820925/8b66019202d0/jcav09p0578g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/602d/5820925/2e0c92b52dbc/jcav09p0578g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/602d/5820925/92ea73e091e1/jcav09p0578g003.jpg

相似文献

1
Down-expression of CD36 in pancreatic adenocarcinoma and its correlation with clinicopathological features and prognosis.CD36在胰腺腺癌中的低表达及其与临床病理特征和预后的相关性。
J Cancer. 2018 Jan 1;9(3):578-583. doi: 10.7150/jca.21046. eCollection 2018.
2
Expression of DEK in pancreatic cancer and its correlation with clinicopathological features and prognosis.DEK在胰腺癌中的表达及其与临床病理特征和预后的相关性。
J Cancer. 2019 Jan 29;10(4):911-917. doi: 10.7150/jca.27405. eCollection 2019.
3
The up-regulation of Axl is associated with a poor prognosis and promotes proliferation in pancreatic ductal adenocarcinoma.Axl的上调与预后不良相关,并促进胰腺导管腺癌的增殖。
Int J Clin Exp Pathol. 2019 May 1;12(5):1626-1633. eCollection 2019.
4
Sulfatase 1 expression in pancreatic cancer and its correlation with clinicopathological features and postoperative prognosis.磺基转移酶 1 在胰腺癌中的表达及其与临床病理特征和术后预后的关系。
Cancer Biomark. 2018;22(4):701-707. doi: 10.3233/CBM-181210.
5
Ezrin protein overexpression predicts the poor prognosis of pancreatic ductal adenocarcinomas.埃兹蛋白过表达预示胰腺导管腺癌预后不良。
Exp Mol Pathol. 2015 Feb;98(1):1-6. doi: 10.1016/j.yexmp.2014.11.003. Epub 2014 Nov 5.
6
Glypican-3 and KRT19 are markers associating with metastasis and poor prognosis of pancreatic ductal adenocarcinoma.磷脂酰肌醇蛋白聚糖-3和细胞角蛋白19是与胰腺导管腺癌转移及预后不良相关的标志物。
Cancer Biomark. 2016;17(4):397-404. doi: 10.3233/CBM-160655.
7
High Expression of P38α and Preoperative Carbohydrate Antigen 19-9 Indicate Poor Prognosis in Patients with Pancreatic Ductal Adenocarcinoma.P38α高表达及术前糖类抗原19-9提示胰腺导管腺癌患者预后不良。
J Cancer. 2018 Jan 6;9(4):650-659. doi: 10.7150/jca.21683. eCollection 2018.
8
AQP1 and AQP3 Expression are Associated With Severe Symptoms and Poor-prognosis of the Pancreatic Ductal Adenocarcinoma.水通道蛋白1和水通道蛋白3的表达与胰腺导管腺癌的严重症状及不良预后相关。
Appl Immunohistochem Mol Morphol. 2019 Jan;27(1):40-47. doi: 10.1097/PAI.0000000000000523.
9
Relationship between S100A4 protein expression and pre-operative serum CA19.9 levels in pancreatic carcinoma and its prognostic significance.胰腺癌中 S100A4 蛋白表达与术前血清 CA19.9 水平的关系及其预后意义。
World J Surg Oncol. 2019 Sep 16;17(1):163. doi: 10.1186/s12957-019-1707-4.
10
High Expression of Cell Division Cycle 42 Promotes Pancreatic Cancer Growth and Predicts Poor Outcome of Pancreatic Cancer Patients.细胞分裂周期蛋白42的高表达促进胰腺癌生长并预示胰腺癌患者预后不良。
Dig Dis Sci. 2017 Apr;62(4):958-967. doi: 10.1007/s10620-017-4451-z. Epub 2017 Feb 8.

引用本文的文献

1
Proteomic meta-analysis unveils new frontiers for biomarkers research in pancreatic carcinoma.蛋白质组学荟萃分析揭示了胰腺癌生物标志物研究的新前沿。
Oncogenesis. 2025 Feb 16;14(1):3. doi: 10.1038/s41389-025-00547-4.
2
Dysregulation of genes involved in the long-chain fatty acid transport in pancreatic ductal adenocarcinoma.胰腺导管腺癌中长链脂肪酸转运相关基因的失调。
World J Gastrointest Oncol. 2025 Jan 15;17(1):98409. doi: 10.4251/wjgo.v17.i1.98409.
3
Lipid Metabolism as a Potential Target of Liver Cancer.脂质代谢作为肝癌的潜在靶点。

本文引用的文献

1
Linking Metabolic Dysfunction to Atherosclerosis Via Activation of Macrophage CD36 Gene Transcription by Retinol Binding Protein-4.通过视黄醇结合蛋白-4激活巨噬细胞CD36基因转录将代谢功能障碍与动脉粥样硬化联系起来
Circulation. 2017 Apr 4;135(14):1355-1356. doi: 10.1161/CIRCULATIONAHA.117.027505.
2
Platelet CD36 promotes thrombosis by activating redox sensor ERK5 in hyperlipidemic conditions.在高脂血症条件下,血小板CD36通过激活氧化还原传感器ERK5促进血栓形成。
Blood. 2017 May 25;129(21):2917-2927. doi: 10.1182/blood-2016-11-750133. Epub 2017 Mar 23.
3
From fat to FAT (CD36/SR-B2): Understanding the regulation of cellular fatty acid uptake.
J Hepatocell Carcinoma. 2024 Feb 14;11:327-346. doi: 10.2147/JHC.S450423. eCollection 2024.
4
Inside anticancer therapy resistance and metastasis. Focus on CD36.抗癌治疗耐药性与转移机制。聚焦于CD36。
J Cancer. 2024 Jan 27;15(6):1675-1686. doi: 10.7150/jca.90457. eCollection 2024.
5
Unveiling Disrupted Lipid Metabolism in Benign Prostate Hyperplasia, Prostate Cancer, and Metastatic Patients: Insights from a Colombian Nested Case-Control Study.揭示良性前列腺增生、前列腺癌和转移患者中脂质代谢紊乱:来自哥伦比亚巢式病例对照研究的见解
Cancers (Basel). 2023 Nov 18;15(22):5465. doi: 10.3390/cancers15225465.
6
Protein Kinase D1 Signaling in Cancer Stem Cells with Epithelial-Mesenchymal Plasticity.蛋白激酶 D1 信号在具有上皮-间充质转化的肿瘤干细胞中的作用。
Cells. 2022 Dec 1;11(23):3885. doi: 10.3390/cells11233885.
7
CD36-Fatty Acid-Mediated Metastasis via the Bidirectional Interactions of Cancer Cells and Macrophages.CD36 通过癌细胞和巨噬细胞的双向相互作用介导脂肪酸转移。
Cells. 2022 Nov 10;11(22):3556. doi: 10.3390/cells11223556.
8
Lipid metabolism in pancreatic cancer: emerging roles and potential targets.胰腺癌中的脂代谢:新出现的作用和潜在靶点。
Cancer Commun (Lond). 2022 Dec;42(12):1234-1256. doi: 10.1002/cac2.12360. Epub 2022 Sep 15.
9
Genome-Wide Histone H3K27 Acetylation Profiling Identified Genes Correlated With Prognosis in Papillary Thyroid Carcinoma.全基因组组蛋白H3K27乙酰化谱分析鉴定出与甲状腺乳头状癌预后相关的基因。
Front Cell Dev Biol. 2021 Jun 11;9:682561. doi: 10.3389/fcell.2021.682561. eCollection 2021.
10
The value of a metabolic reprogramming-related gene signature for pancreatic adenocarcinoma prognosis prediction.代谢重编程相关基因特征对胰腺腺癌预后预测的价值。
Aging (Albany NY). 2020 Nov 20;12(23):24228-24241. doi: 10.18632/aging.104134.
从脂肪到FAT(CD36/SR-B2):理解细胞脂肪酸摄取的调控
Biochimie. 2017 May;136:21-26. doi: 10.1016/j.biochi.2016.12.007. Epub 2016 Dec 22.
4
High-density lipoprotein from subjects with coronary artery disease promotes macrophage foam cell formation: role of scavenger receptor CD36 and ERK/MAPK signaling.来自冠心病患者的高密度脂蛋白促进巨噬细胞泡沫细胞形成:清道夫受体CD36和ERK/MAPK信号传导的作用
Mol Cell Biochem. 2017 Mar;427(1-2):23-34. doi: 10.1007/s11010-016-2895-7. Epub 2016 Dec 19.
5
Targeting metastasis-initiating cells through the fatty acid receptor CD36.通过脂肪酸受体 CD36 靶向转移起始细胞。
Nature. 2017 Jan 5;541(7635):41-45. doi: 10.1038/nature20791. Epub 2016 Dec 7.
6
CD36 Provides Host Protection Against Klebsiella pneumoniae Intrapulmonary Infection by Enhancing Lipopolysaccharide Responsiveness and Macrophage Phagocytosis.CD36通过增强脂多糖反应性和巨噬细胞吞噬作用为宿主提供针对肺炎克雷伯菌肺部感染的保护。
J Infect Dis. 2016 Dec 15;214(12):1865-1875. doi: 10.1093/infdis/jiw451. Epub 2016 Sep 28.
7
Inhibition of Macrophage CD36 Expression and Cellular Oxidized Low Density Lipoprotein (oxLDL) Accumulation by Tamoxifen: A PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR)γ-DEPENDENT MECHANISM.他莫昔芬对巨噬细胞CD36表达及细胞内氧化型低密度脂蛋白(oxLDL)蓄积的抑制作用:一种过氧化物酶体增殖物激活受体(PPAR)γ依赖机制
J Biol Chem. 2016 Aug 12;291(33):16977-89. doi: 10.1074/jbc.M116.740092. Epub 2016 Jun 29.
8
Chemokine Signaling Enhances CD36 Responsiveness toward Oxidized Low-Density Lipoproteins and Accelerates Foam Cell Formation.趋化因子信号增强了 CD36 对氧化型低密度脂蛋白的反应性,并加速了泡沫细胞的形成。
Cell Rep. 2016 Mar 29;14(12):2859-71. doi: 10.1016/j.celrep.2016.02.071. Epub 2016 Mar 17.
9
Pancreatic cancer.胰腺癌。
Lancet. 2016 Jul 2;388(10039):73-85. doi: 10.1016/S0140-6736(16)00141-0. Epub 2016 Jan 30.
10
Extracellular Vesicles Activate a CD36-Dependent Signaling Pathway to Inhibit Microvascular Endothelial Cell Migration and Tube Formation.细胞外囊泡激活依赖CD36的信号通路以抑制微血管内皮细胞迁移和管腔形成。
Arterioscler Thromb Vasc Biol. 2016 Mar;36(3):534-44. doi: 10.1161/ATVBAHA.115.307085. Epub 2016 Jan 28.