• 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

研究 CXCR4、CXCL12、CD44 和 CD147 的表达水平及其与垂体腺瘤侵袭行为的潜在相关性。

Study on the expression levels of CXCR4, CXCL12, CD44, and CD147 and their potential correlation with invasive behaviors of pituitary adenomas.

机构信息

Departments of Neurosurgery, Key Laboratory of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.

出版信息

Biomed Environ Sci. 2013 Jul;26(7):592-8. doi: 10.3967/0895-3988.2013.07.011.

DOI:10.3967/0895-3988.2013.07.011
PMID:23895705
Abstract

OBJECTIVE

To evaluate the factors of CXCR4, CXCL12, CD44, and CD147 as early potential diagnostic biomarkers by determining their expression levels in invasive and non-invasive pituitary adenomas.

METHODS

Fresh pituitary adenoma specimens were collected from 35 pituitary adenoma (21 invasive and 14 non-invasive) patients who underwent surgical treatment in our Neurosurgery Department between January and April of 2009. The expression levels of CXCR4, CXCL12, CD44, and CD147 were evaluated firstly by flow cytometry, fluorescence microscopy in single cell suspensions, and then by immunohistochemical staining of paraffin tissue sections.

RESULTS

Flow cytometric analyses showed that the percentage of CXCR4- and CXCL12-positive cells from invasive pituitary adenomas (IPA) was significantly higher in the single cell suspensions than that from non-invasive pituitary adenomas (nIPA) (P<0.05). Immunohistochemical staining revealed that CXCR4 and CXCL12 staining index scores of the invasive pituitary adenomas were significantly higher than those of the non-invasive pituitary adenomas (P<0.05). In contrast, neither flow cytometry nor immunohistochemical staining demonstrated significant difference between CD44 and CD147 expression levels, respectively.

CONCLUSION

Expression levels of CXCR4 and CXCL12 are correlated with the invasiveness of pituitary adenomas. Therefore, rather than CD44 and CD147, CXCR4 and CXCL12 may potentially serve as biomarkers for early detection of pituitary adenomas.

摘要

目的

通过检测 CXCR4、CXCL12、CD44 和 CD147 在侵袭性和非侵袭性垂体腺瘤中的表达水平,评估其作为早期潜在诊断生物标志物的因素。

方法

收集 2009 年 1 月至 4 月在我院神经外科接受手术治疗的 35 例垂体腺瘤(21 例侵袭性和 14 例非侵袭性)患者的新鲜垂体腺瘤标本。首先通过流式细胞术、单细胞悬液荧光显微镜和石蜡组织切片免疫组织化学染色评估 CXCR4、CXCL12、CD44 和 CD147 的表达水平。

结果

流式细胞术分析显示,侵袭性垂体腺瘤(IPA)单细胞悬液中 CXCR4 和 CXCL12 阳性细胞的百分比明显高于非侵袭性垂体腺瘤(nIPA)(P<0.05)。免疫组织化学染色显示,侵袭性垂体腺瘤中 CXCR4 和 CXCL12 的染色指数评分明显高于非侵袭性垂体腺瘤(P<0.05)。相比之下,流式细胞术和免疫组织化学染色均未显示 CD44 和 CD147 的表达水平存在显著差异。

结论

CXCR4 和 CXCL12 的表达水平与垂体腺瘤的侵袭性相关。因此,CXCR4 和 CXCL12 可能比 CD44 和 CD147 更能作为垂体腺瘤早期检测的潜在生物标志物。

相似文献

1
Study on the expression levels of CXCR4, CXCL12, CD44, and CD147 and their potential correlation with invasive behaviors of pituitary adenomas.研究 CXCR4、CXCL12、CD44 和 CD147 的表达水平及其与垂体腺瘤侵袭行为的潜在相关性。
Biomed Environ Sci. 2013 Jul;26(7):592-8. doi: 10.3967/0895-3988.2013.07.011.
2
The CXCR4 antagonist AMD3100 suppresses hypoxia-mediated growth hormone production in GH3 rat pituitary adenoma cells.CXCR4 拮抗剂 AMD3100 抑制 GH3 大鼠垂体腺瘤细胞缺氧介导的生长激素产生。
J Neurooncol. 2010 Oct;100(1):51-64. doi: 10.1007/s11060-010-0152-6. Epub 2010 Mar 23.
3
CD147 expression in pituitary adenomas and its significance for clinical outcome.CD147 在垂体腺瘤中的表达及其对临床转归的意义。
Hum Pathol. 2010 Aug;41(8):1165-71. doi: 10.1016/j.humpath.2009.10.023. Epub 2010 Apr 8.
4
Cancer stem cell and its niche in malignant progression of oral potentially malignant disorders.口腔潜在恶性疾病恶性进展中的癌症干细胞及其龛位。
Oral Oncol. 2017 Dec;75:140-147. doi: 10.1016/j.oraloncology.2017.11.003. Epub 2017 Nov 12.
5
Overexpression of stromal cell-derived factor 1 and its receptor CXCR4 induces autocrine/paracrine cell proliferation in human pituitary adenomas.基质细胞衍生因子1及其受体CXCR4的过表达诱导人垂体腺瘤中的自分泌/旁分泌细胞增殖。
Clin Cancer Res. 2008 Aug 15;14(16):5022-32. doi: 10.1158/1078-0432.CCR-07-4717.
6
Changes in CXCL12/CXCR4-chemokine expression during onset of colorectal malignancies.结直肠癌发生过程中CXCL12/CXCR4趋化因子表达的变化
Tumour Biol. 2011 Feb;32(1):189-96. doi: 10.1007/s13277-010-0112-y. Epub 2010 Sep 24.
7
Interstitial flow differentially increases patient-derived glioblastoma stem cell invasion via CXCR4, CXCL12, and CD44-mediated mechanisms.间质流通过CXCR4、CXCL12和CD44介导的机制差异性地增加患者来源的胶质母细胞瘤干细胞侵袭。
Integr Biol (Camb). 2016 Dec 5;8(12):1246-1260. doi: 10.1039/c6ib00167j.
8
[Differential expression of DJ-1 and HSP27 in invasive and non-invasive pituitary adenomas].
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2012 May;37(5):481-4. doi: 10.3969/j.issn.1672-7347.2012.05.009.
9
The relationship between MRI invasive features and expression of EMMPRIN, galectin-3, and microvessel density in pituitary adenoma.垂体腺瘤中 MRI 侵袭特征与 EMMPRIN、半乳糖凝集素-3 和微血管密度表达的关系。
Clin Imaging. 2011 May-Jun;35(3):165-73. doi: 10.1016/j.clinimag.2010.06.002.
10
Identification of a subtype-specific ENC1 gene related to invasiveness in human pituitary null cell adenoma and oncocytomas.在人类垂体无功能细胞腺瘤和嗜酸细胞瘤中鉴定与侵袭性相关的亚型特异性ENC1基因。
J Neurooncol. 2014 Sep;119(2):307-15. doi: 10.1007/s11060-014-1479-1. Epub 2014 Jun 11.

引用本文的文献

1
Research status and prospects of pituitary adenomas in conjunction with neurological and psychiatric disorders and the tumor microenvironment.垂体腺瘤合并神经和精神疾病及肿瘤微环境的研究现状与展望
Front Neurosci. 2024 Apr 22;18:1294417. doi: 10.3389/fnins.2024.1294417. eCollection 2024.
2
Tumour microenvironment and pituitary tumour behaviour.肿瘤微环境与垂体肿瘤行为
J Endocrinol Invest. 2023 Jun;46(6):1047-1063. doi: 10.1007/s40618-023-02089-1. Epub 2023 Apr 15.
3
Up-regulation of the expressions of MiR-149-5p and MiR-99a-3p in exosome inhibits the progress of pituitary adenomas.
外泌体中MiR-149-5p和MiR-99a-3p表达上调可抑制垂体腺瘤进展。
Cell Biol Toxicol. 2021 Aug;37(4):633-651. doi: 10.1007/s10565-020-09570-0. Epub 2021 Jan 5.
4
SDF-1α/MicroRNA-134 Axis Regulates Nonfunctioning Pituitary Neuroendocrine Tumor Growth Targeting VEGFA.SDF-1α/miR-134 轴调控非功能性垂体神经内分泌肿瘤生长并靶向 VEGFA。
Front Endocrinol (Lausanne). 2020 Dec 9;11:566761. doi: 10.3389/fendo.2020.566761. eCollection 2020.
5
The role of the tumour microenvironment in the angiogenesis of pituitary tumours.肿瘤微环境在垂体肿瘤血管生成中的作用。
Endocrine. 2020 Dec;70(3):593-606. doi: 10.1007/s12020-020-02478-z. Epub 2020 Sep 18.
6
Experimental Evidence and Clinical Implications of Pituitary Adenoma Stem Cells.垂体腺瘤干细胞的实验证据和临床意义。
Front Endocrinol (Lausanne). 2020 Feb 20;11:54. doi: 10.3389/fendo.2020.00054. eCollection 2020.
7
Chemokines modulate the tumour microenvironment in pituitary neuroendocrine tumours.趋化因子调节垂体神经内分泌肿瘤的肿瘤微环境。
Acta Neuropathol Commun. 2019 Nov 8;7(1):172. doi: 10.1186/s40478-019-0830-3.
8
Survivin overexpression is potentially associated with pituitary adenoma invasiveness.存活素的过表达可能与垂体腺瘤的侵袭性有关。
Oncotarget. 2017 Nov 10;8(62):105637-105647. doi: 10.18632/oncotarget.22354. eCollection 2017 Dec 1.
9
A retrospective review of 34 cases of pediatric pituitary adenoma.对34例儿童垂体腺瘤的回顾性研究。
Childs Nerv Syst. 2017 Nov;33(11):1961-1967. doi: 10.1007/s00381-017-3538-3. Epub 2017 Jul 18.
10
Phenotypical and Pharmacological Characterization of Stem-Like Cells in Human Pituitary Adenomas.人垂体腺瘤中干细胞样细胞的表型和药理学特征。
Mol Neurobiol. 2017 Sep;54(7):4879-4895. doi: 10.1007/s12035-016-0025-x. Epub 2016 Aug 11.