• 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

初诊 ERBB2(HER2/neu)阳性乳腺癌患者的血清肿瘤坏死因子-α和白细胞介素-2浓度。

Serum tumor necrosis factor-alpha and interleukin-2 concentrations in newly diagnosed ERBB2 (HER2/neu) positive breast cancer patients.

机构信息

Department of Medical Oncology, Oncology Institute, Istanbul University, Istanbul, Turkey.

出版信息

Int J Biol Markers. 2009 Jul-Sep;24(3):142-6. doi: 10.1177/172460080902400303.

DOI:10.1177/172460080902400303
PMID:19787624
Abstract

AIM

Cytokines have been associated with symptoms and adverse outcomes in breast cancer. Overexpression of ERBB2 (c-erb-b2; formerly HER2/neu), which is a member of the epidermal growth receptor family, is associated with involvement of lymph nodes, large tumor size, high grade, steroid receptor negativity, aneuploidy, high proliferation rate, and low overall survival in breast cancer. The aim of the study was to examine whether ERBB2 amplification has any effect on circulating levels of tumor necrosis factor-alpha (TNF-alpha) and interleukin-2 (IL-2) in breast cancer patients.

MATERIAL AND METHODS

Fifty patients with primary breast carcinoma, classified as either ERBB2 (+) or (-) by the fluorescence in situ hybridization (FISH) technique, were included in the study. Cytokines were studied by ELISA according to the procedure described in the commercial kit.

RESULTS

IL-2 levels were found significantly higher in ERBB2+ patients than in controls (p<0.05). A significant negative correlation existed between ERBB2 positivity and estrogen receptor status (p=0.004). Plasma TNF-alpha and IL-2 levels were positively correlated in ERBB2+ breast cancer patients (p<0.01).

CONCLUSION

The increase in IL-2 concentrations observed in our study suggests an activation of T cells by ERBB2 peptides.

摘要

目的

细胞因子与乳腺癌的症状和不良预后有关。表皮生长因子受体家族成员 ERBB2(c-erb-b2;以前称为 HER2/neu)的过度表达与淋巴结受累、肿瘤体积大、高分级、甾体受体阴性、非整倍体、高增殖率和整体生存率低有关。本研究旨在探讨 ERBB2 扩增是否对乳腺癌患者循环肿瘤坏死因子-α(TNF-α)和白细胞介素-2(IL-2)水平有任何影响。

材料和方法

本研究纳入了 50 名原发性乳腺癌患者,通过荧光原位杂交(FISH)技术将其分类为 ERBB2(+)或(-)。根据商业试剂盒中描述的程序,通过 ELISA 研究细胞因子。

结果

与对照组相比,ERBB2+患者的 IL-2 水平显著升高(p<0.05)。ERBB2 阳性与雌激素受体状态呈显著负相关(p=0.004)。在 ERBB2+乳腺癌患者中,血浆 TNF-α和 IL-2 水平呈正相关(p<0.01)。

结论

我们的研究观察到 IL-2 浓度的增加提示 ERBB2 肽激活了 T 细胞。

相似文献

1
Serum tumor necrosis factor-alpha and interleukin-2 concentrations in newly diagnosed ERBB2 (HER2/neu) positive breast cancer patients.初诊 ERBB2(HER2/neu)阳性乳腺癌患者的血清肿瘤坏死因子-α和白细胞介素-2浓度。
Int J Biol Markers. 2009 Jul-Sep;24(3):142-6. doi: 10.1177/172460080902400303.
2
PGDS, a novel technique combining chromogenic in situ hybridization and immunohistochemistry for the assessment of ErbB2 (HER2/neu) status in breast cancer.PGDS,一种结合显色原位杂交和免疫组织化学用于评估乳腺癌中ErbB2(HER2/neu)状态的新技术。
Appl Immunohistochem Mol Morphol. 2007 Sep;15(3):316-24. doi: 10.1097/01.pai.0000213138.01536.2e.
3
IL-6, IL-8 and TNF-α levels correlate with disease stage in breast cancer patients.白细胞介素-6、白细胞介素-8和肿瘤坏死因子-α水平与乳腺癌患者的疾病分期相关。
Adv Clin Exp Med. 2017 May-Jun;26(3):421-426. doi: 10.17219/acem/62120.
4
Evaluation of HER2/neu oncoprotein in serum & tissue samples of women with breast cancer.乳腺癌女性血清和组织样本中HER2/neu癌蛋白的评估
Indian J Med Res. 2016 May;143(Supplement):S52-S58. doi: 10.4103/0971-5916.191769.
5
Influence of Circulating Tumour Cells on Production of IL-1α, IL-1β and IL-12 in Sera of Patients with Primary Diagnosis of Breast Cancer Before Treatment.循环肿瘤细胞对初诊乳腺癌患者治疗前血清中IL-1α、IL-1β和IL-12产生的影响。
Anticancer Res. 2016 Oct;36(10):5227-5236. doi: 10.21873/anticanres.11093.
6
Differential Gene Expression in Ductal Carcinoma In Situ of the Breast Based on ERBB2 Status.基于ERBB2状态的乳腺导管原位癌中的差异基因表达
Cancer Control. 2017 Jan;24(1):102-110. doi: 10.1177/107327481702400117.
7
Determination of HER2 status using both serum HER2 levels and circulating tumor cells in patients with recurrent breast cancer whose primary tumor was HER2 negative or of unknown HER2 status.在原发性肿瘤为HER2阴性或HER2状态未知的复发性乳腺癌患者中,利用血清HER2水平和循环肿瘤细胞来确定HER2状态。
Breast Cancer Res. 2007;9(5):R74. doi: 10.1186/bcr1783.
8
Increased TNF α, IL-6 and ErbB2 mRNA expression in peripheral blood leukocytes from breast cancer patients.乳腺癌患者外周血白细胞中肿瘤坏死因子α、白细胞介素-6和表皮生长因子受体2信使核糖核酸表达增加。
Med Oncol. 2014 Aug;31(8):38. doi: 10.1007/s12032-014-0038-0. Epub 2014 Jun 25.
9
The Neo-Bioscore Update for Staging Breast Cancer Treated With Neoadjuvant Chemotherapy: Incorporation of Prognostic Biologic Factors Into Staging After Treatment.新生物标志物更新在新辅助化疗治疗乳腺癌分期中的应用:治疗后预后生物因素在分期中的纳入。
JAMA Oncol. 2016 Jul 1;2(7):929-36. doi: 10.1001/jamaoncol.2015.6478.
10
Next-generation assessment of human epidermal growth factor receptor 2 gene (ERBB2) amplification status in invasive breast carcinoma: a focus on Group 4 by use of the 2018 American Society of Clinical Oncology/College of American Pathologists HER2 testing guideline.下一代人表皮生长因子受体 2 基因(ERBB2)在浸润性乳腺癌中扩增状态的评估:重点关注 2018 年美国临床肿瘤学会/美国病理学家学院 HER2 检测指南的第 4 组。
Histopathology. 2021 Mar;78(4):498-507. doi: 10.1111/his.14241. Epub 2020 Oct 12.

引用本文的文献

1
Identification of an acid sphingomyelinase ceramide kinase pathway in the regulation of the chemokine CCL5.鉴定酸鞘氨醇酶神经酰胺激酶通路在趋化因子 CCL5 调控中的作用。
J Lipid Res. 2018 Jul;59(7):1219-1229. doi: 10.1194/jlr.M084202. Epub 2018 May 3.
2
Pretreatment levels of circulating Th1 and Th2 cytokines, and their ratios, are associated with ER-negative and triple negative breast cancers.循环 Th1 和 Th2 细胞因子及其比值的预处理水平与 ER 阴性和三阴性乳腺癌相关。
Breast Cancer Res Treat. 2013 Jun;139(2):477-88. doi: 10.1007/s10549-013-2549-3. Epub 2013 Apr 30.
3
A different immunologic profile characterizes patients with HER-2-overexpressing and HER-2-negative locally advanced breast cancer: implications for immune-based therapies.
具有 HER-2 过表达和 HER-2 阴性局部晚期乳腺癌的患者具有不同的免疫表型:对免疫治疗的影响。
Breast Cancer Res. 2011;13(6):R117. doi: 10.1186/bcr3060.