• 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

前哨淋巴结中 FOXP3+调节性 T 细胞密度高与胃癌下游非前哨淋巴结转移相关。

High FOXP3+ regulatory T-cell density in the sentinel lymph node is associated with downstream non-sentinel lymph-node metastasis in gastric cancer.

机构信息

Department of Pathology, Seoul National University Hospital, 28 Yeongon-dong, Jongno-gu, Seoul 110-744, Korea.

出版信息

Br J Cancer. 2011 Jul 26;105(3):413-9. doi: 10.1038/bjc.2011.248. Epub 2011 Jul 5.

DOI:10.1038/bjc.2011.248
PMID:21730981
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3172906/
Abstract

BACKGROUND

We aimed to evaluate the immunologic nature of sentinel lymph nodes (SLNs) in gastric cancer patients and to determine whether it can predict non-SLN metastasis.

METHODS

Sentinel lymph node samples were collected from 64 gastric carcinoma patients who had undergone gastrectomy with SLN biopsy. One representative SLN sample was selected from each patient and was subjected to immunostaining for CD8, CD57, FOXP3, and DC-LAMP. The numbers of marker-positive cells in each sample were counted. The relationships between various immune cell densities and clinicopathologic parameters or metastasis status of SLNs and non-SLNs were sought.

RESULTS

High FOXP3+ Treg density of the SLN was found to be significantly associated with the presence of metastasis in either SLNs or non-SLNs. DC-LAMP+ cell density of the SLN was the highest at the isolated tumours cell level, and this decreased along with an increase in tumour metastasis in either SLNs or non-SLNs. Univariate and multivariate logistic regression models revealed that high FOXP3+ Treg density of the SLN was an independently significant predictor of non-SLN metastasis.

CONCLUSIONS

This study is the first to indicate an important role of SLNs in metastatic dissemination of gastric cancer. Our findings suggest that Tregs could be a new therapeutic target for regulating the metastasis of gastric cancer.

摘要

背景

本研究旨在评估胃癌患者前哨淋巴结(SLN)的免疫学特性,并确定其是否可以预测非 SLN 转移。

方法

对 64 例行胃癌根治术和 SLN 活检的胃癌患者采集 SLN 样本。对每个患者的一个代表性 SLN 样本进行 CD8、CD57、FOXP3 和 DC-LAMP 的免疫染色。计数每个样本中标记阳性细胞的数量。寻找各种免疫细胞密度与 SLN 和非 SLN 的临床病理参数或转移状态之间的关系。

结果

发现 SLN 中高 FOXP3+Treg 密度与 SLN 或非 SLN 中的转移存在显著相关。SLN 的 DC-LAMP+细胞密度在孤立肿瘤细胞水平最高,随着 SLN 或非 SLN 中肿瘤转移的增加而降低。单因素和多因素逻辑回归模型表明,SLN 中高 FOXP3+Treg 密度是非 SLN 转移的独立显著预测因子。

结论

这项研究首次表明 SLN 在胃癌转移扩散中具有重要作用。我们的研究结果表明,Tregs 可能是调节胃癌转移的新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/3172906/a30f6ede7a11/bjc2011248f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/3172906/ca223fa1bea5/bjc2011248f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/3172906/ebf8ac6902f0/bjc2011248f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/3172906/a30f6ede7a11/bjc2011248f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/3172906/ca223fa1bea5/bjc2011248f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/3172906/ebf8ac6902f0/bjc2011248f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d75e/3172906/a30f6ede7a11/bjc2011248f3.jpg

相似文献

1
High FOXP3+ regulatory T-cell density in the sentinel lymph node is associated with downstream non-sentinel lymph-node metastasis in gastric cancer.前哨淋巴结中 FOXP3+调节性 T 细胞密度高与胃癌下游非前哨淋巴结转移相关。
Br J Cancer. 2011 Jul 26;105(3):413-9. doi: 10.1038/bjc.2011.248. Epub 2011 Jul 5.
2
Immune cell profile of sentinel lymph nodes in patients with malignant melanoma - FOXP3+ cell density in cases with positive sentinel node status is associated with unfavorable clinical outcome.黑色素瘤患者前哨淋巴结免疫细胞图谱 - 前哨淋巴结阳性病例中 FOXP3+ 细胞密度与不良临床结局相关。
J Transl Med. 2013 Feb 18;11:43. doi: 10.1186/1479-5876-11-43.
3
Sentinel lymph node mapping for 385 gastric cancer patients.385例胃癌患者的前哨淋巴结定位
J Surg Res. 2016 Jan;200(1):73-81. doi: 10.1016/j.jss.2015.06.064. Epub 2015 Jul 3.
4
Molecular analysis of melanoma-induced sentinel lymph node immune dysfunction.黑色素瘤诱导的前哨淋巴结免疫功能障碍的分子分析。
Cancer Immunol Immunother. 2011 May;60(5):685-92. doi: 10.1007/s00262-011-0982-x. Epub 2011 Feb 16.
5
Predicting Nonsentinel Lymph Node Metastasis in Breast Cancer: A Multicenter Retrospective Study.预测乳腺癌非前哨淋巴结转移:一项多中心回顾性研究。
J Surg Res. 2021 Aug;264:45-50. doi: 10.1016/j.jss.2021.01.047. Epub 2021 Mar 20.
6
Predictors of non-sentinel lymph node metastasis in breast cancer patients.乳腺癌患者非前哨淋巴结转移的预测因素
Eur J Cancer. 2004 Jul;40(11):1731-7. doi: 10.1016/j.ejca.2004.04.006.
7
[Clinical significance of sentinel lymph node detection by combining the dye-directed and radioguided methods in gastric cancer].[联合染料引导法与放射性引导法检测胃癌前哨淋巴结的临床意义]
Zhonghua Wai Ke Za Zhi. 2005 May 1;43(9):569-72.
8
Sentinel lymph node biopsy in gastric cancer: possible applications and limits.胃癌前哨淋巴结活检:可能的应用和局限性。
Eur J Surg Oncol. 2011 Jan;37(1):55-9. doi: 10.1016/j.ejso.2010.10.012. Epub 2010 Nov 27.
9
Maspin mRNA expression in sentinel lymph nodes predicts non-SLN metastasis in breast cancer patients with SLN metastasis.前哨淋巴结转移的乳腺癌患者中,前哨淋巴结中 maspin mRNA 的表达可预测非前哨淋巴结转移。
Histopathology. 2018 Dec;73(6):916-922. doi: 10.1111/his.13718. Epub 2018 Sep 25.
10
Size of Sentinel Node Metastasis Predicts Non-sentinel Node Involvement in Endometrial Cancer.前哨淋巴结转移灶大小可预测子宫内膜癌非前哨淋巴结受累情况。
Ann Surg Oncol. 2020 May;27(5):1589-1594. doi: 10.1245/s10434-019-08045-9. Epub 2019 Nov 4.

引用本文的文献

1
The clinical importance of the host anti-tumour reaction patterns in regional tumour draining lymph nodes in patients with locally advanced resectable gastric cancer: a systematic review and meta-analysis.局部进展期可切除胃癌患者区域肿瘤引流淋巴结中宿主抗肿瘤反应模式的临床重要性:系统评价和荟萃分析。
Gastric Cancer. 2023 Nov;26(6):847-862. doi: 10.1007/s10120-023-01426-w. Epub 2023 Sep 30.
2
Therapeutic strategies for gastric cancer targeting immune cells: Future directions.针对免疫细胞的胃癌治疗策略:未来方向。
Front Immunol. 2022 Sep 23;13:992762. doi: 10.3389/fimmu.2022.992762. eCollection 2022.
3
MiR-192-5p/RB1/NF-κBp65 signaling axis promotes IL-10 secretion during gastric cancer EMT to induce Treg cell differentiation in the tumour microenvironment.

本文引用的文献

1
Molecular diagnosis and translymphatic chemotherapy targeting sentinel lymph nodes of patients with early gastrointestinal cancers.针对早期胃肠道癌患者前哨淋巴结的分子诊断和经淋巴管化疗。
Digestion. 2010;82(3):187-91. doi: 10.1159/000309464. Epub 2010 Jun 25.
2
Distribution of Th17 cells and FoxP3(+) regulatory T cells in tumor-infiltrating lymphocytes, tumor-draining lymph nodes and peripheral blood lymphocytes in patients with gastric cancer.胃癌患者肿瘤浸润淋巴细胞、肿瘤引流淋巴结和外周血淋巴细胞中 Th17 细胞和 FoxP3(+)调节性 T 细胞的分布。
Cancer Sci. 2010 Sep;101(9):1947-54. doi: 10.1111/j.1349-7006.2010.01624.x.
3
miR-192-5p/RB1/NF-κBp65 信号轴在胃癌 EMT 期间促进 IL-10 分泌,从而诱导肿瘤微环境中的 Treg 细胞分化。
Clin Transl Med. 2022 Aug;12(8):e992. doi: 10.1002/ctm2.992.
4
Blood Stasis Syndrome Accelerates the Growth and Metastasis of Breast Cancer by Promoting Hypoxia and Immunosuppressive Microenvironment in Mice.血瘀证通过促进小鼠缺氧和免疫抑制微环境加速乳腺癌的生长和转移。
J Immunol Res. 2022 Jun 7;2022:7222638. doi: 10.1155/2022/7222638. eCollection 2022.
5
Correlation and prognostic implications of intratumor and tumor draining lymph node Foxp3 T regulatory cells in colorectal cancer.结直肠癌肿瘤内及引流淋巴结 Foxp3+T 调节细胞的相关性及其预后意义。
BMC Gastroenterol. 2022 Mar 16;22(1):122. doi: 10.1186/s12876-022-02205-0.
6
The Lymph Node Microenvironment May Invigorate Cancer Cells With Enhanced Metastatic Capacities.淋巴结微环境可能会激活具有更强转移能力的癌细胞。
Front Oncol. 2022 Feb 28;12:816506. doi: 10.3389/fonc.2022.816506. eCollection 2022.
7
Pretreatment CT-Based Radiomics Signature as a Potential Imaging Biomarker for Predicting the Expression of PD-L1 and CD8+TILs in ESCC.基于治疗前CT的影像组学特征作为预测食管鳞癌中PD-L1表达和CD8+肿瘤浸润淋巴细胞的潜在影像生物标志物
Onco Targets Ther. 2020 Nov 20;13:12003-12013. doi: 10.2147/OTT.S261068. eCollection 2020.
8
Metastatic Colonization: Escaping Immune Surveillance.转移定植:逃避免疫监视
Cancers (Basel). 2020 Nov 16;12(11):3385. doi: 10.3390/cancers12113385.
9
MicroRNA (miR) dysregulation during -induced gastric inflammation and cancer development: critical importance of miR-155.诱导性胃炎症和癌症发展过程中的微小RNA(miR)失调:miR-155的关键重要性
Oncotarget. 2020 Mar 10;11(10):894-904. doi: 10.18632/oncotarget.27520.
10
Immune crosstalk in cancer progression and metastatic spread: a complex conversation.肿瘤进展和转移扩散中的免疫串扰:一场复杂的对话。
Nat Rev Immunol. 2020 Aug;20(8):483-497. doi: 10.1038/s41577-019-0271-z. Epub 2020 Feb 5.
Low Foxp3 expression in negative sentinel lymph nodes is associated with node metastases in colorectal cancer.
前哨淋巴结阴性中低水平的Foxp3表达与结直肠癌的淋巴结转移相关。
Gut. 2010 Mar;59(3):419-20. doi: 10.1136/gut.2009.203422.
4
Significance of sentinel lymph node biopsy in malignant melanoma: overview of international data.前哨淋巴结活检在恶性黑色素瘤中的意义:国际数据概述。
Int J Clin Oncol. 2009 Dec;14(6):485-9. doi: 10.1007/s10147-009-0942-z. Epub 2009 Dec 5.
5
FOXP3 expression of micrometastasis-positive sentinel nodes in breast cancer patients.乳腺癌患者微转移阳性前哨淋巴结的FOXP3表达
Oncol Rep. 2009 Nov;22(5):1181-7. doi: 10.3892/or_00000553.
6
Simultaneous Foxp3 and IDO expression is associated with sentinel lymph node metastases in breast cancer.Foxp3和吲哚胺2,3-双加氧酶(IDO)的同时表达与乳腺癌前哨淋巴结转移相关。
BMC Cancer. 2009 Jul 15;9:231. doi: 10.1186/1471-2407-9-231.
7
Limited gastrectomy with dissection of sentinel node stations for early gastric cancer with negative sentinel node biopsy.前哨淋巴结活检阴性的早期胃癌行有限胃切除术并清扫前哨淋巴结站
Ann Surg. 2009 Jun;249(6):942-7. doi: 10.1097/SLA.0b013e3181a77e7e.
8
Accumulation of regulatory T cells in sentinel lymph nodes is a prognostic predictor in patients with node-negative breast cancer.前哨淋巴结中调节性T细胞的积聚是淋巴结阴性乳腺癌患者的预后预测指标。
Eur J Cancer. 2009 Aug;45(12):2123-31. doi: 10.1016/j.ejca.2009.03.024. Epub 2009 Apr 22.
9
Factors associated with detection failure and false-negative sentinel node biopsy findings in gastric cancer: results of prospective single center trials.胃癌前哨淋巴结活检检测失败及假阴性结果的相关因素:前瞻性单中心试验结果
J Surg Oncol. 2009 Mar 1;99(3):137-42. doi: 10.1002/jso.21222.
10
The evolution of lymph node assessment in breast cancer.乳腺癌中淋巴结评估的演变
J Surg Oncol. 2009 Mar 15;99(4):194-8. doi: 10.1002/jso.21201.