• 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

CXCR1在不同乳腺组织中的表达特征及其表达与乳腺癌新辅助化疗疗效的相关性

Expression characteristic of CXCR1 in different breast tissues and the relevance between its expression and efficacy of neo-adjuvant chemotherapy in breast cancer.

作者信息

Xue Miao-Qun, Liu Jun, Sang Jian-Feng, Su Lei, Yao Yong-Zhong

机构信息

Department of General Surgery, Nanjing Drum Tower Hospital The Affiliated Hospital of Nanjing University Medical School, Nanjing 210008, China.

Department of General Surgery, The Jiang Bei People's Hospital of Nanjing, Nanjing 210048, China.

出版信息

Oncotarget. 2017 Jul 25;8(30):48930-48937. doi: 10.18632/oncotarget.16893.

DOI:10.18632/oncotarget.16893
PMID:28454081
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5564737/
Abstract

OBJECTIVE

To investigate chemokine receptor CXCR1 expression characteristic in different breast tissues and analyze the relationship between CXCR1 expression changes in breast cancer tissue and efficacy of neo-adjuvant chemotherapy.

RESULTS

Chemokine receptor CXCR1 was lowly expressed in normal breast tissues and breast fibroadenoma, but highly expressed in breast cancer. It was significantly correlated with pathological stage, tumor cell differentiation, and lymph node metastasis (P < 0.05). After neo-adjuvant chemotherapy, CXCR1 expression in breast cancer tissues decreased. Among these 104 breast cancer patients with different molecular subtypes, the survival rate with Luminal A was the highest, followed by the Luminal B breast cancer, TNBC was the worst.

MATERIALS AND METHODS

104 cases with breast carcinoma, 20 cases with normal breast and 20 cases with breast fibroadenoma were included and followed up. Immunohistochemistry was used to detect the expression of CXCR1 in the various tissues. The relationship between the CXCR1 expression changes in breast cancer biopsies and surgical specimens, as well as the efficacy of neo-adjuvant chemotherapy, was analyzed.

CONCLUSIONS

Chemokine receptor CXCR1 could be used as an indicator to predict benign or malignant breast disease, and it can even predict the malignancy degree of breast cancer, as well as its invasive ability and prognosis.

摘要

目的

探讨趋化因子受体CXCR1在不同乳腺组织中的表达特征,并分析乳腺癌组织中CXCR1表达变化与新辅助化疗疗效之间的关系。

结果

趋化因子受体CXCR1在正常乳腺组织和乳腺纤维瘤中低表达,而在乳腺癌中高表达。它与病理分期、肿瘤细胞分化及淋巴结转移显著相关(P<0.05)。新辅助化疗后,乳腺癌组织中CXCR1表达降低。在这104例不同分子亚型的乳腺癌患者中,Luminal A型的生存率最高,其次是Luminal B型乳腺癌,三阴性乳腺癌最差。

材料与方法

纳入104例乳腺癌患者、20例正常乳腺组织及20例乳腺纤维瘤患者并进行随访。采用免疫组织化学法检测各组织中CXCR1的表达。分析乳腺癌活检组织与手术标本中CXCR1表达变化以及新辅助化疗疗效之间的关系。

结论

趋化因子受体CXCR1可作为预测乳腺疾病良恶性的指标,甚至可预测乳腺癌的恶性程度、侵袭能力及预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ae/5564737/d20963ff8aab/oncotarget-08-48930-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ae/5564737/ea0d3bbdd14f/oncotarget-08-48930-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ae/5564737/35bff09ce769/oncotarget-08-48930-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ae/5564737/d20963ff8aab/oncotarget-08-48930-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ae/5564737/ea0d3bbdd14f/oncotarget-08-48930-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ae/5564737/35bff09ce769/oncotarget-08-48930-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ae/5564737/d20963ff8aab/oncotarget-08-48930-g003.jpg

相似文献

1
Expression characteristic of CXCR1 in different breast tissues and the relevance between its expression and efficacy of neo-adjuvant chemotherapy in breast cancer.CXCR1在不同乳腺组织中的表达特征及其表达与乳腺癌新辅助化疗疗效的相关性
Oncotarget. 2017 Jul 25;8(30):48930-48937. doi: 10.18632/oncotarget.16893.
2
Neutrophil expression of ICAM1, CXCR1, and VEGFR1 in patients with breast cancer before and after adjuvant chemotherapy.中性粒细胞 ICAM1、CXCR1 和 VEGFR1 的表达在乳腺癌患者辅助化疗前后的变化。
Anticancer Res. 2014 Sep;34(9):4693-9.
3
Relation Between Baseline CXCR1 Expression And Neoadjuvant Chemotherapy Response In Breast Cancer Patients.乳腺癌患者基线CXCR1表达与新辅助化疗反应之间的关系
J Pak Med Assoc. 2023 Apr;73(Suppl 4)(4):S52-S55. doi: 10.47391/JPMA.EGY-S4-8.
4
Clinical and pathological response to neoadjuvant chemotherapy based on primary tumor reduction is correlated to survival in hormone receptor-positive but not hormone receptor-negative locally advanced breast cancer.基于原发肿瘤缩小的新辅助化疗的临床和病理反应与激素受体阳性而非激素受体阴性的局部晚期乳腺癌的生存率相关。
Ann Surg Oncol. 2015 Jan;22(1):32-9. doi: 10.1245/s10434-014-3894-0. Epub 2014 Jul 11.
5
Prognostic value of Ki67 expression in HR-negative breast cancer before and after neoadjuvant chemotherapy.新辅助化疗前后Ki67表达在HR阴性乳腺癌中的预后价值
Int J Clin Exp Pathol. 2014 Sep 15;7(10):6862-70. eCollection 2014.
6
Nrdp1 expression to predict clinical outcome and efficacy of adjuvant anthracyclines-based chemotherapy in breast cancer: A retrospective study.Nrdp1表达对预测乳腺癌辅助蒽环类化疗的临床结局和疗效:一项回顾性研究。
Cancer Biomark. 2015;15(2):115-23. doi: 10.3233/CBM-140443.
7
Early response to neo-adjuvant chemotherapy in carcinoma of the breast predicts both successful breast-conserving surgery and decreased risk of ipsilateral breast tumor recurrence.早期对乳腺癌新辅助化疗的反应既可以预测保乳手术的成功,也可以降低同侧乳房肿瘤复发的风险。
Breast J. 2010 Jan-Feb;16(1):9-13. doi: 10.1111/j.1524-4741.2009.00864.x. Epub 2009 Nov 19.
8
Association of chemotactic factor receptor 5 gene with breast cancer.趋化因子受体5基因与乳腺癌的关联。
Genet Mol Res. 2013 Nov 7;12(4):5289-300. doi: 10.4238/2013.November.7.4.
9
FOXA1 expression after neoadjuvant chemotherapy is a prognostic marker in estrogen receptor-positive breast cancer.新辅助化疗后FOXA1的表达是雌激素受体阳性乳腺癌的一个预后标志物。
Breast Cancer. 2015 May;22(3):308-16. doi: 10.1007/s12282-013-0482-2. Epub 2013 Jun 16.
10
Sentinel lymph node biopsy after neoadjuvant chemotherapy in patients with cytologically proven node-positive breast cancer at diagnosis.诊断时细胞学证实淋巴结阳性的乳腺癌患者新辅助化疗后前哨淋巴结活检。
Ann Surg Oncol. 2013 Sep;20(9):2858-65. doi: 10.1245/s10434-013-2992-8. Epub 2013 May 5.

引用本文的文献

1
In vitro and in vivo evaluation of anti-tumorigenesis potential of nano silver for gastric cancer cells.体外和体内评估纳米银对胃癌细胞的抗肿瘤潜力。
J Mol Histol. 2024 Nov 29;56(1):14. doi: 10.1007/s10735-024-10315-0.
2
Clinical significance of the CXCL8/CXCR1/R2 signalling axis in patients with invasive breast cancer.CXCL8/CXCR1/R2信号轴在浸润性乳腺癌患者中的临床意义
Oncol Lett. 2024 Apr 10;27(6):260. doi: 10.3892/ol.2024.14393. eCollection 2024 Jun.
3
CXCR1: A Cancer Stem Cell Marker and Therapeutic Target in Solid Tumors.

本文引用的文献

1
Targeting CXCR1 on breast cancer stem cells: signaling pathways and clinical application modelling.靶向乳腺癌干细胞上的CXCR1:信号通路与临床应用建模
Oncotarget. 2015 Dec 22;6(41):43375-94. doi: 10.18632/oncotarget.6234.
2
CXCR7 mediates TGFβ1-promoted EMT and tumor-initiating features in lung cancer.CXCR7介导肺癌中转化生长因子β1(TGFβ1)促进的上皮-间质转化(EMT)和肿瘤起始特征。
Oncogene. 2016 Apr 21;35(16):2123-32. doi: 10.1038/onc.2015.274. Epub 2015 Jul 27.
3
Endothelial CXCR7 regulates breast cancer metastasis.内皮细胞CXCR7调节乳腺癌转移。
CXCR1:实体瘤中的一种癌症干细胞标志物及治疗靶点
Biomedicines. 2023 Feb 16;11(2):576. doi: 10.3390/biomedicines11020576.
4
Tackling Immune Targets for Breast Cancer: Beyond PD-1/PD-L1 Axis.攻克乳腺癌的免疫靶点:超越PD-1/PD-L1轴
Front Oncol. 2021 Mar 5;11:628138. doi: 10.3389/fonc.2021.628138. eCollection 2021.
5
Insights on CXC chemokine receptor 2 in breast cancer: An emerging target for oncotherapy.乳腺癌中CXC趋化因子受体2的研究进展:一种新兴的肿瘤治疗靶点
Oncol Lett. 2019 Dec;18(6):5699-5708. doi: 10.3892/ol.2019.10957. Epub 2019 Oct 3.
6
Chemokines Modulate Immune Surveillance in Tumorigenesis, Metastasis, and Response to Immunotherapy.趋化因子调节肿瘤发生、转移和免疫治疗反应中的免疫监视。
Front Immunol. 2019 Feb 27;10:333. doi: 10.3389/fimmu.2019.00333. eCollection 2019.
7
CAV2 promotes the growth of renal cell carcinoma through the EGFR/PI3K/Akt pathway.CAV2通过表皮生长因子受体/磷脂酰肌醇-3激酶/蛋白激酶B信号通路促进肾细胞癌的生长。
Onco Targets Ther. 2018 Sep 25;11:6209-6216. doi: 10.2147/OTT.S172803. eCollection 2018.
8
ALG3 Is Activated by Heat Shock Factor 2 and Promotes Breast Cancer Growth.ALG3 通过热休克因子 2 被激活并促进乳腺癌生长。
Med Sci Monit. 2018 May 25;24:3479-3487. doi: 10.12659/MSM.907461.
9
SPP1 promotes ovarian cancer progression via Integrin β1/FAK/AKT signaling pathway.分泌型磷酸蛋白1通过整合素β1/黏着斑激酶/蛋白激酶B信号通路促进卵巢癌进展。
Onco Targets Ther. 2018 Mar 12;11:1333-1343. doi: 10.2147/OTT.S154215. eCollection 2018.
Oncogene. 2016 Mar 31;35(13):1716-24. doi: 10.1038/onc.2015.236. Epub 2015 Jun 29.
4
Anchorage independency promoted tumor malignancy of melanoma cells under reattachment through elevated interleukin-8 and CXC chemokine receptor 1 expression.锚定非依赖性通过升高白细胞介素-8和CXC趋化因子受体1的表达促进了黑色素瘤细胞重新附着后的肿瘤恶性程度。
Melanoma Res. 2015 Feb;25(1):35-46. doi: 10.1097/CMR.0000000000000134.
5
Neutrophil expression of ICAM1, CXCR1, and VEGFR1 in patients with breast cancer before and after adjuvant chemotherapy.中性粒细胞 ICAM1、CXCR1 和 VEGFR1 的表达在乳腺癌患者辅助化疗前后的变化。
Anticancer Res. 2014 Sep;34(9):4693-9.
6
Targeting CXCR1/2 significantly reduces breast cancer stem cell activity and increases the efficacy of inhibiting HER2 via HER2-dependent and -independent mechanisms.靶向 CXCR1/2 可显著降低乳腺癌干细胞活性,并通过 HER2 依赖性和非依赖性机制增加抑制 HER2 的疗效。
Clin Cancer Res. 2013 Feb 1;19(3):643-56. doi: 10.1158/1078-0432.CCR-12-1063. Epub 2012 Nov 13.
7
CXCR1 as a novel target for directing reactive T cells toward melanoma: implications for adoptive cell transfer immunotherapy.CXCR1 作为一种新型靶点,可将反应性 T 细胞导向黑色素瘤:对过继细胞转移免疫治疗的影响。
Cancer Immunol Immunother. 2012 Oct;61(10):1833-47. doi: 10.1007/s00262-012-1245-1. Epub 2012 Mar 24.
8
Targeting CXCR1/CXCR2 receptor antagonism in malignant melanoma.靶向 CXCR1/CXCR2 受体拮抗作用治疗恶性黑色素瘤。
Expert Opin Ther Targets. 2010 Apr;14(4):435-42. doi: 10.1517/14728221003652471.
9
Differential activity of pro-angiogenic CXC chemokines.促血管生成 CXC 趋化因子的差异活性。
Microvasc Res. 2010 Jul;80(1):18-22. doi: 10.1016/j.mvr.2010.01.011. Epub 2010 Feb 6.
10
CXCR1 blockade selectively targets human breast cancer stem cells in vitro and in xenografts.CXCR1 阻断在体外和异种移植中选择性靶向人乳腺癌干细胞。
J Clin Invest. 2010 Feb;120(2):485-97. doi: 10.1172/JCI39397. Epub 2010 Jan 4.