Literature DB >> 20598333

Chemokine receptor CXCR4 overexpression predicts recurrence for hormone receptor-positive, node-negative breast cancer patients.

Quyen D Chu1, Neal T Holm, Prince Madumere, Lester W Johnson, Fleurette Abreo, Benjamin D L Li.   

Abstract

BACKGROUND: The expected outcome for hormone receptor-positive, node-negative patients should be favorable. However, some patients do develop metastatic disease and the mechanism for this observation is poorly understood. CXCR4 is a chemokine receptor that has been implicated to play a pivotal role in breast cancer growth and metastasis. Its predictive role has not been fully evaluated. We determined to see whether CXCR4 can predict outcome in this subset of patients.
METHODS: We accrued and analyzed data from 101 patients with hormone receptor-positive, node-negative breast cancers. The CXCR4 level was detected using Western blots and its level was defined as either low (<6.6-fold) or high (≥6.6-fold). Primary end points were systemic cancer recurrence and death. Statistical analysis performed included Spearman's correlation, Kaplan-Meier survival analysis, and Cox proportional hazard model.
RESULTS: Although benign breast tissues had an undetectable level of CXCR4, all 101 cancer specimens had overexpressed CXCR4 (mean 6.4 ± 3.4-fold). There were 79 patients in the low CXCR4 group and 22 patients in the high CXCR4 group. High CXCR4 overexpression was predictive of both cancer recurrence (P = .002) and overall survival (P = .0012).
CONCLUSION: High CXCR4 overexpression in primary tumors was predictive of worse outcomes in hormone receptor-positive, node-negative breast cancer patients. Copyright Â
© 2011 Mosby, Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 20598333     DOI: 10.1016/j.surg.2010.05.016

Source DB:  PubMed          Journal:  Surgery        ISSN: 0039-6060            Impact factor:   3.982


  10 in total

1.  Bone morphogenetic protein 4 (BMP4) is required for migration and invasion of breast cancer.

Authors:  Dan Guo; Jiayi Huang; Jianping Gong
Journal:  Mol Cell Biochem       Date:  2011-12-14       Impact factor: 3.396

2.  Potential of CXCR4/CXCL12 Chemokine Axis in Cancer Drug Delivery.

Authors:  Yan Wang; Ying Xie; David Oupický
Journal:  Curr Pharmacol Rep       Date:  2016-01-04

3.  Balancing polymer hydrophobicity for ligand presentation and siRNA delivery in dual function CXCR4 inhibiting polyplexes.

Authors:  Y Wang; J Li; Y Chen; D Oupický
Journal:  Biomater Sci       Date:  2015-07       Impact factor: 6.843

4.  Effect of biodegradability on CXCR4 antagonism, transfection efficacy and antimetastatic activity of polymeric Plerixafor.

Authors:  Jing Li; David Oupický
Journal:  Biomaterials       Date:  2014-04-13       Impact factor: 12.479

5.  TP53 mutation, epithelial-mesenchymal transition, and stemlike features in breast cancer subtypes.

Authors:  Danila Coradini; Marco Fornili; Federico Ambrogi; Patrizia Boracchi; Elia Biganzoli
Journal:  J Biomed Biotechnol       Date:  2012-07-30

6.  Use of a single hybrid imaging agent for integration of target validation with in vivo and ex vivo imaging of mouse tumor lesions resembling human DCIS.

Authors:  Tessa Buckle; Joeri Kuil; Nynke S van den Berg; Anton Bunschoten; Hildo J Lamb; Hushan Yuan; Lee Josephson; Jos Jonkers; Alexander D Borowsky; Fijs W B van Leeuwen
Journal:  PLoS One       Date:  2013-01-11       Impact factor: 3.240

Review 7.  CXCR4 over-expression and survival in cancer: a system review and meta-analysis.

Authors:  Hongli Zhao; Liyuan Guo; Hong Zhao; Jiaxin Zhao; Hao Weng; Bin Zhao
Journal:  Oncotarget       Date:  2015-03-10

8.  Chemokine (C-X-C motif) receptor 4 RNA interference inhibits bone metastasis in breast cancer.

Authors:  Heng Zeng; Wei Wei; Xiaotao Xu
Journal:  Oncol Lett       Date:  2014-04-28       Impact factor: 2.967

Review 9.  Expression of CXCR4 and breast cancer prognosis: a systematic review and meta-analysis.

Authors:  Zhigang Zhang; Chao Ni; Wuzhen Chen; Ping Wu; Zhen Wang; Junhua Yin; Jian Huang; Fuming Qiu
Journal:  BMC Cancer       Date:  2014-01-29       Impact factor: 4.430

10.  CXCR4 antagonism in combination with IDO1 inhibition weakens immune suppression and inhibits tumor growth in mouse breast cancer bone metastases.

Authors:  Jian Zhang; Yanxia Pang; Tao Xie; Liulong Zhu
Journal:  Onco Targets Ther       Date:  2019-06-28       Impact factor: 4.147

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.