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趋化因子在乳腺癌病理学中的作用及其作为治疗靶点的可能用途。

The role of chemokines in breast cancer pathology and its possible use as therapeutic targets.

机构信息

Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, A.P. 70228, 04510 México, DF, Mexico.

Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, A.P. 70228, 04510 México, DF, Mexico ; Dirección de Enfermedades Crónicas y Cáncer, Centro de Investigación Sobre Enfermedades Infecciosas, Instituto Nacional de Salud Pública, 62115 Cuernavaca, MOR, Mexico.

出版信息

J Immunol Res. 2014;2014:849720. doi: 10.1155/2014/849720. Epub 2014 Aug 5.


DOI:10.1155/2014/849720
PMID:25165728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4139084/
Abstract

Chemokines are small proteins that primarily regulate the traffic of leukocytes under homeostatic conditions and during specific immune responses. The chemokine-chemokine receptor system comprises almost 50 chemokines and approximately 20 chemokine receptors; thus, there is no unique ligand for each receptor and the binding of different chemokines to the same receptor might have disparate effects. Complicating the system further, these effects depend on the cellular milieu. In cancer, although chemokines are associated primarily with the generation of a protumoral microenvironment and organ-directed metastasis, they also mediate other phenomena related to disease progression, such as angiogenesis and even chemoresistance. Therefore, the chemokine system is becoming a target in cancer therapeutics. We review the emerging data and correlations between chemokines/chemokine receptors and breast cancer, their implications in cancer progression, and possible therapeutic strategies that exploit the chemokine system.

摘要

趋化因子是一类小分子蛋白,主要在稳态条件下和特定免疫应答过程中调节白细胞的迁移。趋化因子-趋化因子受体系统包含近 50 种趋化因子和大约 20 种趋化因子受体;因此,没有一种趋化因子可以特异性地与某一受体结合,而不同的趋化因子与同一受体的结合可能会产生不同的效应。使情况更为复杂的是,这些效应取决于细胞微环境。在癌症中,尽管趋化因子主要与肿瘤微环境的产生和器官定向转移有关,但它们也介导与疾病进展相关的其他现象,如血管生成,甚至是化疗耐药。因此,趋化因子系统正成为癌症治疗的一个靶点。我们综述了趋化因子/趋化因子受体与乳腺癌之间的新出现的数据和关联,以及它们在癌症进展中的意义,以及利用趋化因子系统的可能治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeb8/4139084/8593ab33d384/JIR2014-849720.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeb8/4139084/7fcd37673c6e/JIR2014-849720.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeb8/4139084/8593ab33d384/JIR2014-849720.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeb8/4139084/7fcd37673c6e/JIR2014-849720.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeb8/4139084/8593ab33d384/JIR2014-849720.002.jpg

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[1]
The role of chemokines in breast cancer pathology and its possible use as therapeutic targets.

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[7]
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[8]
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[9]
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[10]
CXCR6-CXCL16 Axis Promotes Breast Cancer by Inducing Oncogenic Signaling.

Cancers (Basel). 2021-7-16

本文引用的文献

[1]
Targeting CXCL12/CXCR4 signaling with oncolytic virotherapy disrupts tumor vasculature and inhibits breast cancer metastases.

Proc Natl Acad Sci U S A. 2013-3-18

[2]
CCL20 induces migration and proliferation on breast epithelial cells.

J Cell Physiol. 2013-9

[3]
The Role of chemokine receptor CXCR4 in breast cancer metastasis.

Am J Cancer Res. 2013-1-18

[4]
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Curr Mol Med. 2013-3

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The depletion of interleukin-8 causes cell cycle arrest and increases the efficacy of docetaxel in breast cancer cells.

Biochem Biophys Res Commun. 2013-1-12

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Clin Cancer Res. 2012-11-13

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Clin Cancer Res. 2012-8-29

[8]
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Breast Cancer Res Treat. 2012-8-22

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Cell. 2012-7-6

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Cancer Res. 2012-5-25

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