4.5 Article

Expression of the inflammatory chemokines CCL2, CCL5 and CXCL2 and the receptors CCR1-3 and CXCR2 in T lymphocytes from mammary tumor-bearing mice

Journal

CELLULAR IMMUNOLOGY
Volume 270, Issue 2, Pages 172-182

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.cellimm.2011.05.004

Keywords

Chemokines; Chemokine receptors; T lymphocytes; Mammary tumor; Angiogenesis

Funding

  1. Florida division of the American Cancer Society [F02S-FAU-1]
  2. NIH [R15 CA135513-01, R15 CA135513-01-OS1]
  3. NATIONAL CANCER INSTITUTE [R15CA135513] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [F32AI056963] Funding Source: NIH RePORTER

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Chemokines and their receptors have been studied in several solid tumor models as mediators of inflammation. In turn, inflammation has been implicated in the promotion and progression of tumors, and as such, chemokines have been proposed as novel molecular targets for chemotherapy. While the expression of these molecules has been described in tumor cells, endothelial cells, macrophages and neutrophils, less attention has been paid to the expression profile of these molecules by T lymphocytes in the periphery or infiltrating the tumor. Using the D1 -DMBA-3 murine mammary adenocarcinoma model, we aimed to better characterize the differential expression of chemokines and/or their receptors in the host and in the tumor microenvironment, and specifically, in the T cells of tumor-bearing mice compared to normal control animals. We found that T lymphocytes from tumor-bearing mice express the pro-inflammatory chemokines, CCL2, CCL5 and CXCL2, as well as the chemokine receptors, CCR1, CCR2,CCR3 and CXCR2. (C) 2011 Elsevier Inc. All rights reserved.

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