| Literature DB >> 27622057 |
Cristina Ghirelli1, Benjamin Sadacca2, Fabien Reyal3, Raphaël Zollinger1, Paula Michea1, Philémon Sirven1, Lucia Pattarini1, Carolina Martínez-Cingolani1, Maude Guillot-Delost1, André Nicolas4, Alix Scholer-Dahirel1, Vassili Soumelis1.
Abstract
Thymic stromal lymphopoietin (TSLP) is an epithelial cell-derived cytokine that primes dendritic cells for Th2 induction. It has been implicated in different types of allergic diseases. Recent work suggested that TSLP could play an important role in the tumor microenvironment and influence tumor progression, in particular in breast cancer. In this study we systematically assessed the production of TSLP at the mRNA and protein levels in several human breast cancer cell lines, large-scale public transcriptomics data sets, and primary human breast tumors. We found that TSLP production was marginal, and concerned less than 10% of the tumors, with very low mRNA and protein levels. In most cases TSLP was undetectable and found to be expressed at lower levels in breast cancer as compared to normal breast tissue. Last, we could not detect any functional TSLP receptor (TSLPR) expression neither on hematopoietic cells nor on stromal cells within the primary tumor microenvironment. We conclude that TSLP-TSLPR pathway activity is not significantly detected within human breast cancer. Taken together, these observations do not support TSLP targeting in breast cancer.Entities:
Keywords: Breast cancer; cytokines; dendritic cells; thymic stromal lymphopoietin; tumor microenvironment
Year: 2016 PMID: 27622057 PMCID: PMC5007973 DOI: 10.1080/2162402X.2016.1178438
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110