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No evidence for TSLP pathway activity in human breast cancer
- Source :
- OncoImmunology, OncoImmunology, Taylor & Francis, 2016, 5 (8), pp.1-32. ⟨10.1080/2162402X.2016.1178438⟩, OncoImmunology, 2016, 5 (8), pp.1-32. ⟨10.1080/2162402X.2016.1178438⟩
- Publication Year :
- 2016
- Publisher :
- Taylor & Francis, 2016.
-
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.
- Subjects :
- 0301 basic medicine
Stromal cell
Thymic stromal lymphopoietin
medicine.medical_treatment
[SDV]Life Sciences [q-bio]
Immunology
Biology
03 medical and health sciences
Breast cancer
thymic stromal lymphopoietin
medicine
Immunology and Allergy
tumor microenvironment
dendritic cells
Original Research
Tumor microenvironment
Cancer
medicine.disease
Primary tumor
cytokines
3. Good health
030104 developmental biology
Cytokine
Oncology
Tumor progression
Subjects
Details
- Language :
- English
- ISSN :
- 21624011 and 2162402X
- Database :
- OpenAIRE
- Journal :
- OncoImmunology, OncoImmunology, Taylor & Francis, 2016, 5 (8), pp.1-32. ⟨10.1080/2162402X.2016.1178438⟩, OncoImmunology, 2016, 5 (8), pp.1-32. ⟨10.1080/2162402X.2016.1178438⟩
- Accession number :
- edsair.doi.dedup.....aa7385a59ada6ce30c650c36ada0a9db
- Full Text :
- https://doi.org/10.1080/2162402X.2016.1178438⟩