4.7 Article

Cytokine and Chemokine Receptor Patterns of Human Malignant Melanoma Cell Lines

Journal

Publisher

MDPI
DOI: 10.3390/ijms23052644

Keywords

malignant melanoma; cytokine and chemokine receptor expression; invasion; BRAF mutation

Funding

  1. National Research Development and Innovation Fund [K 135752]
  2. European Regional Development Fund [GINOP 2.3.2 15 2016 00005]
  3. Hungarian Academy of Sciences [MTA11010, TK2016 78]
  4. New National Excellence Program of the Ministry for Innovation and Technology from the Source of National research, Development and Innovation Fund [UNKP-21-4-II-DE-361, UNKP-21-4-II-DE-136, UNKP-21-4-II-DE-363]

Ask authors/readers for more resources

This study investigated the gene expression patterns of cytokines and chemokine receptors in human melanoma cell lines. The results showed significant differential expression of these genes between cell lines originating from different subtypes of primary melanomas and those from melanoma metastases. The expression levels of certain receptor genes were positively correlated with invasive potential, while others were negatively correlated with BRAF(V600E) mutation.
Cytokine and chemokine receptors can promote tumor progression, invasion, and metastasis development by inducing different intracellular signaling pathways. The aim of this study was to determine the cytokine and chemokine receptor gene expression patterns in human melanoma cell lines. We found a large set of cytokine and chemokine receptor genes that were significantly differentially expressed between melanoma cell lines that originated from different subtypes of primary melanomas as well as cell lines that originated from melanoma metastases. The relative expressions of two receptor genes (CCR2 and TNFRSF11B) were positively correlated with the invasive potential of the cell lines, whereas a negative correlation was observed for the TNFRSF14 gene expression. We also found a small set of receptor genes that exhibited a significantly decreased expression in association with a BRAF(V600E) mutation. Based on our results, we assume that the analyzed cytokine and chemokine receptor collection may provide potential to distinguish the different subtypes of melanomas, helping us to understand the biological behavior of BRAF(V600E)-mutated melanoma cells.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available