Expression of angiogenic switch, cachexia and inflammation factors at the crossroad in undifferentiated thyroid carcinoma with BRAF(V600E)

Cancer Lett. 2016 Oct 1;380(2):577-585. doi: 10.1016/j.canlet.2015.07.012. Epub 2015 Jul 17.

Abstract

Cachexia is the result of complex metabolic alterations which cause morbidity and mortality in patients with advanced cancers including undifferentiated (anaplastic) thyroid carcinoma (ATC). ATC is a lethal disease with limited therapeutic options and unclear etiology for cachexia. We hypothesize that the BRAF(V600E) oncoprotein triggers microvascular endothelial cell tubule formation (in vitro angiogenesis) by means of factors which play a crucial role in angiogenic switch, inflammation/immune response and cachexia. We use human ATC cells and applied multiplex ELISA assay to screen for and measure angiogenic/cachectic and pro-inflammatory factors in the ATC-derived secretome. We find that vemurafenib anti-BRAF(V600E) therapy significantly reduces secreted VEGFA, VEGFC and IL6 protein levels compared to vehicle-treated ATC cells. As a result, the secretome from vemurafenib-treated ATC cells inhibits microvascular endothelial cell-related in vitro angiogenesis. Furthermore, ATC clinical samples express VEGFA, VEGFC and IL6 proteins. Our results suggest that angiogenic/cachectic and pro-inflammatory/immune response factors could play a crucial role in BRAF(V600E)-positive human ATC aggressiveness. Understanding the extent to which microenvironment-associated angiogenic factors participate in cachexia and cancer metabolism in advanced thyroid cancers will reveal new biomarkers and foster novel therapeutic approaches.

Keywords: Anaplastic thyroid cancer; Angiogenesis; BRAF(V600E); Cachexia; Cytokines; Inflammation.

MeSH terms

  • Angiogenic Proteins / metabolism*
  • Cachexia / enzymology*
  • Cachexia / genetics
  • Cell Line, Tumor
  • Cytokines / metabolism*
  • Humans
  • Indoles / pharmacology
  • Inflammation Mediators / metabolism*
  • Leptin / metabolism*
  • Mutation
  • Neovascularization, Pathologic*
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins B-raf / antagonists & inhibitors
  • Proto-Oncogene Proteins B-raf / genetics
  • Proto-Oncogene Proteins B-raf / metabolism*
  • Signal Transduction
  • Sulfonamides / pharmacology
  • Thyroid Carcinoma, Anaplastic / blood supply*
  • Thyroid Carcinoma, Anaplastic / drug therapy
  • Thyroid Carcinoma, Anaplastic / enzymology*
  • Thyroid Carcinoma, Anaplastic / genetics
  • Thyroid Neoplasms / blood supply*
  • Thyroid Neoplasms / drug therapy
  • Thyroid Neoplasms / enzymology*
  • Thyroid Neoplasms / genetics
  • Tumor Microenvironment
  • Vascular Endothelial Growth Factor A / metabolism
  • Vascular Endothelial Growth Factor C / metabolism
  • Vemurafenib

Substances

  • Angiogenic Proteins
  • Cytokines
  • Indoles
  • Inflammation Mediators
  • Leptin
  • Protein Kinase Inhibitors
  • Sulfonamides
  • VEGFA protein, human
  • VEGFC protein, human
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factor C
  • Vemurafenib
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf