Gene expression analyses of primary melanomas reveal CTHRC1 as an important player in melanoma progression

Autor: Susanna Virolainen, Pirjo Laakkonen, Vadim Le Joncour, Erkki Hölttä, Olli Saksela, Tiina Jahkola, Johanna Eriksson, Pirjo Nummela
Rok vydání: 2016
Předmět:
0301 basic medicine
Pathology
Skin Neoplasms
Angiogenesis
Apoptosis
Metastasis
Mice
0302 clinical medicine
Cell Movement
Tumor Cells
Cultured

Extracellular Matrix Proteins
Mice
Inbred BALB C

Gene knockdown
Melanoma
invasion/metastasis
Integrin beta3
NFATC2
Cell migration
Prognosis
Metastatic breast cancer
humanities
3. Good health
Gene Expression Regulation
Neoplastic

Oncology
030220 oncology & carcinogenesis
Disease Progression
Melanocytes
Female
Research Paper
medicine.medical_specialty
Mice
Nude

TGFβ
03 medical and health sciences
TGF beta signaling pathway
melanoma
Biomarkers
Tumor

Cell Adhesion
medicine
Animals
Humans
neoplasms
Cell Proliferation
Neoplasm Staging
NFATC Transcription Factors
business.industry
Gene Expression Profiling
medicine.disease
Xenograft Model Antitumor Assays
Fibronectins
Gene expression profiling
030104 developmental biology
Cancer research
Stromal Cells
business
CTHRC1
Zdroj: Oncotarget
ISSN: 1949-2553
DOI: 10.18632/oncotarget.7604
Popis: // Johanna Eriksson 1 , Vadim Le Joncour 2 , Pirjo Nummela 1 , Tiina Jahkola 3 , Susanna Virolainen 1 , Pirjo Laakkonen 2 , Olli Saksela 4 , Erkki Holtta 1 1 Department of Pathology, University of Helsinki, FI-00014 Helsinki, Finland 2 University of Helsinki, Research Programs Unit, Translational Cancer Biology, Biomedicum Helsinki, FI-00014 Helsinki, Finland 3 Department of Plastic Surgery, Helsinki University Central Hospital, FI-00029 Helsinki, Finland 4 Department of Dermatology, Helsinki University Central Hospital, FI-00029 Helsinki, Finland Correspondence to: Erkki Holtta, e-mail: erkki.holtta@helsinki.fi Keywords: melanoma, invasion/metastasis, CTHRC1, NFATC2, TGFβ Received: June 11, 2015 Accepted: January 31, 2016 Published: February 23, 2016 ABSTRACT Melanoma is notorious for its high tendency to metastasize and its refractoriness to conventional treatments after metastasis, and the responses to most targeted therapies are short-lived. A better understanding of the molecular mechanisms behind melanoma development and progression is needed to develop more effective therapies and to identify new markers to predict disease behavior. Here, we compared the gene expression profiles of benign nevi, and non-metastatic and metastatic primary melanomas to identify any common changes in disease progression. We identified several genes associated with inflammation, angiogenesis, and extracellular matrix modification to be upregulated in metastatic melanomas. We selected one of these genes, collagen triple helix repeat containing 1 ( CTHRC1 ), for detailed analysis, and found that CTHRC1 was expressed in both melanoma cells and the associated fibroblasts, as well as in the endothelium of tumor blood vessels. Knockdown of CTHRC1 expression by shRNAs in melanoma cells inhibited their migration in Transwell assays and their invasion in three-dimensional collagen and Matrigel matrices. We also elucidated the possible down-stream effectors of CTHRC1 by gene expression profiling of the CTHRC1-knockdown cells. Our analyses showed that CTHRC1 is regulated coordinately with fibronectin and integrin β3 by the pro-invasive and -angiogenic transcription factor NFATC2. We also found CTHRC1 to be a target of TFGβ and BRAF. These data highlight the importance of tumor stroma in melanoma progression. Furthermore, CTHRC1 was recognized as an important mediator of melanoma cell migration and invasion, providing together with its regulators—NFATC2, TGFβ, and BRAF—attractive therapeutic targets against metastatic melanomas.
Databáze: OpenAIRE