| Literature DB >> 31271515 |
Coralie Reger de Moura1,2, Maxime Battistella3,4,5, Anjum Sohail6, Anne Caudron1, Jean Paul Feugeas4,7,8, Marie-Pierre Podgorniak2, Cecile Pages9, Sarra Mazouz Dorval4,10, Oren Marco4,10, Suzanne Menashi11,12, Rafael Fridman6, Celeste Lebbé1,4,9, Samia Mourah1,2,4, Fanélie Jouenne1,2,4.
Abstract
The discoidin domain receptor 1 (DDR1) is a member of the receptor tyrosine kinase family that signals in response to collagen and that has been implicated in cancer progression. In the present study, we investigated the expression and role of DDR1 in human melanoma progression. Immunohistochemical staining of human melanoma specimens (n = 52) shows high DDR1 expression in melanoma lesions that correlates with poor prognosis. DDR1 expression was associated with the clinical characteristics of Clark level and ulceration and with BRAF mutations. Downregulation of DDR1 by small interfering RNA (siRNA) in vitro inhibited melanoma cells malignant properties, migration, invasion, and survival in several human melanoma cell lines. A DDR tyrosine kinase inhibitor (DDR1-IN-1) significantly inhibited melanoma cell proliferation in vitro, and ex vivo and in tumor xenografts, underlining the promising potential of DDR1 inhibition in melanoma.Entities:
Keywords: discoidin domain receptor 1; melanoma; prognosis; therapeutic target; tumor progression
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Year: 2019 PMID: 31271515 DOI: 10.1111/pcmr.12809
Source DB: PubMed Journal: Pigment Cell Melanoma Res ISSN: 1755-1471 Impact factor: 4.693