Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P15088 (
mast cell
)
14,925
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Mastocytosis is a term used to denote a group of rare diseases characterized by an abnormal accumulation of neoplastic mast cells in various tissues and organs. In most patients with systemic mastocytosis, the neoplastic cells carry activating mutations in
KIT
Progress in mastocytosis research has long been hindered by the lack of suitable
in vitro
models, such as permanent human
mast cell
lines. In fact, only a few human
mast cell
lines are available to date: HMC-1,
LAD1
/2, LUVA, ROSA and MCPV-1. The HMC-1 and
LAD1
/2 cell lines were derived from patients with mast cell leukemia. By contrast, the more recently established LUVA, ROSA and MCPV-1 cell lines were derived from CD34
+
cells of non-mastocytosis donors. While some of these cell lines (
LAD1
/2, LUVA, ROSA
KIT WT
and MCPV-1) do not harbor
KIT
mutations, HMC-1 and ROSA
KIT D816V
cells exhibit activating
KIT
mutations found in mastocytosis and have thus been used to study disease pathogenesis. In addition, these cell lines are increasingly employed to validate new therapeutic targets and to screen for effects of new targeted drugs. Recently, the ROSA
KIT D816V
subclone has been successfully used to generate a unique
in vivo
model of advanced mastocytosis by injection into immunocompromised mice. Such a model may allow
in vivo
validation of data obtained
in vitro
with targeted drugs directed against mastocytosis. In this review, we discuss the major characteristics of all available human
mast cell
lines, with particular emphasis on the use of HMC-1 and ROSA
KIT D816V
cells in preclinical therapeutic research in mastocytosis.
...
PMID:Preclinical human models and emerging therapeutics for advanced systemic mastocytosis. 2997 35