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Signal transduction via the stem cell factor receptor/c-Kit.

Rönnstrand, Lars LU orcid (2004) In Cellular and Molecular Life Sciences 61(19-20). p.2535-2548
Abstract
Together with its ligand, stem cell factor, the receptor tyrosine kinase c-Kit is a key controlling receptor for a number of cell types, including hematopoietic stem cells, mast cells, melanocytes and germ cells. Gain-of-function mutations in c-Kit have been described in a number of human cancers, including testicular germinomas, acute myeloid leukemia and gastrointestinal stromal tumors.

Stimulation of c-Kit by its ligand leads to dimerization of receptors, activation of its intrinsic tyrosine kinase activity and phosphorylation of key tyrosine residues within the receptor. These phosphorylated tyrosine residues serve as docking sites for a number of signal transduction molecules containing Src homology 2 domains, which will... (More)
Together with its ligand, stem cell factor, the receptor tyrosine kinase c-Kit is a key controlling receptor for a number of cell types, including hematopoietic stem cells, mast cells, melanocytes and germ cells. Gain-of-function mutations in c-Kit have been described in a number of human cancers, including testicular germinomas, acute myeloid leukemia and gastrointestinal stromal tumors.

Stimulation of c-Kit by its ligand leads to dimerization of receptors, activation of its intrinsic tyrosine kinase activity and phosphorylation of key tyrosine residues within the receptor. These phosphorylated tyrosine residues serve as docking sites for a number of signal transduction molecules containing Src homology 2 domains, which will thereby be recruited to the receptor and activated many times through phosphorylation by the receptor. This review discusses our current knowledge of signal transduction molecules and signal transduction pathways activated by c-Kit and how their activation can be connected to the physiological outcome of c-Kit signaling. (Less)
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author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Cellular and Molecular Life Sciences
volume
61
issue
19-20
pages
2535 - 2548
publisher
Birkhäuser Verlag
external identifiers
  • wos:000224888600012
  • scopus:9744246909
ISSN
1420-9071
DOI
10.1007/s00018-004-4189-6
language
English
LU publication?
yes
additional info
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Experimental Clinical Chemistry (013016010)
id
efc8642d-c784-4124-960c-8e79d10813ad (old id 130962)
date added to LUP
2016-04-01 16:37:27
date last changed
2022-04-22 23:23:28
@article{efc8642d-c784-4124-960c-8e79d10813ad,
  abstract     = {{Together with its ligand, stem cell factor, the receptor tyrosine kinase c-Kit is a key controlling receptor for a number of cell types, including hematopoietic stem cells, mast cells, melanocytes and germ cells. Gain-of-function mutations in c-Kit have been described in a number of human cancers, including testicular germinomas, acute myeloid leukemia and gastrointestinal stromal tumors.<br/><br>
Stimulation of c-Kit by its ligand leads to dimerization of receptors, activation of its intrinsic tyrosine kinase activity and phosphorylation of key tyrosine residues within the receptor. These phosphorylated tyrosine residues serve as docking sites for a number of signal transduction molecules containing Src homology 2 domains, which will thereby be recruited to the receptor and activated many times through phosphorylation by the receptor. This review discusses our current knowledge of signal transduction molecules and signal transduction pathways activated by c-Kit and how their activation can be connected to the physiological outcome of c-Kit signaling.}},
  author       = {{Rönnstrand, Lars}},
  issn         = {{1420-9071}},
  language     = {{eng}},
  number       = {{19-20}},
  pages        = {{2535--2548}},
  publisher    = {{Birkhäuser Verlag}},
  series       = {{Cellular and Molecular Life Sciences}},
  title        = {{Signal transduction via the stem cell factor receptor/c-Kit.}},
  url          = {{http://dx.doi.org/10.1007/s00018-004-4189-6}},
  doi          = {{10.1007/s00018-004-4189-6}},
  volume       = {{61}},
  year         = {{2004}},
}