نتایج جستجو برای: kit

تعداد نتایج: 29127  

Journal: :Blood 2001
R Chian S Young A Danilkovitch-Miagkova L Rönnstrand E Leonard P Ferrao L Ashman D Linnekin

Stem cell factor (SCF) binds the receptor tyrosine kinase c-Kit and is critical for normal hematopoiesis. Substitution of valine for aspartic acid 816 (D816V) constitutively actives human c-Kit, and this mutation is found in patients with mastocytosis, leukemia, and germ cell tumors. Immortalized murine progenitor cells (MIHCs) transduced with wild-type c-Kit proliferate in response to SCF, whe...

Journal: :Blood 1995
A M Turner L G Bennett N L Lin J Wypych T D Bartley R W Hunt H L Atkins K E Langley V Parker F Martin

Stem cell factor (SCF) triggers cell growth by binding to cell surface c-kit receptors. Soluble forms of several cytokine receptors have been described and may play a role in the modulation of cytokine activity in vivo. For these reasons, we investigated whether human hematopoietic cells produce soluble c-kit receptors. The human leukemia cell lines OCIM1 and MO7e display approximately 80,000 a...

Journal: :Blood 1994
T Tsujimura T Furitsu M Morimoto K Isozaki S Nomura Y Matsuzawa Y Kitamura Y Kanakura

The c-kit proto-oncogene encodes a receptor tyrosine kinase that is known to play a crucial role in hematopoiesis, especially in mast cell growth and differentiation. Although a number of dominant loss-of-function mutations of c-kit gene have been well characterized in mice, rats, and humans, little is known about the c-kit mutations contributing to ligand-independent activation of the c-kit re...

2016
Christian Posch Homayoun Moslehi Martina Sanlorenzo Gary Green Igor Vujic Renate Panzer-Grümayer Klemens Rappersberger Susana Ortiz-Urda

Mutations in the receptor tyrosine kinase c-KIT (KIT) are frequent oncogenic alterations in melanoma and are predominantly detected in tumors of acral, mucosal, and chronically sun-damaged skin. Research indicates that melanocytes with aberrant KIT signaling can be found in the distant periphery of the primary tumor; However, it is hitherto unknown whether KIT might confer a migratory advantage...

Journal: :The EMBO journal 1998
S Huang D Jean M Luca M A Tainsky M Bar-Eli

Expression of the tyrosine kinase receptor, c-KIT, progressively decreases during local tumor growth and invasion of human melanomas. We have previously shown that enforced c-KIT expression in highly metastatic cells inhibited tumor growth and metastasis in nude mice. Furthermore, the ligand for c-KIT, SCF, induces apoptosis in human melanoma cells expressing c-KIT under both in vitro and in vi...

2013
Zhongpu Chen Xiaodong Pan Yuyu Yao Fengdi Yan Long Chen Rong Huang Genshan Ma

BACKGROUND Cardiac progenitor cells (CPCs) have been proven suitable for stem cell therapy after myocardial infarction, especially c-kit(+)CPCs. CPCs marker c-kit and its ligand, the stem cell factor (SCF), are linked as c-kit/SCF axis, which is associated with the functions of proliferation and differentiation. In our previous study, we found that stromal cell-derived factor-1α (SDF-1α) could ...

2017
Wenjie Li Haiqian Xu Cheng Qian

BACKGROUND Adipose tissue-derived mesenchymal stem cells (ASCs) improve the regenerative ability and retention of fat grafts for breast reconstruction in cancer patients following mastectomy. However, ASCs have also been shown to promote breast cancer cell growth and metastasis. For the safety of ASC application, we aimed to identify specific markers for the subpopulation of ASCs that enhance t...

Journal: :Journal of immunology 2010
Keiko Maeda Chiharu Nishiyama Hideoki Ogawa Ko Okumura

The c-kit gene is expressed in hematopoietic stem cells and lineage progenitor cells but is downregulated during cell development in most lineages, except for mast cells. In mast cells, high expression of c-kit is maintained during development, and c-Kit signaling is essential for mast cell development. To analyze the mechanisms by which c-kit gene expression are regulated in mast cells, we exa...

2017
Yasushi Hara Yuuki Obata Keita Horikawa Yasutaka Tasaki Kyohei Suzuki Takatsugu Murata Isamu Shiina Ryo Abe

Gain-of-function mutations in Kit receptor tyrosine kinase result in the development of a variety of cancers, such as mast cell tumours, gastrointestinal stromal tumours (GISTs), acute myeloid leukemia, and melanomas. The drug imatinib, a selective inhibitor of Kit, is used for treatment of mutant Kit-positive cancers. However, mutations in the Kit kinase domain, which are frequently found in n...

2013
Misun Park Won Kyu Kim Meiying Song Minhee Park Hyunki Kim Hye Jin Nam Sung Hee Baek Hoguen Kim

Purpose: Abnormal signaling through receptor tyrosine kinase (RTK) moieties is important in tumorigenesis and drug targeting of colorectal cancers. Wild-type KIT (WT-KIT), a RTK that is activated upon bindingwith stemcell factor (SCF), is highly expressed in some colon cancers; however, little is knownabout the functional role of SCF-dependent KIT activation in colon cancer pathogenesis.We aime...

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