نتایج جستجو برای: ژن fgfr2

تعداد نتایج: 17039  

Journal: :International journal of oncology 2010
Rieko Kawase Toshiyuki Ishiwata Yoko Matsuda Munehiko Onda Mitsuhiro Kudo Toshiyuki Takeshita Zenya Naito

Fibroblast growth factor receptors (FGFRs) 1-3 have IIIb and IIIc isoforms, and we reported that FGFR2 IIIb is highly expressed in cervical keratinizing squamous cell carcinoma (SCC). In this study, we determined the expression and roles of FGFR2 IIIc in cervical intraepithelial neoplasia (CIN) and cervical cancer. In CINs 1 and 2, FGFR2 IIIc was found to be localized at the basal to lower two-...

2013
Zamal Ahmed Chi-Chuan Lin Kin M. Suen Fernando A. Melo James A Levitt Klaus Suhling John E. Ladbury

Constitutive receptor tyrosine kinase phosphorylation requires regulation of kinase and phosphatase activity to prevent aberrant signal transduction. A dynamic mechanism is described here in which the adaptor protein, growth factor receptor-bound protein 2 (Grb2), controls fibroblast growth factor receptor 2 (FGFR2) signaling by regulating receptor kinase and SH2 domain-containing protein tyros...

Journal: :American journal of cancer research 2015
Zahra Timsah Jonathan Berrout Milind Suraokar Carmen Behrens Juhee Song J Jack Lee Cristina Ivan Mihai Gagea Michael Shires Xin Hu Courtney Vallien Charles V Kingsley IgnacioI Wistuba John E Ladbury

Lung adenocarcinoma is characterized by complex biology involving alterations at the genomic and protein expression levels. FGFR2 mutation and/or amplification are key drivers of disease progression and drug resistance in lung adenocarcinoma patients. These genetic alterations drive oncogenic downstream signalling due to the deregulated activity of the receptor. We have previously reported that...

Journal: :Cancer research 2012
Miao Guo Wei Liu Stefano Serra Sylvia L Asa Shereen Ezzat

Alternate splicing yields two distinct isoforms of the fibroblast growth factor (FGF) receptor FGFR2-IIIb and FGFR2-IIIc varying their extracellular structure in human thyroid cancer, in which FGFR expression is commonly dysregulated. In this study, we characterized the function of these variants in modulating thyroid cancer behavior. Enforced expression of either FGFR2-IIIb or FGFR2-IIIc in th...

Journal: :Cancer research 2008
Sara A Byron Michael G Gartside Candice L Wellens Mary A Mallon Jack B Keenan Matthew A Powell Paul J Goodfellow Pamela M Pollock

KRAS activation and PTEN inactivation are frequent events in endometrial tumorigenesis, occurring in 10% to 30% and 26% to 80% of endometrial cancers, respectively. Because we have recently shown activating mutations in fibroblast growth factor receptor 2 (FGFR2) in 16% of endometrioid endometrial cancers, we sought to determine the genetic context in which FGFR2 mutations occur. Analysis of 11...

2017
Tingting Huang Lei Wang Dian Liu Piao Li Huihua Xiong Liang Zhuang Li Sun Xianglin Yuan Hong Qiu

Fibroblast growth factor 7 (FGF7) is a mesenchyme-specific heparin-binding growth factor that binds FGF receptor 2 (FGFR2) to regulate numerous cellular and physiological processes. FGF7/FGFR2 signal is associated with gastric cancer progression. In the present study, we investigated the molecular mechanism by which FGF7/FGFR2 promotes invasion and migration in human gastric cancer. We first de...

2017
Haipeng Lei Chu-Xia Deng

Fibroblast growth factor receptor 2 (FGFR2) is a membrane-spanning tyrosine kinase that mediates signaling for FGFs. Recent studies detected various point mutations of FGFR2 in multiple types of cancers, including breast cancer, lung cancer, gastric cancer, uterine cancer and ovarian cancer, yet the casual relationship between these mutations and tumorigenesis is unclear. Here we will discuss p...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2017
E Van Cutsem Y-J Bang W Mansoor R D Petty Y Chao D Cunningham D R Ferry N R Smith P Frewer J Ratnayake P K Stockman E Kilgour D Landers

Background Approximately 5%-10% of gastric cancers have a fibroblast growth factor receptor-2 (FGFR2) gene amplification. AZD4547 is a selective FGFR-1, 2, 3 tyrosine kinase inhibitor with potent preclinical activity in FGFR2 amplified gastric adenocarcinoma SNU16 and SGC083 xenograft models. The randomized phase II SHINE study (NCT01457846) investigated whether AZD4547 improves clinical outcom...

Journal: :Molecular cancer therapeutics 2014
Seung Tae Kim Hye-Lim Jang Su Jin Lee Jeeyun Lee Yoon-La Choi Kyoung-Mee Kim Jeonghee Cho Se Hoon Park Young Suk Park Ho Yeong Lim Masakazu Yashiro Won Ki Kang Joon Oh Park

Pazopanib is an orally bioavailable, ATP-competitive, multitargeted tyrosine kinase inhibitor mainly targeting VEGFR2 and PDGFR tyrosine kinases, but the biologic sequences of pazopanib activities beyond antiangiogenesis are poorly defined. We used a panel of 38 gastric cancer cell lines to test the efficacy of pazopanib. In a growth inhibition assay, genomic changes indicated that pazopanib ha...

2015
Jinglin Zhang Dinesh Upadhya Lin Lu Lixing W. Reneker

Fibroblast growth factors (FGFs) play important roles in many aspects of embryonic development. During eye development, the lens and corneal epithelium are derived from the same surface ectodermal tissue. FGF receptor (FGFR)-signaling is essential for lens cell differentiation and survival, but its role in corneal development has not been fully investigated. In this study, we examined the corne...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید