دورية أكاديمية

Receptor for hyaluronic acid- mediated motility (RHAMM) regulates HT1080 fibrosarcoma cell proliferation via a β-catenin/c-myc signaling axis

التفاصيل البيبلوغرافية
العنوان: Receptor for hyaluronic acid- mediated motility (RHAMM) regulates HT1080 fibrosarcoma cell proliferation via a β-catenin/c-myc signaling axis
المؤلفون: Kouvidi, Katerina, Berdiaki, Aikaterini, Tzardi, Maria, KAROUSOU, EVGENIA, PASSI, ALBERTO, Nikitovic, Dragana, Tzanakakis, George N.
المساهمون: Kouvidi, Katerina, Berdiaki, Aikaterini, Tzardi, Maria, Karousou, Evgenia, Passi, Alberto, Nikitovic, Dragana, Tzanakakis, George N.
سنة النشر: 2016
المجموعة: IRInSubria - Institutional Repository Insubria (Università degli Studi dell’Insubria)
مصطلحات موضوعية: ERK1/2, Fibrosarcoma cell proliferation, LMWHA, RHAMM, β-Catenin, Active Transport, Cell Nucleu, Antigens, CD44, Cell Line, Tumor, Extracellular Matrix Protein, Fibrosarcoma, Human, Proto-Oncogene Proteins c-myc, beta Catenin, Cell Proliferation, Signal Transduction
الوصف: High levels of hyaluronan (HA) synthesis in various cancer tissues, including sarcomas, are correlated with tumorigenesis and malignant transformation. RHAMM (receptor for hyaluronic acid-mediated motility) is overexpressed during tumor development in different malignancies. β-Catenin is a crucial downstream mediator of the Wnt signaling cascade which facilitates carcinogenic events characterized by deregulated cell proliferation.
نوع الوثيقة: article in journal/newspaper
وصف الملف: STAMPA
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26825774; info:eu-repo/semantics/altIdentifier/wos/WOS:000371549000019; volume:1860; issue:4; firstpage:814-24; lastpage:824; numberofpages:11; journal:BIOCHIMICA ET BIOPHYSICA ACTA; http://hdl.handle.net/11383/2049143Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84969373529
DOI: 10.1016/j.bbagen.2016.01.019
الإتاحة: https://doi.org/10.1016/j.bbagen.2016.01.019Test
http://hdl.handle.net/11383/2049143Test
رقم الانضمام: edsbas.7984910B
قاعدة البيانات: BASE