دورية أكاديمية

Notch ligand Delta-like 1 promotes the metastasis of melanoma by enhancing tumor adhesion

التفاصيل البيبلوغرافية
العنوان: Notch ligand Delta-like 1 promotes the metastasis of melanoma by enhancing tumor adhesion
المؤلفون: J.P. Zhang, N. Li, W.Z. Bai, X.C. Qiu, B.A. Ma, Y. Zhou, Q.Y. Fan, L.Q. Shan
المصدر: Brazilian Journal of Medical and Biological Research, Vol 47, Iss 4, Pp 299-306 (2014)
بيانات النشر: Associação Brasileira de Divulgação Científica, 2014.
سنة النشر: 2014
المجموعة: LCC:Medicine (General)
LCC:Biology (General)
مصطلحات موضوعية: Delta-like 1, Notch signaling, Melanoma, Metastasis, Adhesion, N-cadherin, Medicine (General), R5-920, Biology (General), QH301-705.5
الوصف: Notch signaling plays a vital role in tumorigenicity and tumor progression by regulating proliferation, invasion, and the tumor microenvironment. Previous research by our group indicated that Notch ligand Delta-like 1 (Dll1) is involved in angiogenesis in melanoma, and we noticed that it took a longer time to trypsinize Dll1-expressing B16 melanoma cells than the control cells. In this article, we extended our study to investigate the effects of Dll1 on tumor cell adhesion and metastasis. Dll1 overexpression activated Notch signaling in B16 tumor cells and significantly enhanced the adhering capacity of B16 tumor cells both in vitro and in vivo. B16-Dll1 cells also had a higher metastatic potential than their counterpart in the mouse model of lung metastasis. Along with increased Dll1 expression, N-cadherin, but not E-cadherin, was upregulated in B16-Dll1 cells. These data suggested that Notch ligand Dll1 may enhance the adhesion and metastasis of melanoma cells by upregulation of N-cadherin.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1414-431X
Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2014000400299&lng=en&tlng=en; https://doaj.org/toc/1414-431X
DOI: 10.1590/1414-431X20143368
URL الوصول: https://doaj.org/article/1bc25d5fc2ec41bdad78c61784b04caa
رقم الأكسشن: edsdoj.1bc25d5fc2ec41bdad78c61784b04caa
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1414431X
DOI:10.1590/1414-431X20143368