Academic Journal

EMID1, a multifunctional molecule identified in a murine model for the invasion independent metastasis pathway

التفاصيل البيبلوغرافية
العنوان: EMID1, a multifunctional molecule identified in a murine model for the invasion independent metastasis pathway
المؤلفون: Takuya Kawata, Koji Muramatsu, Namiko Shishito, Naoki Ichikawa-Tomikawa, Takuma Oishi, Yuko Kakuda, Yasuto Akiyama, Ken Yamaguchi, Michiie Sakamoto, Takashi Sugino
المصدر: Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
بيانات النشر: Nature Portfolio, 2021.
سنة النشر: 2021
المجموعة: LCC:Medicine
LCC:Science
مصطلحات موضوعية: Medicine, Science
الوصف: Abstract EMI Domain Containing 1 (EMID1) was identified as a potential candidate metastasis-promoting gene. We sought to clarify the molecular function of EMID1 and the protein expression. Overexpression and knockdown studies using mouse tumor cell lines identified two novel functions of EMID1: intracellular signaling involving enhancement of cell growth via cell cycle promotion and suppression of cell motility, and inhibition of cell–matrix adhesion by extracellularly secreted EMID1. EMID1 deposited on the culture dish induced self-detachment of cells that overexpressed the protein and inhibited adhesion of additionally seeded cells. This multifunctional property involving both intracellular signaling and the extracellular matrix suggests that EMID1 may be a matricellular proteins. Expression analysis using immunohistochemical staining revealed expression of EMID1 that was limited to chief cells of the gastric fundic gland and β cells of the pancreatic islets in normal adult human tissues, implying cell-specific functions of this molecule. In addition, increased expression of EMID1 protein detected in some cases of human cancers implies that EMID1 might be a new therapeutic target for cancer treatment.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2045-2322
Relation: https://doaj.org/toc/2045-2322
DOI: 10.1038/s41598-021-96006-2
URL الوصول: https://doaj.org/article/1ce32b0292a04ddf90fc8ea5315239c5
رقم الانضمام: edsdoj.1ce32b0292a04ddf90fc8ea5315239c5
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20452322
DOI:10.1038/s41598-021-96006-2