Literature DB >> 25120788

Transcription factors related to epithelial mesenchymal transition in tumor center and margin in invasive lung adenocarcinoma.

Young-In Maeng1, Kyung-Hyun Kim1, Jung-Yeon Kim1, Sun-Jae Lee1, Woo-Jung Sung1, Chong-Kee Lee2, Jae-Bok Park1, Kwan-Kyu Park1.   

Abstract

The tumor microenvironment has many roles involving tumor progression, invasion and metastasis. The tumor cells at the tumor border loose epithelial properties and acquire mesenchymal features. This, epithelial-to-mesenchymal transition (EMT) has been suggested to be an important process for tissue and lymphovascular invasion. Pulmonary tissue samples from 15 patients with primary adenocarcinoma were evaluated with using immunofluorescence multi-staining the EMT-associated markers including E-cadherin and alpha-smooth muscle actin (α-SMA), and transcription factors including E-SNAIL and SLUG, and ZEB1. The data were analyzed in specific area, such as tumor center and tumor border. In this study we show that the invasive adenocarcinoma differentially expressed SNAIL and SLUG, and Zeb1 and it was associated with the loss of epithelial marker (E-cadherin) and gaining of mesenchymal marker (α-SMA) at the invasive border of lung carcinoma. The positive rates of SNAIL and ZEB1 were 26.7% and 0% in the tumor center and 40% and 20% in tumor margin, respectively. In addition, the expression of both SNAIL and ZEB1 at the border of tumor was observed in two cases (2/10). These two cases were associated with lymph node metastasis and advanced stage. The process of EMT has been suggested to be of prime importance for tissue and lymphovascular invasion. The process of EMT may be activated in the tumor border of lung adenocarcinoma. Related transcription factors, such as SNAIL and SLUG, and ZEB1, might be induced by paracrine effects of surrounded inflammatory cells and fibroblasts.

Entities:  

Keywords:  Epithelial mesenchymal transition; SLUG; SNAIL; ZEB1; lung adenocarcinoma

Mesh:

Substances:

Year:  2014        PMID: 25120788      PMCID: PMC4129023     

Source DB:  PubMed          Journal:  Int J Clin Exp Pathol        ISSN: 1936-2625


  38 in total

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  5 in total

1.  Microenvironmental interactions and expression of molecular markers associated with epithelial-to-mesenchymal transition in colorectal carcinoma.

Authors:  Sun-Jae Lee; Chun-Seok Yang; Dae-Dong Kim; Yu-Na Kang; Sang Gyu Kwak; Jae-Bok Park; Chang-Ho Cho; Kwan-Kyu Park
Journal:  Int J Clin Exp Pathol       Date:  2015-11-01

2.  Conditioned media from human ovarian cancer endothelial progenitor cells induces ovarian cancer cell migration by activating epithelial-to-mesenchymal transition.

Authors:  L Teng; S Peng; H Guo; H Liang; Z Xu; Y Su; L Gao
Journal:  Cancer Gene Ther       Date:  2015-10-23       Impact factor: 5.987

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Authors:  Hidenori Kusumoto; Yasushi Shintani; Ryu Kanzaki; Tomohiro Kawamura; Soichiro Funaki; Masato Minami; Izumi Nagatomo; Eiichi Morii; Meinoshin Okumura
Journal:  Cancer Sci       Date:  2017-03       Impact factor: 6.716

4.  Marked epithelial to mesenchymal transition in surgical margins of oral cancer-an in vitro study.

Authors:  Milos Lazarevic; Maja Milosevic; Drago Jelovac; Sanja Milenkovic; Zvezdana Tepavcevic; Federica Baldan; Tijana Suboticki; Bosko Toljic; Dijana Trisic; Miroslav Dragovic; Giuseppe Damante; Jelena Milasin
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5.  Expression ratio of the TGFβ-inducible gene MYO10 is prognostic for overall survival of squamous cell lung cancer patients and predicts chemotherapy response.

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Journal:  Sci Rep       Date:  2018-06-22       Impact factor: 4.379

  5 in total

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