Cargando…
PAI-1-Dependent Inactivation of SMAD4-Modulated Junction and Adhesion Complex in Obese Endometrial Cancer
While plasminogen activator inhibitor-1 (PAI-1) is known to potentiate cellular migration via proteolytic regulation, this adipokine is implicated as an oncogenic ligand in the tumor microenvironment. To understand the underlying paracrine mechanism, here, we conduct transcriptomic analysis of 1,898...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641039/ https://www.ncbi.nlm.nih.gov/pubmed/33053339 http://dx.doi.org/10.1016/j.celrep.2020.108253 |
_version_ | 1783605855774572544 |
---|---|
author | Lin, Li-Ling Kost, Edward R. Lin, Chun-Lin Valente, Philip Wang, Chiou-Miin Kolonin, Mikhail G. Daquinag, Alexes C. Tan, Xi Lucio, Nicholas Hung, Chia-Nung Wang, Chen-Pin Kirma, Nameer B. Huang, Tim H.-M. |
author_facet | Lin, Li-Ling Kost, Edward R. Lin, Chun-Lin Valente, Philip Wang, Chiou-Miin Kolonin, Mikhail G. Daquinag, Alexes C. Tan, Xi Lucio, Nicholas Hung, Chia-Nung Wang, Chen-Pin Kirma, Nameer B. Huang, Tim H.-M. |
author_sort | Lin, Li-Ling |
collection | PubMed |
description | While plasminogen activator inhibitor-1 (PAI-1) is known to potentiate cellular migration via proteolytic regulation, this adipokine is implicated as an oncogenic ligand in the tumor microenvironment. To understand the underlying paracrine mechanism, here, we conduct transcriptomic analysis of 1,898 endometrial epithelial cells (EECs) exposed and unexposed to PAI-1-secreting adipose stromal cells. The PAI-1-dependent action deregulates crosstalk among tumor-promoting and tumor-repressing pathways, including transforming growth factor β (TGF-β). When PAI-1 is tethered to lipoprotein receptor-related protein 1 (LRP1), the internalized signaling causes downregulation of SMAD4 at the transcriptional and post-translational levels that attenuates TGF-β-related transcription programs. Repression of genes encoding the junction and adhesion complex preferentially occurs in SMAD4-underexpressed EECs of persons with obesity. The findings highlight a role of PAI-1 signaling that renders ineffective intercellular communication for the development of adiposity-associated endometrial cancer. |
format | Online Article Text |
id | pubmed-7641039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76410392020-11-04 PAI-1-Dependent Inactivation of SMAD4-Modulated Junction and Adhesion Complex in Obese Endometrial Cancer Lin, Li-Ling Kost, Edward R. Lin, Chun-Lin Valente, Philip Wang, Chiou-Miin Kolonin, Mikhail G. Daquinag, Alexes C. Tan, Xi Lucio, Nicholas Hung, Chia-Nung Wang, Chen-Pin Kirma, Nameer B. Huang, Tim H.-M. Cell Rep Article While plasminogen activator inhibitor-1 (PAI-1) is known to potentiate cellular migration via proteolytic regulation, this adipokine is implicated as an oncogenic ligand in the tumor microenvironment. To understand the underlying paracrine mechanism, here, we conduct transcriptomic analysis of 1,898 endometrial epithelial cells (EECs) exposed and unexposed to PAI-1-secreting adipose stromal cells. The PAI-1-dependent action deregulates crosstalk among tumor-promoting and tumor-repressing pathways, including transforming growth factor β (TGF-β). When PAI-1 is tethered to lipoprotein receptor-related protein 1 (LRP1), the internalized signaling causes downregulation of SMAD4 at the transcriptional and post-translational levels that attenuates TGF-β-related transcription programs. Repression of genes encoding the junction and adhesion complex preferentially occurs in SMAD4-underexpressed EECs of persons with obesity. The findings highlight a role of PAI-1 signaling that renders ineffective intercellular communication for the development of adiposity-associated endometrial cancer. 2020-10-13 /pmc/articles/PMC7641039/ /pubmed/33053339 http://dx.doi.org/10.1016/j.celrep.2020.108253 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Lin, Li-Ling Kost, Edward R. Lin, Chun-Lin Valente, Philip Wang, Chiou-Miin Kolonin, Mikhail G. Daquinag, Alexes C. Tan, Xi Lucio, Nicholas Hung, Chia-Nung Wang, Chen-Pin Kirma, Nameer B. Huang, Tim H.-M. PAI-1-Dependent Inactivation of SMAD4-Modulated Junction and Adhesion Complex in Obese Endometrial Cancer |
title | PAI-1-Dependent Inactivation of SMAD4-Modulated Junction and Adhesion Complex in Obese Endometrial Cancer |
title_full | PAI-1-Dependent Inactivation of SMAD4-Modulated Junction and Adhesion Complex in Obese Endometrial Cancer |
title_fullStr | PAI-1-Dependent Inactivation of SMAD4-Modulated Junction and Adhesion Complex in Obese Endometrial Cancer |
title_full_unstemmed | PAI-1-Dependent Inactivation of SMAD4-Modulated Junction and Adhesion Complex in Obese Endometrial Cancer |
title_short | PAI-1-Dependent Inactivation of SMAD4-Modulated Junction and Adhesion Complex in Obese Endometrial Cancer |
title_sort | pai-1-dependent inactivation of smad4-modulated junction and adhesion complex in obese endometrial cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641039/ https://www.ncbi.nlm.nih.gov/pubmed/33053339 http://dx.doi.org/10.1016/j.celrep.2020.108253 |
work_keys_str_mv | AT linliling pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT kostedwardr pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT linchunlin pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT valentephilip pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT wangchioumiin pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT koloninmikhailg pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT daquinagalexesc pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT tanxi pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT lucionicholas pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT hungchianung pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT wangchenpin pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT kirmanameerb pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer AT huangtimhm pai1dependentinactivationofsmad4modulatedjunctionandadhesioncomplexinobeseendometrialcancer |