Document Detail


Transforming potential and matrix stiffness co-regulate confinement sensitivity of tumor cell migration.
MedLine Citation:
PMID:  23832051     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
It is now well established that tumor cell invasion through tissue is strongly regulated by the microstructural and mechanical properties of the extracellular matrix (ECM). However, it remains unclear how these physical microenvironmental inputs are jointly processed with oncogenic lesions to drive invasion. In this study, we address this open question by combining a microfabricated polyacrylamide channel (μPAC) platform that enables independent control of ECM stiffness and confinement with an isogenically-matched breast tumor progression series in which the oncogenes ErbB2 and 14-3-3ζ are overexpressed independently or in tandem. We find that increasing channel confinement and overexpressing ErbB2 both promote cell migration to a similar degree when other parameters are kept constant. In contrast, 14-3-3ζ overexpression slows migration speed, and does so in a fashion that dwarfs effects of ECM confinement and stiffness. We also find that ECM stiffness dramatically enhances cell motility when combined with ErbB2 overexpression, demonstrating that biophysical cues and cell-intrinsic parameters promote cell invasion in an integrative manner. Morphometric analysis of cells inside the μPAC platform reveals that the rapid cell migration induced by narrow channels and ErbB2 overexpression are both accompanied by increased cell polarization. Disruption of this polarization occurs by pharmacological inhibition of Rac GTPase phenocopies 14-3-3ζ overexpression by reducing cell polarization and slowing migration. By systematically measuring migration speed as a function of matrix stiffness and confinement, we also quantify for the first time the sensitivity of migration speed to microchannel properties and transforming potential. These results demonstrate that oncogenic lesions and ECM biophysical properties can synergistically interact to drive invasive migration, and that both inputs may act through common molecular mechanisms to enhance migration speed.
Authors:
Amit Pathak; Sanjay Kumar
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  Integrative biology : quantitative biosciences from nano to macro     Volume:  5     ISSN:  1757-9708     ISO Abbreviation:  Integr Biol (Camb)     Publication Date:  2013 Aug 
Date Detail:
Created Date:  2013-07-23     Completed Date:  2014-02-10     Revised Date:  2014-08-25    
Medline Journal Info:
Nlm Unique ID:  101478378     Medline TA:  Integr Biol (Camb)     Country:  England    
Other Details:
Languages:  eng     Pagination:  1067-75     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
14-3-3 Proteins / metabolism
Acrylic Resins / chemistry
Cell Culture Techniques
Cell Line, Tumor
Cell Movement / physiology*
Cell Transformation, Neoplastic / pathology
Extracellular Matrix / physiology*
Humans
Hydrogel / chemistry
Microscopy, Confocal
Microscopy, Phase-Contrast
Neoplasm Invasiveness
Neoplasm Metastasis
Neoplasms / pathology*
Receptor, erbB-2 / metabolism
Silicon / chemistry
rac GTP-Binding Proteins / metabolism
Grant Support
ID/Acronym/Agency:
1DP2OD004213/OD/NIH HHS; 1U54CA143836/CA/NCI NIH HHS; DP2 OD004213/OD/NIH HHS
Chemical
Reg. No./Substance:
0/14-3-3 Proteins; 0/Acrylic Resins; 25852-47-5/Hydrogel; 9003-05-8/polyacrylamide; EC 2.7.10.1/Receptor, erbB-2; EC 3.6.5.2/rac GTP-Binding Proteins; Z4152N8IUI/Silicon
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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