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Contextual extracellular cues promote tumor cell EMT and metastasis by regulating miR-200 family expression

Contextual extracellular cues promote tumor cell EMT and metastasis by regulating miR-200 family... Downloaded from genesdev.cshlp.org on November 30, 2021 - Published by Cold Spring Harbor Laboratory Press Contextual extracellular cues promote tumor cell EMT and metastasis by regulating miR-200 family expression 1 1,6 2,6 1 3,4 Don L. Gibbons, Wei Lin, Chad J. Creighton, Zain H. Rizvi, Philip A. Gregory, 3,4 1 5 2 Gregory J. Goodall, Nishan Thilaganathan, Liqin Du, Yiqun Zhang, 5 1,7 Alexander Pertsemlidis, and Jonathan M. Kurie Department of Thoracic/Head and Neck Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, 2 3 Texas 77030, USA; Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA; Division of Human Immunology, Centre for Cancer Biology, Hanson Institute, Adelaide, SA 5000 Australia; Discipline of Medicine, The University of Adelaide, Adelaide, SA 5005 Australia; Eugene McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA Metastatic disease is a primary cause of cancer-related death, and factors governing tumor cell metastasis have not been fully elucidated. Here, we address this question by using tumor cell lines derived from mice that develop metastatic lung adenocarcinoma owing to expression of mutant K-ras and p53. Despite having widespread somatic genetic alterations, http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Genes & Development Unpaywall

Contextual extracellular cues promote tumor cell EMT and metastasis by regulating miR-200 family expression

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Publisher
Unpaywall
ISSN
0890-9369
DOI
10.1101/gad.1820209
Publisher site
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Abstract

Downloaded from genesdev.cshlp.org on November 30, 2021 - Published by Cold Spring Harbor Laboratory Press Contextual extracellular cues promote tumor cell EMT and metastasis by regulating miR-200 family expression 1 1,6 2,6 1 3,4 Don L. Gibbons, Wei Lin, Chad J. Creighton, Zain H. Rizvi, Philip A. Gregory, 3,4 1 5 2 Gregory J. Goodall, Nishan Thilaganathan, Liqin Du, Yiqun Zhang, 5 1,7 Alexander Pertsemlidis, and Jonathan M. Kurie Department of Thoracic/Head and Neck Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, 2 3 Texas 77030, USA; Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA; Division of Human Immunology, Centre for Cancer Biology, Hanson Institute, Adelaide, SA 5000 Australia; Discipline of Medicine, The University of Adelaide, Adelaide, SA 5005 Australia; Eugene McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA Metastatic disease is a primary cause of cancer-related death, and factors governing tumor cell metastasis have not been fully elucidated. Here, we address this question by using tumor cell lines derived from mice that develop metastatic lung adenocarcinoma owing to expression of mutant K-ras and p53. Despite having widespread somatic genetic alterations,

Journal

Genes & DevelopmentUnpaywall

Published: Sep 15, 2009

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