The Inflammatory Tumor Microenvironment, Epithelial Mesenchymal Transition and Lung Carcinogenesis
The inflammatory tumor microenvironment (TME) has many roles in tumor progression and metastasis, including creation of a hypoxic environment, increased angiogenesis and invasion, changes in expression of microRNAs (miRNAs) and an increase in a stem cell phenotype. Each of these has an impact on epi...
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Published in | Cancer microenvironment Vol. 5; no. 1; pp. 5 - 18 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
Springer Netherlands
01.04.2012
Springer Nature B.V |
Subjects | |
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Abstract | The inflammatory tumor microenvironment (TME) has many roles in tumor progression and metastasis, including creation of a hypoxic environment, increased angiogenesis and invasion, changes in expression of microRNAs (miRNAs) and an increase in a stem cell phenotype. Each of these has an impact on epithelial mesenchymal transition (EMT), particularly through the downregulation of E-cadherin. Here we review seminal work and recent findings linking the role of inflammation in the TME, EMT and lung cancer initiation, progression and metastasis. Finally, we discuss the potential of targeting aspects of inflammation and EMT in cancer prevention and treatment. |
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AbstractList | The inflammatory tumor microenvironment (TME) has many roles in tumor progression and metastasis, including creation of a hypoxic environment, increased angiogenesis and invasion, changes in expression of microRNAs (miRNAs) and an increase in a stem cell phenotype. Each of these has an impact on epithelial mesenchymal transition (EMT), particularly through the downregulation of E-cadherin. Here we review seminal work and recent findings linking the role of inflammation in the TME, EMT and lung cancer initiation, progression and metastasis. Finally, we discuss the potential of targeting aspects of inflammation and EMT in cancer prevention and treatment. The inflammatory tumor microenvironment (TME) has many roles in tumor progression and metastasis, including creation of a hypoxic environment, increased angiogenesis and invasion, changes in expression of microRNAs (miRNAs) and an increase in a stem cell phenotype. Each of these has an impact on epithelial mesenchymal transition (EMT), particularly through the downregulation of E-cadherin. Here we review seminal work and recent findings linking the role of inflammation in the TME, EMT and lung cancer initiation, progression and metastasis. Finally, we discuss the potential of targeting aspects of inflammation and EMT in cancer prevention and treatment.[PUBLICATION ABSTRACT] |
Author | Krysan, Kostyantyn Dubinett, Steven M. Heinrich, Eileen L. Grant, Jeanette L. Liclican, Elvira L. Walser, Tonya C. Rodriguez, Nicole L. |
Author_xml | – sequence: 1 givenname: Eileen L. surname: Heinrich fullname: Heinrich, Eileen L. organization: Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA – sequence: 2 givenname: Tonya C. surname: Walser fullname: Walser, Tonya C. organization: Division of Pulmonary and Critical Care Medicine, David Geffen School of Medicine at UCLA, Department of Medicine, David Geffen School of Medicine at UCLA, The Lung Cancer Research Program of the Jonsson Comprehensive Cancer Center – sequence: 3 givenname: Kostyantyn surname: Krysan fullname: Krysan, Kostyantyn organization: Division of Pulmonary and Critical Care Medicine, David Geffen School of Medicine at UCLA, Department of Medicine, David Geffen School of Medicine at UCLA, The Lung Cancer Research Program of the Jonsson Comprehensive Cancer Center – sequence: 4 givenname: Elvira L. surname: Liclican fullname: Liclican, Elvira L. organization: Division of Pulmonary and Critical Care Medicine, David Geffen School of Medicine at UCLA, Department of Medicine, David Geffen School of Medicine at UCLA, The Lung Cancer Research Program of the Jonsson Comprehensive Cancer Center – sequence: 5 givenname: Jeanette L. surname: Grant fullname: Grant, Jeanette L. organization: Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA – sequence: 6 givenname: Nicole L. surname: Rodriguez fullname: Rodriguez, Nicole L. organization: Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA – sequence: 7 givenname: Steven M. surname: Dubinett fullname: Dubinett, Steven M. email: SDubinett@mednet.ucla.edu organization: Division of Pulmonary and Critical Care Medicine, David Geffen School of Medicine at UCLA, Department of Medicine, David Geffen School of Medicine at UCLA, Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at UCLA, The Lung Cancer Research Program of the Jonsson Comprehensive Cancer Center |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21922183$$D View this record in MEDLINE/PubMed |
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Title | The Inflammatory Tumor Microenvironment, Epithelial Mesenchymal Transition and Lung Carcinogenesis |
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