Molecular pathways and therapeutic targets in lung cancer
Lung cancer is still the leading cause of cancer death worldwide. Both histologically and molecularly lung cancer is heterogeneous. This review summarizes the current knowledge of the pathways involved in the various types of lung cancer with an emphasis on the clinical implications of the increasin...
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Published in | Oncotarget Vol. 5; no. 6; pp. 1392 - 1433 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Impact Journals LLC
30.03.2014
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Subjects | |
Online Access | Get full text |
ISSN | 1949-2553 1949-2553 |
DOI | 10.18632/oncotarget.1891 |
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Abstract | Lung cancer is still the leading cause of cancer death worldwide. Both histologically and molecularly lung cancer is heterogeneous. This review summarizes the current knowledge of the pathways involved in the various types of lung cancer with an emphasis on the clinical implications of the increasing number of actionable molecular targets. It describes the major pathways and molecular alterations implicated in the development and progression of non-small cell lung cancer (adenocarcinoma and squamous cancer), and of small cell carcinoma, emphasizing the molecular alterations comprising the specific blueprints in each group. The approved and investigational targeted therapies as well as the immune therapies, and clinical trials exploring the variety of targeted approaches to treatment of lung cancer are the main focus of this review. |
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AbstractList | Lung cancer is still the leading cause of cancer death worldwide. Both histologically and molecularly lung cancer is heterogeneous. This review summarizes the current knowledge of the pathways involved in the various types of lung cancer with an emphasis on the clinical implications of the increasing number of actionable molecular targets. It describes the major pathways and molecular alterations implicated in the development and progression of non-small cell lung cancer (adenocarcinoma and squamous cancer), and of small cell carcinoma, emphasizing the molecular alterations comprising the specific blueprints in each group. The approved and investigational targeted therapies as well as the immune therapies, and clinical trials exploring the variety of targeted approaches to treatment of lung cancer are the main focus of this review. Lung cancer is still the leading cause of cancer death worldwide. Both histologically and molecularly lung cancer is heterogeneous. This review summarizes the current knowledge of the pathways involved in the various types of lung cancer with an emphasis on the clinical implications of the increasing number of actionable molecular targets. It describes the major pathways and molecular alterations implicated in the development and progression of non-small cell lung cancer (adenocarcinoma and squamous cancer), and of small cell carcinoma, emphasizing the molecular alterations comprising the specific blueprints in each group. The approved and investigational targeted therapies as well as the immune therapies, and clinical trials exploring the variety of targeted approaches to treatment of lung cancer are the main focus of this review.Lung cancer is still the leading cause of cancer death worldwide. Both histologically and molecularly lung cancer is heterogeneous. This review summarizes the current knowledge of the pathways involved in the various types of lung cancer with an emphasis on the clinical implications of the increasing number of actionable molecular targets. It describes the major pathways and molecular alterations implicated in the development and progression of non-small cell lung cancer (adenocarcinoma and squamous cancer), and of small cell carcinoma, emphasizing the molecular alterations comprising the specific blueprints in each group. The approved and investigational targeted therapies as well as the immune therapies, and clinical trials exploring the variety of targeted approaches to treatment of lung cancer are the main focus of this review. |
Author | Bueno, Raphael Simon, George R. Otterson, Gregory A. Shtivelman, Emma Dennis, Phillip A. Hensing, Thomas Salgia, Ravi |
AuthorAffiliation | 1 Cancer Commons, Palo Alto, CA, United States of America 7 Department of Medicine, Section of Hematology/Oncology, University of Chicago, United States of America 2 Northshore University Health System and University of Chicago, United States of America 4 Johns Hopkins University School of Medicine, United States of America 3 MD Anderson Cancer Center, United States of America 5 Ohio State University Comprehensive Cancer Center, United States of America 6 Brigham & Women's Hospital, Harvard Medical School, United States of America |
AuthorAffiliation_xml | – name: 1 Cancer Commons, Palo Alto, CA, United States of America – name: 4 Johns Hopkins University School of Medicine, United States of America – name: 3 MD Anderson Cancer Center, United States of America – name: 5 Ohio State University Comprehensive Cancer Center, United States of America – name: 2 Northshore University Health System and University of Chicago, United States of America – name: 7 Department of Medicine, Section of Hematology/Oncology, University of Chicago, United States of America – name: 6 Brigham & Women's Hospital, Harvard Medical School, United States of America |
Author_xml | – sequence: 1 givenname: Emma surname: Shtivelman fullname: Shtivelman, Emma organization: Cancer Commons, Palo Alto, CA, United States of America – sequence: 2 givenname: Thomas surname: Hensing fullname: Hensing, Thomas organization: Northshore University Health System and University of Chicago, United States of America – sequence: 3 givenname: George R. surname: Simon fullname: Simon, George R. organization: MD Anderson Cancer Center, United States of America – sequence: 4 givenname: Phillip A. surname: Dennis fullname: Dennis, Phillip A. organization: Johns Hopkins University School of Medicine, United States of America – sequence: 5 givenname: Gregory A. surname: Otterson fullname: Otterson, Gregory A. organization: Ohio State University Comprehensive Cancer Center, United States of America – sequence: 6 givenname: Raphael surname: Bueno fullname: Bueno, Raphael organization: Brigham & Women's Hospital, Harvard Medical School, United States of America – sequence: 7 givenname: Ravi surname: Salgia fullname: Salgia, Ravi organization: Department of Medicine, Section of Hematology/Oncology, University of Chicago, United States of America |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24722523$$D View this record in MEDLINE/PubMed |
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Snippet | Lung cancer is still the leading cause of cancer death worldwide. Both histologically and molecularly lung cancer is heterogeneous. This review summarizes the... |
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SubjectTerms | Animals Antineoplastic Agents - therapeutic use Humans Molecular Targeted Therapy Neoplasm Proteins - antagonists & inhibitors Neoplasm Proteins - metabolism Neoplasms - drug therapy Neoplasms - metabolism Neoplasms - pathology Review Signal Transduction - drug effects |
Title | Molecular pathways and therapeutic targets in lung cancer |
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