MET targeted therapy for lung cancer: clinical development and future directions
Yan Feng,1,2 Patrick C Ma1–31Translational Hematology and Oncology Research, 2Solid Tumor Oncology, 3Aerodigestive Oncology Translational Research, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH, USAAbstract: MET, the receptor for hepatocyte growth factor, has been identified...
Guardado en:
Autores principales: | , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Dove Medical Press
2012
|
Materias: | |
Acceso en línea: | https://doaj.org/article/1198cbd4fa954096b42e0400a73a3c59 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:1198cbd4fa954096b42e0400a73a3c59 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:1198cbd4fa954096b42e0400a73a3c592021-12-02T00:58:42ZMET targeted therapy for lung cancer: clinical development and future directions1179-2728https://doaj.org/article/1198cbd4fa954096b42e0400a73a3c592012-08-01T00:00:00Zhttp://www.dovepress.com/met-targeted-therapy-for-lung-cancer-clinical-development-and-future-d-a10669https://doaj.org/toc/1179-2728Yan Feng,1,2 Patrick C Ma1–31Translational Hematology and Oncology Research, 2Solid Tumor Oncology, 3Aerodigestive Oncology Translational Research, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH, USAAbstract: MET, the receptor for hepatocyte growth factor, has been identified as a novel promising target in various human malignancies, including lung cancer. Research studies have demonstrated that MET signaling plays important physiologic roles in embryogenesis and early development, whereas its deregulation from an otherwise quiescent signaling state in mature adult tissues can lead to upregulated cell proliferation, survival, scattering, motility and migration, angiogenesis, invasion, and metastasis in tumorigenesis and tumor progression. The MET pathway can be activated through ligand (hepatocyte growth factor, HGF) or MET receptor overexpression, genomic amplification, MET mutations, and alternative splicing. A number of novel therapeutic agents that target the MET/hepatocyte growth factor pathway have been tested in early-phase clinical studies with promising results. Phase III studies of MET targeting agents have recently been initiated. This paper will review the MET signaling pathway and biology in lung cancer, and the recent clinical development and advances of MET/hepatocyte growth factor targeting agents. Emphasis will be placed on discussing various unanswered issues and key strategies needed to optimize further clinical development of MET targeting personalized lung cancer therapy.Keywords: MET, HGF, lung cancer, targeted therapyFeng YMa PCDove Medical PressarticleNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENLung Cancer: Targets and Therapy, Vol 2012, Iss default, Pp 53-67 (2012) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
spellingShingle |
Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Feng Y Ma PC MET targeted therapy for lung cancer: clinical development and future directions |
description |
Yan Feng,1,2 Patrick C Ma1–31Translational Hematology and Oncology Research, 2Solid Tumor Oncology, 3Aerodigestive Oncology Translational Research, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH, USAAbstract: MET, the receptor for hepatocyte growth factor, has been identified as a novel promising target in various human malignancies, including lung cancer. Research studies have demonstrated that MET signaling plays important physiologic roles in embryogenesis and early development, whereas its deregulation from an otherwise quiescent signaling state in mature adult tissues can lead to upregulated cell proliferation, survival, scattering, motility and migration, angiogenesis, invasion, and metastasis in tumorigenesis and tumor progression. The MET pathway can be activated through ligand (hepatocyte growth factor, HGF) or MET receptor overexpression, genomic amplification, MET mutations, and alternative splicing. A number of novel therapeutic agents that target the MET/hepatocyte growth factor pathway have been tested in early-phase clinical studies with promising results. Phase III studies of MET targeting agents have recently been initiated. This paper will review the MET signaling pathway and biology in lung cancer, and the recent clinical development and advances of MET/hepatocyte growth factor targeting agents. Emphasis will be placed on discussing various unanswered issues and key strategies needed to optimize further clinical development of MET targeting personalized lung cancer therapy.Keywords: MET, HGF, lung cancer, targeted therapy |
format |
article |
author |
Feng Y Ma PC |
author_facet |
Feng Y Ma PC |
author_sort |
Feng Y |
title |
MET targeted therapy for lung cancer: clinical development and future directions |
title_short |
MET targeted therapy for lung cancer: clinical development and future directions |
title_full |
MET targeted therapy for lung cancer: clinical development and future directions |
title_fullStr |
MET targeted therapy for lung cancer: clinical development and future directions |
title_full_unstemmed |
MET targeted therapy for lung cancer: clinical development and future directions |
title_sort |
met targeted therapy for lung cancer: clinical development and future directions |
publisher |
Dove Medical Press |
publishDate |
2012 |
url |
https://doaj.org/article/1198cbd4fa954096b42e0400a73a3c59 |
work_keys_str_mv |
AT fengy mettargetedtherapyforlungcancerclinicaldevelopmentandfuturedirections AT mapc mettargetedtherapyforlungcancerclinicaldevelopmentandfuturedirections |
_version_ |
1718403361389150208 |