Emerging Therapeutic Biomarkers in Endometrial Cancer

Although clinical trials of molecular therapies targeting critical biomarkers (mTOR, epidermal growth factor receptor/epidermal growth factor receptor 2, and vascular endothelial growth factor) in endometrial cancer show modest effects, there are still challenges that might remain regarding primary/...

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Main Authors: Peixin Dong, Masanori Kaneuchi, Yosuke Konno, Hidemichi Watari, Satoko Sudo, Noriaki Sakuragi
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2013/130362
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spelling doaj-234ec24a3e5b471091f83b9bf211cd9e2020-11-24T22:32:34ZengHindawi LimitedBioMed Research International2314-61332314-61412013-01-01201310.1155/2013/130362130362Emerging Therapeutic Biomarkers in Endometrial CancerPeixin Dong0Masanori Kaneuchi1Yosuke Konno2Hidemichi Watari3Satoko Sudo4Noriaki Sakuragi5Department of Women’s Health Educational System, Hokkaido University School of Medicine, Hokkaido University, N15, W7, Sapporo 060-8638, JapanDepartment of Women’s Health Educational System, Hokkaido University School of Medicine, Hokkaido University, N15, W7, Sapporo 060-8638, JapanDepartment of Gynecology, Hokkaido University School of Medicine, Hokkaido University, N15, W7, Sapporo 060-8638, JapanDepartment of Gynecology, Hokkaido University School of Medicine, Hokkaido University, N15, W7, Sapporo 060-8638, JapanDepartment of Gynecology, Hokkaido University School of Medicine, Hokkaido University, N15, W7, Sapporo 060-8638, JapanDepartment of Gynecology, Hokkaido University School of Medicine, Hokkaido University, N15, W7, Sapporo 060-8638, JapanAlthough clinical trials of molecular therapies targeting critical biomarkers (mTOR, epidermal growth factor receptor/epidermal growth factor receptor 2, and vascular endothelial growth factor) in endometrial cancer show modest effects, there are still challenges that might remain regarding primary/acquired drug resistance and unexpected side effects on normal tissues. New studies that aim to target both genetic and epigenetic alterations (noncoding microRNA) underlying malignant properties of tumor cells and to specifically attack tumor cells using cell surface markers overexpressed in tumor tissue are emerging. More importantly, strategies that disrupt the cancer stem cell/epithelial-mesenchymal transition-dependent signals and reactivate antitumor immune responses would bring new hope for complete elimination of all cell compartments in endometrial cancer. We briefly review the current status of molecular therapies tested in clinical trials and mainly discuss the potential therapeutic candidates that are possibly used to develop more effective and specific therapies against endometrial cancer progression and metastasis.http://dx.doi.org/10.1155/2013/130362
collection DOAJ
language English
format Article
sources DOAJ
author Peixin Dong
Masanori Kaneuchi
Yosuke Konno
Hidemichi Watari
Satoko Sudo
Noriaki Sakuragi
spellingShingle Peixin Dong
Masanori Kaneuchi
Yosuke Konno
Hidemichi Watari
Satoko Sudo
Noriaki Sakuragi
Emerging Therapeutic Biomarkers in Endometrial Cancer
BioMed Research International
author_facet Peixin Dong
Masanori Kaneuchi
Yosuke Konno
Hidemichi Watari
Satoko Sudo
Noriaki Sakuragi
author_sort Peixin Dong
title Emerging Therapeutic Biomarkers in Endometrial Cancer
title_short Emerging Therapeutic Biomarkers in Endometrial Cancer
title_full Emerging Therapeutic Biomarkers in Endometrial Cancer
title_fullStr Emerging Therapeutic Biomarkers in Endometrial Cancer
title_full_unstemmed Emerging Therapeutic Biomarkers in Endometrial Cancer
title_sort emerging therapeutic biomarkers in endometrial cancer
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2013-01-01
description Although clinical trials of molecular therapies targeting critical biomarkers (mTOR, epidermal growth factor receptor/epidermal growth factor receptor 2, and vascular endothelial growth factor) in endometrial cancer show modest effects, there are still challenges that might remain regarding primary/acquired drug resistance and unexpected side effects on normal tissues. New studies that aim to target both genetic and epigenetic alterations (noncoding microRNA) underlying malignant properties of tumor cells and to specifically attack tumor cells using cell surface markers overexpressed in tumor tissue are emerging. More importantly, strategies that disrupt the cancer stem cell/epithelial-mesenchymal transition-dependent signals and reactivate antitumor immune responses would bring new hope for complete elimination of all cell compartments in endometrial cancer. We briefly review the current status of molecular therapies tested in clinical trials and mainly discuss the potential therapeutic candidates that are possibly used to develop more effective and specific therapies against endometrial cancer progression and metastasis.
url http://dx.doi.org/10.1155/2013/130362
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