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Molecularly-targeted therapy for the oral cancer stem cells
Human cancer tissues are heterogeneous in nature and become differentiated during expansion of cancer stem cells (CSCs). CSCs initiate tumorigenesis, and are involved in tumor recurrence and metastasis. Furthermore, data show that CSCs are highly resistant to anticancer drugs. Cetuximab, a specific...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944082/ https://www.ncbi.nlm.nih.gov/pubmed/29755619 http://dx.doi.org/10.1016/j.jdsr.2017.11.001 |
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author | Ohnishi, Yuichi Yasui, Hiroki Nozaki, Masami Nakajima, Masahiro |
author_facet | Ohnishi, Yuichi Yasui, Hiroki Nozaki, Masami Nakajima, Masahiro |
author_sort | Ohnishi, Yuichi |
collection | PubMed |
description | Human cancer tissues are heterogeneous in nature and become differentiated during expansion of cancer stem cells (CSCs). CSCs initiate tumorigenesis, and are involved in tumor recurrence and metastasis. Furthermore, data show that CSCs are highly resistant to anticancer drugs. Cetuximab, a specific anti-epidermal growth factor receptor (EGFR) monoclonal antibody, is used in cancer treatment. Although development of resistance to cetuximab is well recognized, the underlying mechanisms remain unclear. Lapatinib, a dual inhibitor of epidermal growth factor receptor (EGFR)/ErbB2, has antiproliferative effects and is used to treat patients with ErbB2-positive metastatic breast cancer. In this review, cetuximab and lapatinib-resistant oral squamous cell carcinoma (OSCC) cells proliferation and migration signal transduction passway is discussed by introducing our research. |
format | Online Article Text |
id | pubmed-5944082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-59440822018-05-11 Molecularly-targeted therapy for the oral cancer stem cells Ohnishi, Yuichi Yasui, Hiroki Nozaki, Masami Nakajima, Masahiro Jpn Dent Sci Rev Review Article Human cancer tissues are heterogeneous in nature and become differentiated during expansion of cancer stem cells (CSCs). CSCs initiate tumorigenesis, and are involved in tumor recurrence and metastasis. Furthermore, data show that CSCs are highly resistant to anticancer drugs. Cetuximab, a specific anti-epidermal growth factor receptor (EGFR) monoclonal antibody, is used in cancer treatment. Although development of resistance to cetuximab is well recognized, the underlying mechanisms remain unclear. Lapatinib, a dual inhibitor of epidermal growth factor receptor (EGFR)/ErbB2, has antiproliferative effects and is used to treat patients with ErbB2-positive metastatic breast cancer. In this review, cetuximab and lapatinib-resistant oral squamous cell carcinoma (OSCC) cells proliferation and migration signal transduction passway is discussed by introducing our research. Elsevier 2018-05 2017-12-16 /pmc/articles/PMC5944082/ /pubmed/29755619 http://dx.doi.org/10.1016/j.jdsr.2017.11.001 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Article Ohnishi, Yuichi Yasui, Hiroki Nozaki, Masami Nakajima, Masahiro Molecularly-targeted therapy for the oral cancer stem cells |
title | Molecularly-targeted therapy for the oral cancer stem cells |
title_full | Molecularly-targeted therapy for the oral cancer stem cells |
title_fullStr | Molecularly-targeted therapy for the oral cancer stem cells |
title_full_unstemmed | Molecularly-targeted therapy for the oral cancer stem cells |
title_short | Molecularly-targeted therapy for the oral cancer stem cells |
title_sort | molecularly-targeted therapy for the oral cancer stem cells |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944082/ https://www.ncbi.nlm.nih.gov/pubmed/29755619 http://dx.doi.org/10.1016/j.jdsr.2017.11.001 |
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