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CD44v8-10 as a potential theranostic biomarker for targeting disseminated cancer cells in advanced gastric cancer
Gastric cancer is the third most common cause of cancer mortality, and the survival rate of stage IV advanced gastric cancer (AGC) patients with distant metastasis is very low. Thus, the detection and eradication of disseminated cancer cells by targeting cell surface molecules in AGC would improve p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503939/ https://www.ncbi.nlm.nih.gov/pubmed/28694503 http://dx.doi.org/10.1038/s41598-017-05247-7 |
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author | Choi, Eun-Seok Kim, Hyunjin Kim, Hyung-Pyo Choi, Yongdoo Goh, Sung-Ho |
author_facet | Choi, Eun-Seok Kim, Hyunjin Kim, Hyung-Pyo Choi, Yongdoo Goh, Sung-Ho |
author_sort | Choi, Eun-Seok |
collection | PubMed |
description | Gastric cancer is the third most common cause of cancer mortality, and the survival rate of stage IV advanced gastric cancer (AGC) patients with distant metastasis is very low. Thus, the detection and eradication of disseminated cancer cells by targeting cell surface molecules in AGC would improve patient survival. The hyaluronic acid receptor, CD44, has various isoforms generated by alternative splicing, and some isoforms are known to be correlated to gastric cancer. In this study, to find out the most appropriate CD44v for targeting AGC, we analysed the expression differences of CD44 isoforms at the mRNA level in stomach cancer cell lines as well as in 74 patients with AGC by using exon-specific qRT-PCR. Among the CD44v isoforms, CD44v8-10 was determined as the most promising biomarker for the development of theranostic agents of gastric cancer. Next, we synthesised the conjugate of anti-CD44v9 antibody with near-infrared fluorophore or photosensitiser, and then demonstrated its feasibility for target cell-specific imaging and photoimmunotherapy in gastric cancer. As a result, these conjugates have clearly demarcated the surface of CD44v8-10 expressing cancer cells and showed efficient phototoxic effects. Therefore, this study revealed that CD44v8-10 is the efficient theranostic biomarker to target disseminated cancer cells in AGC. |
format | Online Article Text |
id | pubmed-5503939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55039392017-07-12 CD44v8-10 as a potential theranostic biomarker for targeting disseminated cancer cells in advanced gastric cancer Choi, Eun-Seok Kim, Hyunjin Kim, Hyung-Pyo Choi, Yongdoo Goh, Sung-Ho Sci Rep Article Gastric cancer is the third most common cause of cancer mortality, and the survival rate of stage IV advanced gastric cancer (AGC) patients with distant metastasis is very low. Thus, the detection and eradication of disseminated cancer cells by targeting cell surface molecules in AGC would improve patient survival. The hyaluronic acid receptor, CD44, has various isoforms generated by alternative splicing, and some isoforms are known to be correlated to gastric cancer. In this study, to find out the most appropriate CD44v for targeting AGC, we analysed the expression differences of CD44 isoforms at the mRNA level in stomach cancer cell lines as well as in 74 patients with AGC by using exon-specific qRT-PCR. Among the CD44v isoforms, CD44v8-10 was determined as the most promising biomarker for the development of theranostic agents of gastric cancer. Next, we synthesised the conjugate of anti-CD44v9 antibody with near-infrared fluorophore or photosensitiser, and then demonstrated its feasibility for target cell-specific imaging and photoimmunotherapy in gastric cancer. As a result, these conjugates have clearly demarcated the surface of CD44v8-10 expressing cancer cells and showed efficient phototoxic effects. Therefore, this study revealed that CD44v8-10 is the efficient theranostic biomarker to target disseminated cancer cells in AGC. Nature Publishing Group UK 2017-07-10 /pmc/articles/PMC5503939/ /pubmed/28694503 http://dx.doi.org/10.1038/s41598-017-05247-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Choi, Eun-Seok Kim, Hyunjin Kim, Hyung-Pyo Choi, Yongdoo Goh, Sung-Ho CD44v8-10 as a potential theranostic biomarker for targeting disseminated cancer cells in advanced gastric cancer |
title | CD44v8-10 as a potential theranostic biomarker for targeting disseminated cancer cells in advanced gastric cancer |
title_full | CD44v8-10 as a potential theranostic biomarker for targeting disseminated cancer cells in advanced gastric cancer |
title_fullStr | CD44v8-10 as a potential theranostic biomarker for targeting disseminated cancer cells in advanced gastric cancer |
title_full_unstemmed | CD44v8-10 as a potential theranostic biomarker for targeting disseminated cancer cells in advanced gastric cancer |
title_short | CD44v8-10 as a potential theranostic biomarker for targeting disseminated cancer cells in advanced gastric cancer |
title_sort | cd44v8-10 as a potential theranostic biomarker for targeting disseminated cancer cells in advanced gastric cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503939/ https://www.ncbi.nlm.nih.gov/pubmed/28694503 http://dx.doi.org/10.1038/s41598-017-05247-7 |
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