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The Study of a Novel Sorafenib Derivative HLC-080 as an Antitumor Agent
In this study, our objective is to evaluate the potential of a novel Sorafenib derivative, named HLC-080, as a new anticancer agent for colon cancer. We firstly carried out MTT assay, colony formation assay, flow cytometry analysis and transwell invasion assay to determine effect of our compound HLC...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086976/ https://www.ncbi.nlm.nih.gov/pubmed/25004130 http://dx.doi.org/10.1371/journal.pone.0101889 |
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author | Tang, Ke Luo, Can Li, Yan Lu, Chenshu Zhou, Wanqi Huang, Haihong Chen, Xiaoguang |
author_facet | Tang, Ke Luo, Can Li, Yan Lu, Chenshu Zhou, Wanqi Huang, Haihong Chen, Xiaoguang |
author_sort | Tang, Ke |
collection | PubMed |
description | In this study, our objective is to evaluate the potential of a novel Sorafenib derivative, named HLC-080, as a new anticancer agent for colon cancer. We firstly carried out MTT assay, colony formation assay, flow cytometry analysis and transwell invasion assay to determine effect of our compound HLC-080 on cell viability, anti-proliferation activity, cell cycle arrest and the intervention on cell invasion, respectively. On the other hand, in vivo antitumor activity of HLC-080 was also tested using H22 xenograft model and the angiogenesis effect of HLC-080 was measured by EA.hy926 tube formation assay. The expression levels of various proteins in HLC-080 treated with HT-29 cell lines were examined using Western blot and ELISA experiments. The results showed that HLC-080 could dramatically inhibit the growth and colony formation of various tumor cells, therefore exhibited remarkable antitumor activity. HLC-080 can induce cell cycle arrest at G1 phase in HT-29 cells and subsequently inhibit the invasive potential of colon cancer cells. HLC-080 also exhibits anti-angiogenesis effect in EA.hy926 model. Additionally, the in vivo study showed that HLC-080 was able to reduced the tumor weight with the rate of 35.81%. And at the concentration of 0.352±0.034 µM, HLC-080 is able to reduce half of the regular protein level of p-c-Raf (Ser259), consequently block Raf/MEK/ERK signaling in HT-29 cell lines. In conclusion, our study suggests that Sorafenib derivative HLC-080 has the potential to inhibit cell proliferation and angiogenesis, Since, HLC-080 is particularly active against human colon cancer cells, our study highlights that HLC-080 and its related analogues may serve as a new anti-cancer drug, particularly against colon cancer. |
format | Online Article Text |
id | pubmed-4086976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40869762014-07-14 The Study of a Novel Sorafenib Derivative HLC-080 as an Antitumor Agent Tang, Ke Luo, Can Li, Yan Lu, Chenshu Zhou, Wanqi Huang, Haihong Chen, Xiaoguang PLoS One Research Article In this study, our objective is to evaluate the potential of a novel Sorafenib derivative, named HLC-080, as a new anticancer agent for colon cancer. We firstly carried out MTT assay, colony formation assay, flow cytometry analysis and transwell invasion assay to determine effect of our compound HLC-080 on cell viability, anti-proliferation activity, cell cycle arrest and the intervention on cell invasion, respectively. On the other hand, in vivo antitumor activity of HLC-080 was also tested using H22 xenograft model and the angiogenesis effect of HLC-080 was measured by EA.hy926 tube formation assay. The expression levels of various proteins in HLC-080 treated with HT-29 cell lines were examined using Western blot and ELISA experiments. The results showed that HLC-080 could dramatically inhibit the growth and colony formation of various tumor cells, therefore exhibited remarkable antitumor activity. HLC-080 can induce cell cycle arrest at G1 phase in HT-29 cells and subsequently inhibit the invasive potential of colon cancer cells. HLC-080 also exhibits anti-angiogenesis effect in EA.hy926 model. Additionally, the in vivo study showed that HLC-080 was able to reduced the tumor weight with the rate of 35.81%. And at the concentration of 0.352±0.034 µM, HLC-080 is able to reduce half of the regular protein level of p-c-Raf (Ser259), consequently block Raf/MEK/ERK signaling in HT-29 cell lines. In conclusion, our study suggests that Sorafenib derivative HLC-080 has the potential to inhibit cell proliferation and angiogenesis, Since, HLC-080 is particularly active against human colon cancer cells, our study highlights that HLC-080 and its related analogues may serve as a new anti-cancer drug, particularly against colon cancer. Public Library of Science 2014-07-08 /pmc/articles/PMC4086976/ /pubmed/25004130 http://dx.doi.org/10.1371/journal.pone.0101889 Text en © 2014 Tang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tang, Ke Luo, Can Li, Yan Lu, Chenshu Zhou, Wanqi Huang, Haihong Chen, Xiaoguang The Study of a Novel Sorafenib Derivative HLC-080 as an Antitumor Agent |
title | The Study of a Novel Sorafenib Derivative HLC-080 as an Antitumor Agent |
title_full | The Study of a Novel Sorafenib Derivative HLC-080 as an Antitumor Agent |
title_fullStr | The Study of a Novel Sorafenib Derivative HLC-080 as an Antitumor Agent |
title_full_unstemmed | The Study of a Novel Sorafenib Derivative HLC-080 as an Antitumor Agent |
title_short | The Study of a Novel Sorafenib Derivative HLC-080 as an Antitumor Agent |
title_sort | study of a novel sorafenib derivative hlc-080 as an antitumor agent |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086976/ https://www.ncbi.nlm.nih.gov/pubmed/25004130 http://dx.doi.org/10.1371/journal.pone.0101889 |
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