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In vivo antitumor and antimetastatic effects of flavokawain B in 4T1 breast cancer cell-challenged mice

Flavokawain B (FKB) is a naturally occurring chalcone that can be isolated through the root extracts of the kava-kava plant (Piper methysticum). It can also be synthesized chemically to increase the yield. This compound is a promising candidate as a biological agent, as it is reported to be involved...

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Autores principales: Abu, Nadiah, Mohamed, Nurul Elyani, Yeap, Swee Keong, Lim, Kian Lam, Akhtar, M Nadeem, Zulfadli, Aimi Jamil, Kee, Beh Boon, Abdullah, Mohd Puad, Omar, Abdul Rahman, Alitheen, Noorjahan Banu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358690/
https://www.ncbi.nlm.nih.gov/pubmed/25834398
http://dx.doi.org/10.2147/DDDT.S67976
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author Abu, Nadiah
Mohamed, Nurul Elyani
Yeap, Swee Keong
Lim, Kian Lam
Akhtar, M Nadeem
Zulfadli, Aimi Jamil
Kee, Beh Boon
Abdullah, Mohd Puad
Omar, Abdul Rahman
Alitheen, Noorjahan Banu
author_facet Abu, Nadiah
Mohamed, Nurul Elyani
Yeap, Swee Keong
Lim, Kian Lam
Akhtar, M Nadeem
Zulfadli, Aimi Jamil
Kee, Beh Boon
Abdullah, Mohd Puad
Omar, Abdul Rahman
Alitheen, Noorjahan Banu
author_sort Abu, Nadiah
collection PubMed
description Flavokawain B (FKB) is a naturally occurring chalcone that can be isolated through the root extracts of the kava-kava plant (Piper methysticum). It can also be synthesized chemically to increase the yield. This compound is a promising candidate as a biological agent, as it is reported to be involved in a wide range of biological activities. Furthermore, FKB was reported to have antitumorigenic effects in several cancer cell lines in vitro. However, the in vivo antitumor effects of FKB have not been reported on yet. Breast cancer is one of the major causes of cancer-related deaths in the world today. Any potential treatment should not only impede the growth of the tumor, but also modulate the immune system efficiently and inhibit the formation of secondary tumors. As presented in our study, FKB induced apoptosis in 4T1 tumors in vivo, as evidenced by the terminal deoxynucleotidyl transferase dUTP nick end labeling and hematoxylin and eosin staining of the tumor. FKB also regulated the immune system by increasing both helper and cytolytic T-cell and natural killer cell populations. In addition, FKB also enhanced the levels of interleukin 2 and interferon gamma but suppressed interleukin 1B. Apart from that, FKB was also found to inhibit metastasis, as evaluated by clonogenic assay, bone marrow smearing assay, real-time polymerase chain reaction, Western blot, and proteome profiler analysis. All in all, FKB may serve as a promising anticancer agent, especially in treating breast cancer.
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spelling pubmed-43586902015-04-01 In vivo antitumor and antimetastatic effects of flavokawain B in 4T1 breast cancer cell-challenged mice Abu, Nadiah Mohamed, Nurul Elyani Yeap, Swee Keong Lim, Kian Lam Akhtar, M Nadeem Zulfadli, Aimi Jamil Kee, Beh Boon Abdullah, Mohd Puad Omar, Abdul Rahman Alitheen, Noorjahan Banu Drug Des Devel Ther Original Research Flavokawain B (FKB) is a naturally occurring chalcone that can be isolated through the root extracts of the kava-kava plant (Piper methysticum). It can also be synthesized chemically to increase the yield. This compound is a promising candidate as a biological agent, as it is reported to be involved in a wide range of biological activities. Furthermore, FKB was reported to have antitumorigenic effects in several cancer cell lines in vitro. However, the in vivo antitumor effects of FKB have not been reported on yet. Breast cancer is one of the major causes of cancer-related deaths in the world today. Any potential treatment should not only impede the growth of the tumor, but also modulate the immune system efficiently and inhibit the formation of secondary tumors. As presented in our study, FKB induced apoptosis in 4T1 tumors in vivo, as evidenced by the terminal deoxynucleotidyl transferase dUTP nick end labeling and hematoxylin and eosin staining of the tumor. FKB also regulated the immune system by increasing both helper and cytolytic T-cell and natural killer cell populations. In addition, FKB also enhanced the levels of interleukin 2 and interferon gamma but suppressed interleukin 1B. Apart from that, FKB was also found to inhibit metastasis, as evaluated by clonogenic assay, bone marrow smearing assay, real-time polymerase chain reaction, Western blot, and proteome profiler analysis. All in all, FKB may serve as a promising anticancer agent, especially in treating breast cancer. Dove Medical Press 2015-03-06 /pmc/articles/PMC4358690/ /pubmed/25834398 http://dx.doi.org/10.2147/DDDT.S67976 Text en © 2015 Abu et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Abu, Nadiah
Mohamed, Nurul Elyani
Yeap, Swee Keong
Lim, Kian Lam
Akhtar, M Nadeem
Zulfadli, Aimi Jamil
Kee, Beh Boon
Abdullah, Mohd Puad
Omar, Abdul Rahman
Alitheen, Noorjahan Banu
In vivo antitumor and antimetastatic effects of flavokawain B in 4T1 breast cancer cell-challenged mice
title In vivo antitumor and antimetastatic effects of flavokawain B in 4T1 breast cancer cell-challenged mice
title_full In vivo antitumor and antimetastatic effects of flavokawain B in 4T1 breast cancer cell-challenged mice
title_fullStr In vivo antitumor and antimetastatic effects of flavokawain B in 4T1 breast cancer cell-challenged mice
title_full_unstemmed In vivo antitumor and antimetastatic effects of flavokawain B in 4T1 breast cancer cell-challenged mice
title_short In vivo antitumor and antimetastatic effects of flavokawain B in 4T1 breast cancer cell-challenged mice
title_sort in vivo antitumor and antimetastatic effects of flavokawain b in 4t1 breast cancer cell-challenged mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358690/
https://www.ncbi.nlm.nih.gov/pubmed/25834398
http://dx.doi.org/10.2147/DDDT.S67976
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