Andrographolide as a template in the synthesis of new anticancer agents with potentially novel molecular targets

Using andrographolide (AGP) as a template, a series of semisynthetic analogues was synthesised for the discovery of new anticancer agent(s) with improved antitumour selectivity and potency. SRJ09, a lead compound displayed remarkable activity in the National Cancer Institute (NCI) of USA in vitro an...

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Main Authors: Stanslas, Johnson, Lim, Siang Hui, Wong, Charng Choon, Sagineedu, Sreenivasa Rao, Lajis, Nordin
Format: Article
Language:English
Published: Federation of American Societies for Experimental Biology 2010
Online Access:http://psasir.upm.edu.my/id/eprint/13108/1/Andrographolide%20as%20a%20template%20in%20the%20synthesis%20of%20new%20anticancer%20agents%20with%20potentially%20novel%20molecular%20targets.pdf
http://psasir.upm.edu.my/id/eprint/13108/
http://www.fasebj.org/cgi/content/meeting_abstract/24/1_MeetingAbstracts/773.2
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Institution: Universiti Putra Malaysia
Language: English
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spelling my.upm.eprints.131082015-11-26T00:20:37Z http://psasir.upm.edu.my/id/eprint/13108/ Andrographolide as a template in the synthesis of new anticancer agents with potentially novel molecular targets Stanslas, Johnson Lim, Siang Hui Wong, Charng Choon Sagineedu, Sreenivasa Rao Lajis, Nordin Using andrographolide (AGP) as a template, a series of semisynthetic analogues was synthesised for the discovery of new anticancer agent(s) with improved antitumour selectivity and potency. SRJ09, a lead compound displayed remarkable activity in the National Cancer Institute (NCI) of USA in vitro anticancer screen, particularly against breast and colon cancers. The treatment of MCF-7 breast and HCT-116 colon cancer cells with SRJ09 induced a G1 phase cell cycle arrest through the down-regulation of CDK-4 expression with concomitant up-regulation of p21 expression and without affecting the cyclin D1 expression. SRJ09 induced apoptotic cell death in both cells in a p53- and bcl-2-independent manner, implicating extrinsic apoptotic pathway. The compound showed impressive in vivo activity by delaying HCT-116 tumour xenograft growth in nude mice. Recently, a derivative of SRJ09, SRS07 showed vast improvement in the NCI anticancer activity screen compared with the parent compound. Additionally, NCI’s in silico COMPARE and SOM analyses revealed that the new AGP derivatives have potentially novel molecular target(s). These findings although preliminary they are highly suggestive SRS07 have a great potential to be developed into a clinical anticancer agent. This research is funded by the Ministry of Science, Technology and Innovation of Malaysia (MOSTI) under the IRPA and ScienceFund grant schemes. Federation of American Societies for Experimental Biology 2010 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/13108/1/Andrographolide%20as%20a%20template%20in%20the%20synthesis%20of%20new%20anticancer%20agents%20with%20potentially%20novel%20molecular%20targets.pdf Stanslas, Johnson and Lim, Siang Hui and Wong, Charng Choon and Sagineedu, Sreenivasa Rao and Lajis, Nordin (2010) Andrographolide as a template in the synthesis of new anticancer agents with potentially novel molecular targets. The FASEB Journal, 24. ISSN 0892-6638; ESSN: 1530-6860 http://www.fasebj.org/cgi/content/meeting_abstract/24/1_MeetingAbstracts/773.2
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description Using andrographolide (AGP) as a template, a series of semisynthetic analogues was synthesised for the discovery of new anticancer agent(s) with improved antitumour selectivity and potency. SRJ09, a lead compound displayed remarkable activity in the National Cancer Institute (NCI) of USA in vitro anticancer screen, particularly against breast and colon cancers. The treatment of MCF-7 breast and HCT-116 colon cancer cells with SRJ09 induced a G1 phase cell cycle arrest through the down-regulation of CDK-4 expression with concomitant up-regulation of p21 expression and without affecting the cyclin D1 expression. SRJ09 induced apoptotic cell death in both cells in a p53- and bcl-2-independent manner, implicating extrinsic apoptotic pathway. The compound showed impressive in vivo activity by delaying HCT-116 tumour xenograft growth in nude mice. Recently, a derivative of SRJ09, SRS07 showed vast improvement in the NCI anticancer activity screen compared with the parent compound. Additionally, NCI’s in silico COMPARE and SOM analyses revealed that the new AGP derivatives have potentially novel molecular target(s). These findings although preliminary they are highly suggestive SRS07 have a great potential to be developed into a clinical anticancer agent. This research is funded by the Ministry of Science, Technology and Innovation of Malaysia (MOSTI) under the IRPA and ScienceFund grant schemes.
format Article
author Stanslas, Johnson
Lim, Siang Hui
Wong, Charng Choon
Sagineedu, Sreenivasa Rao
Lajis, Nordin
spellingShingle Stanslas, Johnson
Lim, Siang Hui
Wong, Charng Choon
Sagineedu, Sreenivasa Rao
Lajis, Nordin
Andrographolide as a template in the synthesis of new anticancer agents with potentially novel molecular targets
author_facet Stanslas, Johnson
Lim, Siang Hui
Wong, Charng Choon
Sagineedu, Sreenivasa Rao
Lajis, Nordin
author_sort Stanslas, Johnson
title Andrographolide as a template in the synthesis of new anticancer agents with potentially novel molecular targets
title_short Andrographolide as a template in the synthesis of new anticancer agents with potentially novel molecular targets
title_full Andrographolide as a template in the synthesis of new anticancer agents with potentially novel molecular targets
title_fullStr Andrographolide as a template in the synthesis of new anticancer agents with potentially novel molecular targets
title_full_unstemmed Andrographolide as a template in the synthesis of new anticancer agents with potentially novel molecular targets
title_sort andrographolide as a template in the synthesis of new anticancer agents with potentially novel molecular targets
publisher Federation of American Societies for Experimental Biology
publishDate 2010
url http://psasir.upm.edu.my/id/eprint/13108/1/Andrographolide%20as%20a%20template%20in%20the%20synthesis%20of%20new%20anticancer%20agents%20with%20potentially%20novel%20molecular%20targets.pdf
http://psasir.upm.edu.my/id/eprint/13108/
http://www.fasebj.org/cgi/content/meeting_abstract/24/1_MeetingAbstracts/773.2
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