Anti breast cancer properties and toxicity of Dillenia suffruticosa root aqueous extract in BALB/c mice

Objective To determine the anti-breast cancer activities and the safety oral consumption of Dillenia suffruticosa root aqueous extract (DRAE) in BALB/c mice. Methods In the anti-breast cancer study, female BALB/c mice were divided into five groups (n = 12), which were (1) positive control (with...

Full description

Bibliographic Details
Main Authors: Saiful Yazan, Latifah, Yong, Sze Ong, Zaaba, Nur Elena, Mohd Ali, Razana, Jhi, Biau Foo, Yin, Sim Tor
Format: Article
Language:English
Published: Asian Pacific Journal of Tropical Biomedicine Editorial Office 2015
Online Access:http://psasir.upm.edu.my/id/eprint/43781/
http://psasir.upm.edu.my/id/eprint/43781/1/1-s2.0-S2221169115002208-main.pdf
_version_ 1848850321044930560
author Saiful Yazan, Latifah
Yong, Sze Ong
Zaaba, Nur Elena
Mohd Ali, Razana
Jhi, Biau Foo
Yin, Sim Tor
author_facet Saiful Yazan, Latifah
Yong, Sze Ong
Zaaba, Nur Elena
Mohd Ali, Razana
Jhi, Biau Foo
Yin, Sim Tor
author_sort Saiful Yazan, Latifah
building UPM Institutional Repository
collection Online Access
description Objective To determine the anti-breast cancer activities and the safety oral consumption of Dillenia suffruticosa root aqueous extract (DRAE) in BALB/c mice. Methods In the anti-breast cancer study, female BALB/c mice were divided into five groups (n = 12), which were (1) positive control (with breast cancer, untreated), (2) negative control (without breast cancer, untreated) and other three groups of mice with breast cancer treated with 1 000, 500 and 250 mg/kg of DRAE, respectively, by oral gavage for 28 days. All mice except from the negative control group were injected into the mammary fat pad with 4T1 cells (1 × 105 4T1 cells/0.1 mL of phosphate buffer solution). DRAE was administered orally on Day 11 after the tumor has developed. Results The tumor volume of the 1 000 mg/kg of DRAE group reduced significantly compared to the positive control while treatment with 500 mg/kg of DRAE had significantly inhibited metastasis to the heart. In the acute toxicity study, treatment with up to 5 000 mg/kg of DRAE was not toxic to the animals, indicating its safety when a large amount of this plant extract was ingested. Based on the sub-acute toxicity study, treatment of the highest dose of DRAE (1 000 mg/kg) had mild liver toxicity indicated by mild focal hemorrhage. Conclusions DRAE possesses anti-breast cancer properties but at the same time it shows mild toxicity to the liver. The non observable adverse effect dose for DRAE is 500 mg/kg.
first_indexed 2025-11-15T10:04:26Z
format Article
id upm-43781
institution Universiti Putra Malaysia
institution_category Local University
language English
last_indexed 2025-11-15T10:04:26Z
publishDate 2015
publisher Asian Pacific Journal of Tropical Biomedicine Editorial Office
recordtype eprints
repository_type Digital Repository
spelling upm-437812016-09-21T02:48:00Z http://psasir.upm.edu.my/id/eprint/43781/ Anti breast cancer properties and toxicity of Dillenia suffruticosa root aqueous extract in BALB/c mice Saiful Yazan, Latifah Yong, Sze Ong Zaaba, Nur Elena Mohd Ali, Razana Jhi, Biau Foo Yin, Sim Tor Objective To determine the anti-breast cancer activities and the safety oral consumption of Dillenia suffruticosa root aqueous extract (DRAE) in BALB/c mice. Methods In the anti-breast cancer study, female BALB/c mice were divided into five groups (n = 12), which were (1) positive control (with breast cancer, untreated), (2) negative control (without breast cancer, untreated) and other three groups of mice with breast cancer treated with 1 000, 500 and 250 mg/kg of DRAE, respectively, by oral gavage for 28 days. All mice except from the negative control group were injected into the mammary fat pad with 4T1 cells (1 × 105 4T1 cells/0.1 mL of phosphate buffer solution). DRAE was administered orally on Day 11 after the tumor has developed. Results The tumor volume of the 1 000 mg/kg of DRAE group reduced significantly compared to the positive control while treatment with 500 mg/kg of DRAE had significantly inhibited metastasis to the heart. In the acute toxicity study, treatment with up to 5 000 mg/kg of DRAE was not toxic to the animals, indicating its safety when a large amount of this plant extract was ingested. Based on the sub-acute toxicity study, treatment of the highest dose of DRAE (1 000 mg/kg) had mild liver toxicity indicated by mild focal hemorrhage. Conclusions DRAE possesses anti-breast cancer properties but at the same time it shows mild toxicity to the liver. The non observable adverse effect dose for DRAE is 500 mg/kg. Asian Pacific Journal of Tropical Biomedicine Editorial Office 2015 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/43781/1/1-s2.0-S2221169115002208-main.pdf Saiful Yazan, Latifah and Yong, Sze Ong and Zaaba, Nur Elena and Mohd Ali, Razana and Jhi, Biau Foo and Yin, Sim Tor (2015) Anti breast cancer properties and toxicity of Dillenia suffruticosa root aqueous extract in BALB/c mice. Asian Pacific Journal of Tropical Biomedicine, 5 (12). pp. 1018-1026. ISSN 2221-1691 http://www.elsevier.com/locate/apjtb 10.1016/j.apjtb.2015.09.008
spellingShingle Saiful Yazan, Latifah
Yong, Sze Ong
Zaaba, Nur Elena
Mohd Ali, Razana
Jhi, Biau Foo
Yin, Sim Tor
Anti breast cancer properties and toxicity of Dillenia suffruticosa root aqueous extract in BALB/c mice
title Anti breast cancer properties and toxicity of Dillenia suffruticosa root aqueous extract in BALB/c mice
title_full Anti breast cancer properties and toxicity of Dillenia suffruticosa root aqueous extract in BALB/c mice
title_fullStr Anti breast cancer properties and toxicity of Dillenia suffruticosa root aqueous extract in BALB/c mice
title_full_unstemmed Anti breast cancer properties and toxicity of Dillenia suffruticosa root aqueous extract in BALB/c mice
title_short Anti breast cancer properties and toxicity of Dillenia suffruticosa root aqueous extract in BALB/c mice
title_sort anti breast cancer properties and toxicity of dillenia suffruticosa root aqueous extract in balb/c mice
url http://psasir.upm.edu.my/id/eprint/43781/
http://psasir.upm.edu.my/id/eprint/43781/
http://psasir.upm.edu.my/id/eprint/43781/
http://psasir.upm.edu.my/id/eprint/43781/1/1-s2.0-S2221169115002208-main.pdf