Literature DB >> 23174723

Anti-tumor effect of Ardisia crispa hexane fraction on 7, 12-dimethylbenz[α]anthracene-induced mouse skin papillomagenesis.

Hamizah Sulaiman1, Roslida Abdul Hamid, Yeong Looi Ting, Fezah Othman.   

Abstract

CONTEXT: Ardisia crispa Thunb. A. DC (Myrsinaceae) or locally known as hen's eyes has been used in local folk medicine as a remedy in various illnesses. Previously, it has been reported to inhibit various inflammatory diseases. However, research done on this plant is still limited. AIMS: In the present study, the hexane fraction of the A. crispa root (ACRH) was evaluated on the peri-initiation and promotion phases of skin carcinogenesis.
MATERIALS AND METHODS: This two-stage skin carcinogenesis was induced by a single topical application of 7,12-dimethylbenz(α)anthracene (DMBA) and promoted by repeated treatment with croton oil for 10 weeks in Imprinting Control Region (ICR) mice. Morphological observation would be conducted to measure tumor incidence, tumor burden, and tumor volume. Histological evaluation on the skin tissue would also be done.
RESULTS: The carcinogen control group exhibited 66.67% of tumor incidence. Although, in the ACRH-treated groups, at 30 mg/kg, the mice showed only 10% of tumor incidence with a significant reduction (P < 0.05) in the values of tumor burden and tumor volume of 2.00 and 0.52 mm(3), respectively. Furthermore, the result was significantly lower than that of the carcinogen and curcumin control. At 100 mg/kg, ACRH showed a comparable result to carcinogen control. On the contrary, at 300 mg/kg, ACRH exhibited 100% tumor incidence and showed a significant elevated (P < 0.05) value of tumor burden (3.80) and tumor volume (14.67 ± 2.48 mm(3)).
CONCLUSIONS: The present study thus demonstrates that the anti-tumor effect of the chemopreventive potential of ACRH is at a lower dosage (30 mg/kg bwt) in both the initiating and promotion period, yet it exhibits a promoting effect at a higher dosage (300 mg/kg bwt).

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Year:  2012        PMID: 23174723     DOI: 10.4103/0973-1482.103521

Source DB:  PubMed          Journal:  J Cancer Res Ther        ISSN: 1998-4138            Impact factor:   1.805


  4 in total

1.  Cytotoxicity and Apoptosis Induction of Ardisia crispa and Its Solvent Partitions against Mus musculus Mammary Carcinoma Cell Line (4T1).

Authors:  Muhammad Luqman Nordin; Arifah Abdul Kadir; Zainul Amiruddin Zakaria; Fauziah Othman; Rasedee Abdullah; Muhammad Nazrul Hakim Abdullah
Journal:  Evid Based Complement Alternat Med       Date:  2017-03-16       Impact factor: 2.629

2.  Cytotoxic 13,28 Epoxy Bridged Oleanane-Type Triterpenoid Saponins from the Roots of Ardisia crispa.

Authors:  Xin Yin; Ruihang Hu; Yongqiang Zhou; Weiqian Zhu; Ying Zhou
Journal:  Molecules       Date:  2022-02-04       Impact factor: 4.411

3.  Integrated transcriptome and metabolome analyses revealed regulatory mechanisms of flavonoid biosynthesis in Radix Ardisia.

Authors:  Chang Liu; Jie Pan; Zhi-Gang Yin; Tingting Feng; Jiehong Zhao; Xiu Dong; Ying Zhou
Journal:  PeerJ       Date:  2022-06-29       Impact factor: 3.061

4.  Low dose triterpene-quinone fraction from Ardisia crispa root precludes chemical-induced mouse skin tumor promotion.

Authors:  Looi Ting Yeong; Roslida Abdul Hamid; Latifah Saiful Yazan; Huzwah Khaza'ai; Norhafizah Mohtarrudin
Journal:  BMC Complement Altern Med       Date:  2015-12-05       Impact factor: 3.659

  4 in total

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