Modulation of cancer signalling pathway(s) in two-stage mouse skin tumorigenesis by annonacin

Background: Annonacin, an annonaceous acetogenin isolated from Annona muricata has been reported to be strongly cytotoxic against various cell lines, in vitro. Nevertheless, its effect against in vivo tumor promoting activity has not been reported yet. Therefore, this study was aimed to investigate...

Full description

Bibliographic Details
Main Authors: Md Roduan, Mohd Rohaizad, Abd Hamid @ Abdul Razak, Roslida, Mohtarrudin, Norhafizah
Format: Article
Language:English
Published: BioMed Central 2019
Online Access:http://psasir.upm.edu.my/id/eprint/81400/
http://psasir.upm.edu.my/id/eprint/81400/1/Modulation%20of%20cancer%20signalling%20pathway%28s%29%20in%20two-stage%20mouse%20skin%20tumorigenesis%20by%20annonacin.pdf
_version_ 1848859095510024192
author Md Roduan, Mohd Rohaizad
Abd Hamid @ Abdul Razak, Roslida
Mohtarrudin, Norhafizah
author_facet Md Roduan, Mohd Rohaizad
Abd Hamid @ Abdul Razak, Roslida
Mohtarrudin, Norhafizah
author_sort Md Roduan, Mohd Rohaizad
building UPM Institutional Repository
collection Online Access
description Background: Annonacin, an annonaceous acetogenin isolated from Annona muricata has been reported to be strongly cytotoxic against various cell lines, in vitro. Nevertheless, its effect against in vivo tumor promoting activity has not been reported yet. Therefore, this study was aimed to investigate antitumor-promoting activity of annonacin via in vivo two-stage mouse skin tumorigenesis model and its molecular pathways involved. Methods: Mice were initiated with single dose of 7,12-dimethylbenz[α]anthracene (DMBA) (390 nmol/100 μL) followed by, in subsequent week, repeated promotion (twice weekly; 22 weeks) with 12-O-tetradecanoylphorbol-13-acetate (TPA) (1.7 nmol/100 μL). Annonacin (85 nM) and curcumin (10 mg/kg; reference) were, respectively, applied topically to DMBA/TPA-induced mice 30 min before each TPA application for 22 weeks. Upon termination, histopathological examination of skin, liver and kidney as well as genes and proteins expression analysis were conducted to elucidate the potential mechanism of annonacin. Results: With comparison to the carcinogen control, Annonacin significantly increased the tumor latency period and reduced the tumor incidence, tumor burden and tumor volume, respectively. In addition, it also suppressed tumorigenesis manifested by significant reduction of hyperkeratosis, dermal papillae and number of keratin pearls on skin tissues. Annonacin also appeared to be non-toxic to liver and kidney. Significant modulation of both AKT, ERK, mTOR, p38, PTEN and Src genes and proteins were also observed in annonacin-targeted signaling pathway(s) against tumorigenesis. Conclusions: Collectively, results of this study indicate that annonacin is a potential therapeutic compound targeting tumor promoting stage in skin tumorigenesis by modulating multiple gene and protein in cancer signaling pathways without apparent toxicity.
first_indexed 2025-11-15T12:23:53Z
format Article
id upm-81400
institution Universiti Putra Malaysia
institution_category Local University
language English
last_indexed 2025-11-15T12:23:53Z
publishDate 2019
publisher BioMed Central
recordtype eprints
repository_type Digital Repository
spelling upm-814002021-01-31T17:40:06Z http://psasir.upm.edu.my/id/eprint/81400/ Modulation of cancer signalling pathway(s) in two-stage mouse skin tumorigenesis by annonacin Md Roduan, Mohd Rohaizad Abd Hamid @ Abdul Razak, Roslida Mohtarrudin, Norhafizah Background: Annonacin, an annonaceous acetogenin isolated from Annona muricata has been reported to be strongly cytotoxic against various cell lines, in vitro. Nevertheless, its effect against in vivo tumor promoting activity has not been reported yet. Therefore, this study was aimed to investigate antitumor-promoting activity of annonacin via in vivo two-stage mouse skin tumorigenesis model and its molecular pathways involved. Methods: Mice were initiated with single dose of 7,12-dimethylbenz[α]anthracene (DMBA) (390 nmol/100 μL) followed by, in subsequent week, repeated promotion (twice weekly; 22 weeks) with 12-O-tetradecanoylphorbol-13-acetate (TPA) (1.7 nmol/100 μL). Annonacin (85 nM) and curcumin (10 mg/kg; reference) were, respectively, applied topically to DMBA/TPA-induced mice 30 min before each TPA application for 22 weeks. Upon termination, histopathological examination of skin, liver and kidney as well as genes and proteins expression analysis were conducted to elucidate the potential mechanism of annonacin. Results: With comparison to the carcinogen control, Annonacin significantly increased the tumor latency period and reduced the tumor incidence, tumor burden and tumor volume, respectively. In addition, it also suppressed tumorigenesis manifested by significant reduction of hyperkeratosis, dermal papillae and number of keratin pearls on skin tissues. Annonacin also appeared to be non-toxic to liver and kidney. Significant modulation of both AKT, ERK, mTOR, p38, PTEN and Src genes and proteins were also observed in annonacin-targeted signaling pathway(s) against tumorigenesis. Conclusions: Collectively, results of this study indicate that annonacin is a potential therapeutic compound targeting tumor promoting stage in skin tumorigenesis by modulating multiple gene and protein in cancer signaling pathways without apparent toxicity. BioMed Central 2019 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/81400/1/Modulation%20of%20cancer%20signalling%20pathway%28s%29%20in%20two-stage%20mouse%20skin%20tumorigenesis%20by%20annonacin.pdf Md Roduan, Mohd Rohaizad and Abd Hamid @ Abdul Razak, Roslida and Mohtarrudin, Norhafizah (2019) Modulation of cancer signalling pathway(s) in two-stage mouse skin tumorigenesis by annonacin. BMC Complementary and Alternative Medicine, 19 (238). pp. 1-16. ISSN 1472-6882 https://bmccomplementmedtherapies.biomedcentral.com/articles/10.1186/s12906-019-2650-1 10.1186/s12906-019-2650-1
spellingShingle Md Roduan, Mohd Rohaizad
Abd Hamid @ Abdul Razak, Roslida
Mohtarrudin, Norhafizah
Modulation of cancer signalling pathway(s) in two-stage mouse skin tumorigenesis by annonacin
title Modulation of cancer signalling pathway(s) in two-stage mouse skin tumorigenesis by annonacin
title_full Modulation of cancer signalling pathway(s) in two-stage mouse skin tumorigenesis by annonacin
title_fullStr Modulation of cancer signalling pathway(s) in two-stage mouse skin tumorigenesis by annonacin
title_full_unstemmed Modulation of cancer signalling pathway(s) in two-stage mouse skin tumorigenesis by annonacin
title_short Modulation of cancer signalling pathway(s) in two-stage mouse skin tumorigenesis by annonacin
title_sort modulation of cancer signalling pathway(s) in two-stage mouse skin tumorigenesis by annonacin
url http://psasir.upm.edu.my/id/eprint/81400/
http://psasir.upm.edu.my/id/eprint/81400/
http://psasir.upm.edu.my/id/eprint/81400/
http://psasir.upm.edu.my/id/eprint/81400/1/Modulation%20of%20cancer%20signalling%20pathway%28s%29%20in%20two-stage%20mouse%20skin%20tumorigenesis%20by%20annonacin.pdf