2016
DOI: 10.1016/j.archoralbio.2016.06.015
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Chemopreventive effect of Toona sinensis leaf extract on 7,12-dimethylbenz[a]anthracene-induced hamster buccal pouch squamous cell carcinogenesis

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Cited by 10 publications
(5 citation statements)
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“…In the current study, the duration of DMBA application was carefully planned according to the previous literatures, at 8 weeks for the animals of GII A in order to achieve development of intact epithelial dysplasia, but not invasive SCC, and at 14 weeks for the animals of GII B in order to achieve development of invasive OSCC (16,17) . In the present study, the chemopreventive agent has been administered one week before and during carcinogen administration following the protocol of previous studies (18,19) .…”
Section: Discussionmentioning
confidence: 99%
“…In the current study, the duration of DMBA application was carefully planned according to the previous literatures, at 8 weeks for the animals of GII A in order to achieve development of intact epithelial dysplasia, but not invasive SCC, and at 14 weeks for the animals of GII B in order to achieve development of invasive OSCC (16,17) . In the present study, the chemopreventive agent has been administered one week before and during carcinogen administration following the protocol of previous studies (18,19) .…”
Section: Discussionmentioning
confidence: 99%
“…In addition, TSL aqueous extracts can inhibit the proliferation and induce the apoptosis of hamster cheek pouch squamous cell carcinoma induced by 7,12-dimethylbenz[a]anthracene (DMBA). Downregulation of the protein expression of survivin, X chromosome-linked inhibitor of apoptosis (XIAP), proliferating cell nuclear antigen (PCNA), iNOS and COX-2 and increased apoptotic activity suggested that TSL therapy might aid the prevention of oral cancer [86].…”
Section: Antitumor Activitymentioning
confidence: 99%
“…In vivo studies with nobiletin on male BALB/c nude mice suppressed tumor formation and metastasis by downregulating NF-κB translocation, MMP-2, and TIMP-2 proteins, and decreased phosphorylation of ERK1/2 ( Chien et al, 2015 ). Toona sinensis crude extract decreased the incidences of SCCs, tumor number, tumor volume, and tumor burden in male Syrian golden hamsters by downregulating protein levels of survivin, XIAP, PCNA, iNOS, and COX-2 ( Wang et al, 2016 ). Delayed tumor initiation incidence was reported in bitter melon extract–fed mice ( Sur et al, 2018 ).…”
Section: Head and Neck Cancer Spectrummentioning
confidence: 99%