Hesa-A improves clinical outcome of oral carcinoma by affecting p53 gene expression in vivo
dc.contributor.author | Abbasi, MM | |
dc.contributor.author | Helli, S | |
dc.contributor.author | Monfaredan, A | |
dc.contributor.author | Jahanban-Esfahlan, R | |
dc.date.accessioned | 2018-08-26T08:56:47Z | |
dc.date.available | 2018-08-26T08:56:47Z | |
dc.date.issued | 2015 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54490 | |
dc.description.abstract | Background: Oral carcinoma (OC) remains as one of the most difficult malignancies to cure. Hesa-A is an Iranian herbal-marine compound that has shown promising anti-tumor properties on various human cancer cells, although the mechanisms of action remain to be addressed. This study was conducted to evaluate the effect of two doses of Hesa-A on mRNA expression of p53 as a main prognosticator of OC. Materials and Methods: 60 rats were randomly divided into 5 groups of 12 animals each. Rats in carcinoma groups received 0, 250 and 500 mg/kg body weight of Hesa-A three times a day. The two other groups considered as treated and untreated healthy groups. At the end of experiment, animals were sacrificed and tongue tissues subjected to H and E staining and real time PCR. Results: Our results indicated that compared to healthy group, p53 over expressed ~ 40% in untreated carcinoma group. After treatment with 250mg/kg and 500mg/kg body weights of Hesa-A , p53 level dropped by 53.4% and 13.6 %, respectively, compared to untreated carcinoma group (p<0.05, p<0.0001). Moreover, there was a significant relation between p53 mRNA content and observed pathological changes in studied groups (p<0.05). Conclusions: These data provide insights into the mechanism(s) by which Hesa-A improves clinical outcome of oral carcinoma by modulation of p53 expression. | |
dc.language.iso | English | |
dc.relation.ispartof | Asian Pacific Journal of Cancer Prevention | |
dc.subject | 4 nitroquinoline 1 oxide | |
dc.subject | HESA-A preparation | |
dc.subject | messenger RNA | |
dc.subject | plant medicinal product | |
dc.subject | animal | |
dc.subject | carcinoma | |
dc.subject | chemically induced | |
dc.subject | drug effects | |
dc.subject | gene expression | |
dc.subject | genetics | |
dc.subject | male | |
dc.subject | metabolism | |
dc.subject | pathology | |
dc.subject | phytotherapy | |
dc.subject | randomization | |
dc.subject | rat | |
dc.subject | Sprague Dawley rat | |
dc.subject | Tongue Neoplasms | |
dc.subject | tumor suppressor gene | |
dc.subject | 4-Nitroquinoline-1-oxide | |
dc.subject | Animals | |
dc.subject | Carcinoma | |
dc.subject | Gene Expression | |
dc.subject | Genes, p53 | |
dc.subject | Male | |
dc.subject | Phytotherapy | |
dc.subject | Plant Preparations | |
dc.subject | Random Allocation | |
dc.subject | Rats | |
dc.subject | Rats, Sprague-Dawley | |
dc.subject | RNA, Messenger | |
dc.subject | Tongue Neoplasms | |
dc.title | Hesa-A improves clinical outcome of oral carcinoma by affecting p53 gene expression in vivo | |
dc.type | Article | |
dc.citation.volume | 16 | |
dc.citation.issue | 10 | |
dc.citation.spage | 4169 | |
dc.citation.epage | 4172 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.7314/APJCP.2015.16.10.4169 |