| dc.date.accessioned | 1399-07-08T18:08:09Z | fa_IR |
| dc.date.accessioned | 2020-09-29T18:08:09Z | |
| dc.date.available | 1399-07-08T18:08:09Z | fa_IR |
| dc.date.available | 2020-09-29T18:08:09Z | |
| dc.date.issued | 2015-10-01 | en_US |
| dc.date.issued | 1394-07-09 | fa_IR |
| dc.identifier.citation | (2015). Hesa-A Improves Clinical Outcome of Oral Carcinoma by Affecting p53 Gene Expression in vivo. Asian Pacific Journal of Cancer Prevention, 16(10), 4169-4172. | en_US |
| dc.identifier.issn | 1513-7368 | |
| dc.identifier.issn | 2476-762X | |
| dc.identifier.uri | http://journal.waocp.org/article_31061.html | |
| dc.identifier.uri | https://iranjournals.nlai.ir/handle/123456789/37025 | |
| dc.description.abstract | <b>Background:</b> Oral carcinoma (OC) remains as one of the most difficult malignancies to cure. Hesa-A is anIranian herbal-marine compound that has shown promising anti-tumor properties on various human cancercells, although the mechanisms of action remain to be addressed. This study was conducted to evaluate the effectof two doses of Hesa-A on mRNA expression of p53 as a main prognosticator of OC. Materials and <br/><b>Methods</b>:60 rats were randomly divided into 5 groups of 12 animals each. Rats in carcinoma groups received 0, 250 and500 mg/kg body weight of Hesa-A three times a day. The two other groups considered as treated and untreatedhealthy groups. At the end of experiment, animals were sacrificed and tongue tissues subjected to H and Estaining and real time PCR. <br/><b>Results</b>: 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 , p53level 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 instudied groups (p<0.05). <br/><b>Conclusions</b>: These data provide insights into the mechanism(s) by which Hesa-Aimproves clinical outcome of oral carcinoma by modulation of p53 expression. | en_US |
| dc.format.extent | 497 | |
| dc.format.mimetype | application/pdf | |
| dc.language | English | |
| dc.language.iso | en_US | |
| dc.publisher | West Asia Organization for Cancer Prevention (WAOCP) | en_US |
| dc.relation.ispartof | Asian Pacific Journal of Cancer Prevention | en_US |
| dc.subject | HESA-A | en_US |
| dc.subject | oral carcinoma | en_US |
| dc.subject | p53 expression | en_US |
| dc.subject | clinical outcome | en_US |
| dc.subject | rat model | en_US |
| dc.subject | oral doses | en_US |
| dc.title | Hesa-A Improves Clinical Outcome of Oral Carcinoma by Affecting p53 Gene Expression in vivo | en_US |
| dc.type | Text | en_US |
| dc.citation.volume | 16 | |
| dc.citation.issue | 10 | |
| dc.citation.spage | 4169 | |
| dc.citation.epage | 4172 | |