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Optimization of 7,12-dimethylbenz(a)anthracene-induced rat epithelial ovarian tumors
Ovarian carcinoma is the second most common malignant tumor of the female reproductive system and an notable cause of cancer death. The detection and diagnosis of early ovarian carcinomas are still clinical challenges, which calls for imaging studies using early ovarian carcinoma animal models. The...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816358/ https://www.ncbi.nlm.nih.gov/pubmed/33574945 http://dx.doi.org/10.3892/ol.2021.12467 |
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author | Yang, Xiu Ying Li, Ying Cai, Song Qi Wang, Li Qiang, Jin Wei |
author_facet | Yang, Xiu Ying Li, Ying Cai, Song Qi Wang, Li Qiang, Jin Wei |
author_sort | Yang, Xiu Ying |
collection | PubMed |
description | Ovarian carcinoma is the second most common malignant tumor of the female reproductive system and an notable cause of cancer death. The detection and diagnosis of early ovarian carcinomas are still clinical challenges, which calls for imaging studies using early ovarian carcinoma animal models. The present study aimed to optimize the 7,12-dimethylbenz(a)anthracene (DMBA)-induced model of rat ovarian tumors by investigating the delivery methods, induction dose and time of DMBA exposure, and explored the morphological features of tumors using MRI. Three schemes were performed. In scheme one the ovary was covered with absorbable hemostatic gauze loaded with a high concentration of liquid DMBA. For this scheme, 150 Sprague-Dawley rats were divided into three groups depending on the DMBA dose (1.0, 2.0 and 3.0 mg). In scheme two DMBA solution was injected under the ovarian capsule. For this scheme, 159 rats were divided into 0.5, 1.0 and 1.5 mg DMBA groups. In scheme three the ovary was covered with absorbable gauze loaded with a high concentration of solid DMBA. For this scheme 161 rats were divided into 1.0, 2.0 and 3.0 mg DMBA groups. Each group of the three schemes was further subdivided into 60-, 90-, 120-, 150- and 180-day groups. In scheme two, the tumor formation rate was 75.6% (99/131), which was the highest in the 1.5 mg group (86.4%, 38/44) and reached 100% (10/10) on day 120. The induced tumors were serous in 93.9% (93/99) of tumors. Borderline ovarian tumors accounted for 19.2% (19/99) of all tumors, and ovarian cancer accounted for 46.5% (46/99). The mean maximum diameter (MMD) of borderline ovarian tumors was 10.29±3.41 mm, and that of ovarian cancer was 15.19±7.10 mm. MMD of the solid components increased with increasing malignancy. Cystic, cystic-solid and solid tumors were observed. The ovarian subcapsular injection of 1.5 mg DMBA was the best scheme for the rat ovarian tumor model. The present model is ideal for investigating the occurrence, development and imaging of ovarian tumors. |
format | Online Article Text |
id | pubmed-7816358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-78163582021-02-10 Optimization of 7,12-dimethylbenz(a)anthracene-induced rat epithelial ovarian tumors Yang, Xiu Ying Li, Ying Cai, Song Qi Wang, Li Qiang, Jin Wei Oncol Lett Articles Ovarian carcinoma is the second most common malignant tumor of the female reproductive system and an notable cause of cancer death. The detection and diagnosis of early ovarian carcinomas are still clinical challenges, which calls for imaging studies using early ovarian carcinoma animal models. The present study aimed to optimize the 7,12-dimethylbenz(a)anthracene (DMBA)-induced model of rat ovarian tumors by investigating the delivery methods, induction dose and time of DMBA exposure, and explored the morphological features of tumors using MRI. Three schemes were performed. In scheme one the ovary was covered with absorbable hemostatic gauze loaded with a high concentration of liquid DMBA. For this scheme, 150 Sprague-Dawley rats were divided into three groups depending on the DMBA dose (1.0, 2.0 and 3.0 mg). In scheme two DMBA solution was injected under the ovarian capsule. For this scheme, 159 rats were divided into 0.5, 1.0 and 1.5 mg DMBA groups. In scheme three the ovary was covered with absorbable gauze loaded with a high concentration of solid DMBA. For this scheme 161 rats were divided into 1.0, 2.0 and 3.0 mg DMBA groups. Each group of the three schemes was further subdivided into 60-, 90-, 120-, 150- and 180-day groups. In scheme two, the tumor formation rate was 75.6% (99/131), which was the highest in the 1.5 mg group (86.4%, 38/44) and reached 100% (10/10) on day 120. The induced tumors were serous in 93.9% (93/99) of tumors. Borderline ovarian tumors accounted for 19.2% (19/99) of all tumors, and ovarian cancer accounted for 46.5% (46/99). The mean maximum diameter (MMD) of borderline ovarian tumors was 10.29±3.41 mm, and that of ovarian cancer was 15.19±7.10 mm. MMD of the solid components increased with increasing malignancy. Cystic, cystic-solid and solid tumors were observed. The ovarian subcapsular injection of 1.5 mg DMBA was the best scheme for the rat ovarian tumor model. The present model is ideal for investigating the occurrence, development and imaging of ovarian tumors. D.A. Spandidos 2021-03 2021-01-14 /pmc/articles/PMC7816358/ /pubmed/33574945 http://dx.doi.org/10.3892/ol.2021.12467 Text en Copyright: © Yang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Yang, Xiu Ying Li, Ying Cai, Song Qi Wang, Li Qiang, Jin Wei Optimization of 7,12-dimethylbenz(a)anthracene-induced rat epithelial ovarian tumors |
title | Optimization of 7,12-dimethylbenz(a)anthracene-induced rat epithelial ovarian tumors |
title_full | Optimization of 7,12-dimethylbenz(a)anthracene-induced rat epithelial ovarian tumors |
title_fullStr | Optimization of 7,12-dimethylbenz(a)anthracene-induced rat epithelial ovarian tumors |
title_full_unstemmed | Optimization of 7,12-dimethylbenz(a)anthracene-induced rat epithelial ovarian tumors |
title_short | Optimization of 7,12-dimethylbenz(a)anthracene-induced rat epithelial ovarian tumors |
title_sort | optimization of 7,12-dimethylbenz(a)anthracene-induced rat epithelial ovarian tumors |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816358/ https://www.ncbi.nlm.nih.gov/pubmed/33574945 http://dx.doi.org/10.3892/ol.2021.12467 |
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