Yang Xiu Ying, Li Ying, Cai Song Qi, Wang Li, Qiang Jin Wei
Department of Radiology, Jinshan Hospital, Fudan University, Shanghai 201508, P.R. China.
Departments of Radiology, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.
Oncol Lett. 2021 Mar;21(3):206. doi: 10.3892/ol.2021.12467. Epub 2021 Jan 14.
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.
卵巢癌是女性生殖系统中第二常见的恶性肿瘤,也是癌症死亡的一个重要原因。早期卵巢癌的检测和诊断仍然是临床挑战,这就需要使用早期卵巢癌动物模型进行影像学研究。本研究旨在通过研究二甲基苯并蒽(DMBA)的给药方式、诱导剂量和暴露时间来优化DMBA诱导的大鼠卵巢肿瘤模型,并利用磁共振成像(MRI)探索肿瘤的形态学特征。共实施了三种方案。在方案一中,用装载高浓度液体DMBA的可吸收止血纱布覆盖卵巢。对于该方案,将150只Sprague-Dawley大鼠根据DMBA剂量(1.0、2.0和3.0毫克)分为三组。在方案二中,将DMBA溶液注射到卵巢包膜下。对于该方案,将159只大鼠分为0.5、1.0和1.5毫克DMBA组。在方案三中,用装载高浓度固体DMBA的可吸收纱布覆盖卵巢。对于该方案,将161只大鼠分为1.0、2.0和3.0毫克DMBA组。三种方案中的每组又进一步细分为60天、90天、120天、150天和180天组。在方案二中,肿瘤形成率为75.6%(99/131),其中1.5毫克组最高(86.4%,38/44),在第120天时达到100%(10/10)。诱导的肿瘤中93.9%(93/99)为浆液性。交界性卵巢肿瘤占所有肿瘤的19.2%(19/99),卵巢癌占46.5%(46/99)。交界性卵巢肿瘤的平均最大直径(MMD)为10.29±3.41毫米,卵巢癌为15.19±7.10毫米。随着恶性程度增加,实性成分的MMD增大。观察到囊性、囊实性和实性肿瘤。卵巢包膜下注射1.5毫克DMBA是大鼠卵巢肿瘤模型的最佳方案。该模型对于研究卵巢肿瘤的发生、发展和影像学表现是理想的。