Mackrides Nicholas, Ganjei-Azar Parvin, Perez Roberto, Cui Tengijiao, Block Norman, Schally Andrew V, Nadji Mehrdad
Departments of Pathology and Medicine (N.M., P.G.-A., R.P., T.C., N.B., A.V.S., M.N.), Miller School of Medicine, Sylvester Comprehensive Cancer Center, University of Miami, Jackson Memorial Hospital VA Medical Center, Miami, Florida.
Int J Gynecol Pathol. 2016 Mar;35(2):142-6. doi: 10.1097/PGP.0000000000000229.
Malignant mixed Müllerian tumors (MMMTs) are aggressive malignant neoplasms with a high recurrence rate and poor prognosis. Despite advances in adjuvant therapies in recent years, the prognosis of these tumors has not improved. Growth hormone-releasing hormone (GHRH) is produced by a variety of malignant tumors and acts as a growth factor in an autocrine/paracrine manner. Its function requires the presence of its receptors to exert its effects on neoplastic cells. In this study, we evaluated the expression of GHRH receptors (GHRH-R) in a group of MMMTs. Thirty-one examples of MMMTs from endometrium, ovary, uterine tube, and pelvic peritoneum were retrieved from the files of Department of Pathology at the University of Miami, Jackson Memorial Hospital. Immunohistochemistry for GHRH-R was performed on paraffin sections and the staining results were evaluated separately in both epithelial and mesenchymal components of each tumor. The presence of pituitary type growth hormone-releasing hormone receptor mRNA and that of its biologically active splice variant were also evaluated by RT-PCR in 6 of the tumors. Positive immunohistochemical reaction for GHRH-R was detected in 30 tumors (96%). The epithelial and sarcomatous components were positive in 30 (96%), whereas one endometrial tumor was negative in both components. The mRNA for GHRH-R and its splice variant was found in all 6 tested tumors. This study shows that GHRH-R is expressed by the majority of MMMTs in both epithelial and mesenchymal components. This finding could potentially serve as a basis for therapeutic approaches using synthetic peptide antagonists of GHRH-R that have shown significant efficacy with minimal side effects in experimental models.
恶性苗勒管混合瘤(MMMTs)是侵袭性恶性肿瘤,复发率高且预后差。尽管近年来辅助治疗取得了进展,但这些肿瘤的预后并未改善。生长激素释放激素(GHRH)由多种恶性肿瘤产生,并以自分泌/旁分泌方式作为生长因子发挥作用。其功能需要其受体的存在才能对肿瘤细胞发挥作用。在本研究中,我们评估了一组MMMTs中生长激素释放激素受体(GHRH-R)的表达情况。从迈阿密大学杰克逊纪念医院病理学系的档案中检索到31例来自子宫内膜、卵巢、输卵管和盆腔腹膜的MMMTs。对石蜡切片进行GHRH-R免疫组织化学检测,并分别在每个肿瘤的上皮和间质成分中评估染色结果。还通过RT-PCR在6个肿瘤中评估了垂体型生长激素释放激素受体mRNA及其生物活性剪接变体的存在情况。在30个肿瘤(96%)中检测到GHRH-R的阳性免疫组织化学反应。上皮和肉瘤成分均为阳性的有30个(96%),而1例子宫内膜肿瘤的两个成分均为阴性。在所有6个检测的肿瘤中均发现了GHRH-R及其剪接变体的mRNA。本研究表明,大多数MMMTs的上皮和间质成分均表达GHRH-R。这一发现可能为使用GHRH-R合成肽拮抗剂的治疗方法提供基础,在实验模型中,这些拮抗剂已显示出显著疗效且副作用最小。