Department of Pathology, Antalya Training and Research Hospital, Antalya, Turkey.
Department of Pathology, Health Sciences University, Antalya Training and Research Hospital, Antalya, Turkey.
Ann Diagn Pathol. 2024 Oct;72:152330. doi: 10.1016/j.anndiagpath.2024.152330. Epub 2024 May 20.
Primary ovarian mucinous tumors are uncommon. Factors leading to invasive progression and metastatic disease have not been fully delineated yet. The aim of this study is to determine the rates of p53 and p16 immunoexpressions in primary ovarian mucinous tumors, to investigate their relationship with clinicopathologic factors and their impact on prognosis and survival.
Seventy-eight primary ovarian mucinous tumors (30 mucinous cystadenomas, 30 mucinous borderline tumors (MBOT), 18 mucinous carcinomas (MOC)) were evaluated immunohistochemically with p53 and p16 staining. The demographic, clinicopathological data, and postoperative follow-up findings of the patients were analyzed.
Mutation-type p53 staining was present in 1/30 (3.3 %) cystadenoma, 10/30 (33.3 %) MBOT and 9/18 (50 %) MOC (p = 0.001). p16 overexpression was detected in 3/30 (10.0 %) MBOT and 5/18 (27.8 %) MOC, but not in any cystadenoma (p = 0.04). The frequency of mutation-type p53 staining in MBOTs with microinvasion was higher (71.4 %) than in those without (28.6 %, p = 0.026). The frequencies of p16 or p53 mutations were similar in MBOTs with and without intraepithelial carcinoma, or mural nodule (p > 0.05). In MOCs with ovarian surface involvement, mutation-type p53 staining was detected in 66.7 % (6/9) and p16 overexpression in 55.6 % (5/9) of the cases. A significant difference was found between MOCs with or without ovarian surface involvement regarding the frequency of p16 overexpression (p = 0.029). Any relationship was not detected between survival and p53 and p16 expression in MOCs (p > 0.05).
p53 and p16 mutation rates were higher in MOCs compared to mucinous cystadenomas and MBOTs and suggest a relevant role in the development of primary ovarian mucinous carcinoma, however further studies are needed in this regard.
原发性卵巢黏液性肿瘤并不常见。导致侵袭性进展和转移性疾病的因素尚未完全阐明。本研究旨在确定原发性卵巢黏液性肿瘤中 p53 和 p16 免疫表达的发生率,探讨其与临床病理因素的关系及其对预后和生存的影响。
对 78 例原发性卵巢黏液性肿瘤(30 例黏液囊腺瘤、30 例交界性黏液性肿瘤(MBOT)、18 例黏液性癌(MOC))进行 p53 和 p16 免疫组化染色。分析患者的人口统计学、临床病理数据和术后随访结果。
30 例囊腺瘤中 1 例(3.3%)存在突变型 p53 染色,30 例 MBOT 中 10 例(33.3%)和 18 例 MOC 中 9 例(50%)存在突变型 p53 染色(p=0.001)。30 例 MBOT 中有 3 例(10.0%)和 18 例 MOC 中有 5 例(27.8%)存在 p16 过表达,但在任何囊腺瘤中均未发现(p=0.04)。MBOT 中存在微浸润时突变型 p53 染色的频率更高(71.4%),而不存在微浸润时的频率较低(28.6%,p=0.026)。MBOT 中存在上皮内癌或壁结节时,p16 或 p53 突变的频率相似(p>0.05)。在卵巢表面受累的 MOC 中,6 例(6/9)存在突变型 p53 染色,5 例(5/9)存在 p16 过表达。卵巢表面受累的 MOC 与无卵巢表面受累的 MOC 之间,p16 过表达的频率存在显著差异(p=0.029)。在 MOC 中,p53 和 p16 表达与生存之间未发现任何关系(p>0.05)。
与黏液囊腺瘤和 MBOT 相比,MOC 中 p53 和 p16 的突变率更高,提示其在原发性卵巢黏液性癌的发生发展中起重要作用,但这方面需要进一步研究。