卵巢癌中 297-11A 硫酸化聚糖的结构阐释和预后意义

IF 5.1 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Daisuke Inoue , Hitomi Hoshino , Ya-Ying Chen , Makoto Yamamoto , Akiya Kogami , Mana Fukushima , Kay-Hooi Khoo , Tomoya O. Akama , Yoshio Yoshida , Motohiro Kobayashi
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引用次数: 0

摘要

卵巢癌通常是在腹膜播散和/或淋巴结转移的晚期确诊的,这种晚期癌症的预后很差。因此,需要新的生物标志物来预测患者的预后。宫本(Miyamoto)等人之前研究发现,5D4 单克隆抗体检测到的硫酸角蛋白(KS)在卵巢癌中表达。然而,这种 KS 的详细结构尚未确定,这一发现的生物学意义仍有待澄清。我们之前生成了 297-11A 单克隆抗体,它能识别位于非还原末端的半乳糖(Gal)-6-O-硫酸化 N-乙酰半乳糖胺(LacNAc)。由于 297-11A 表位与 5D4 表位重叠,因此我们选择使用 297-11A 抗体作为分析 KS 及其相关结构的工具。我们用 297-11A 抗体结合一系列糖苷酶对 98 例卵巢癌病例进行了免疫组化分析,并对人类浆液性卵巢癌细胞系 OVCAR-3 进行了质谱分析,以推断 297-11A 硫酸化聚糖的聚糖结构。我们还进行了 Western 印迹分析,以评估 297-11A 硫酸化聚糖与粘蛋白核心蛋白粘蛋白 16(MUC16,又称癌症抗原 125 (CA125))的潜在关联。最后,我们研究了 297-11A 表达与患者预后之间的关系。结果发现,297-11A-硫酸化聚糖主要在浆液性癌和子宫内膜样癌中表达,而在粘液腺癌和透明细胞癌中表达较少。我们发现,从结构上看,卵巢癌中表达的 297-11A 硫酸化聚糖是携带部分硅烷基化、Gal-6-O 硫酸化 LacNAc 的 O 型聚糖,这些聚糖很可能显示在 MUC16 粘蛋白核心蛋白上。具有临床意义的是,297-11A-硫酸化聚糖的表达与患者较短的无进展生存期相关。因此,297-11A-硫酸化聚糖可作为卵巢癌复发的预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structural Elucidation and Prognostic Relevance of 297-11A-Sulfated Glycans in Ovarian Carcinoma

Ovarian carcinoma is usually diagnosed at an advanced stage with peritoneal dissemination and/or lymph node metastasis, and the prognosis for such advanced carcinoma is very poor. Therefore, new biomarkers to predict patient prognosis are needed. Miyamoto et al. previously showed that keratan sulfate (KS) detected by the 5D4 monoclonal antibody was expressed in ovarian carcinoma. However, the detailed structure of such KS was not determined, and the biological significance of this finding remained to be clarified. We previously generated the 297-11A monoclonal antibody, which recognizes galactose (Gal)-6-O-sulfated N-acetyllactosamine (LacNAc) located at the nonreducing terminus. Because the 297-11A epitope overlaps with that of 5D4, here we chose to use the 297-11A antibody as a tool to analyze KS and related structures. We conducted immunohistochemical analysis of 98 ovarian carcinoma cases with 297-11A antibody combined with a series of glycosidases and performed mass spectrometry analysis of the human serous ovarian carcinoma cell line OVCAR-3 to deduce the glycan structure of 297-11A-sulfated glycans. We also performed western blot analysis to assess a potential association of 297-11A-sulfated glycans with the mucin core protein mucin 16 (MUC16; also known as cancer antigen 125 (CA125)). Finally, we examined the relationship between 297-11A expression and patient prognosis. Consequently, 297-11A-sulfated glycans were primarily expressed in serous and endometrioid carcinomas and poorly expressed in mucinous and clear cell carcinomas. We reveal that structurally, 297-11A-sulfated glycans expressed in ovarian carcinoma are O-glycans carrying partially sialylated, Gal-6-O-sulfated LacNAc and that these glycans are likely displayed on MUC16 mucin core proteins. Of clinical importance is that expression of 297-11A-sulfated glycans correlated with shorter progression-free survival in patients. Thus, 297-11A-sulfated glycans may serve as a predictor of ovarian carcinoma recurrence.

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来源期刊
Laboratory Investigation
Laboratory Investigation 医学-病理学
CiteScore
8.30
自引率
0.00%
发文量
125
审稿时长
2 months
期刊介绍: Laboratory Investigation is an international journal owned by the United States and Canadian Academy of Pathology. Laboratory Investigation offers prompt publication of high-quality original research in all biomedical disciplines relating to the understanding of human disease and the application of new methods to the diagnosis of disease. Both human and experimental studies are welcome.
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