在去势抵抗性前列腺癌中,MUC1表达与ST3GAL2相关,且与雄激素受体负相关。

IF 2.7 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Glycoconjugate Journal Pub Date : 2024-12-01 Epub Date: 2024-12-24 DOI:10.1007/s10719-024-10173-8
Shotaro Nakanishi, Tetsuji Suda, Kei Tanaka, Tomoko Yonamine, Kenji Numahata, Ai Sugawa, Takuma Oshiro, Yoshinori Oshiro, Seiichi Saito, Junichi Inokuchi
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引用次数: 0

摘要

阶段特异性胚胎抗原-4 (Stage-specific embryonic antigen-4, SSEA-4)是一种受发育调控的抗原,在多种恶性肿瘤中,SSEA-4和/或其合成酶ST3GAL2的表达水平与预后相关。我们报道了SSEA-4在去势抵抗性前列腺癌(CRPC)中显著升高,并与雄激素受体(AR)呈负相关。同时,随着越来越多地使用雄激素受体信号抑制剂治疗转移性CRPC (mCRPC), AR的损失增加到约30%。然而,监测ar阴性前列腺癌的进展状态是一个挑战,因为它不产生前列腺特异性抗原。基于AR与SSEA-4表达的负相关关系,我们假设一个与SSEA-4表达同步的可溶性分子可能是AR阴性前列腺癌的血清标志物候选物。因此,我们研究了st3gal2敲除DU145细胞中SSEA-4表达的分子背景。本研究表明MUC1被鉴定为与ST3GAL2相关的分子,并在ar阴性前列腺癌中表达。在前列腺癌细胞系和CRPC组织中,AR与MUC1的表达呈负相关。在CRPC组织中ar阴性前列腺癌细胞中MUC1的平均表达率接近60%。血清CA15-3 (MUC1)水平在mCRPC各分期中最高,其水平越高,mCRPC进展越快。我们的研究结果表明MUC1被鉴定为st3gal2相关分子,并在ar阴性的CRPC细胞中表达。此外,血清CA15-3水平可能反映mCRPC的进展情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MUC1 expression is associated with ST3GAL2 and negatively correlated with the androgen receptor in castration-resistant prostate cancer.

Stage-specific embryonic antigen-4 (SSEA-4) is a developmentally regulated antigen, while expression level of SSEA-4 and / or its synthase ST3GAL2 is associated with prognosis in various malignancies. We have reported a prominent increase of SSEA-4 in castration-resistant prostate cancer (CRPC) and its negative correlation with the androgen receptor (AR). Meanwhile, loss of AR has increased to approximately 30% with the growing use of androgen receptor signaling inhibitor for metastatic CRPC (mCRPC). However, monitoring the progression status of AR-negative prostate cancer is a challenge because it does not produce prostate-specific antigen. Based on the negative relationship of expression between AR and SSEA-4, we hypothesized that a soluble molecule synchronized with SSEA-4 in expression could be a serum marker candidate for AR-negative prostate cancer. Thus, we investigated the molecular background of SSEA-4 expression by ST3GAL2-knockout in DU145 cells. Here we show that MUC1 is identified as a molecule associated with ST3GAL2 and expressed in AR-negative prostate cancer. A negative correlation of expression between AR and MUC1 was observed in prostate cancer cell lines and CRPC tissues. The average rate of MUC1 expression was nearly 60% in AR-negative prostate cancer cells in CRPC tissues. Level of serum CA15-3 (MUC1) was the highest in mCRPC among various stages and its higher level was associated with faster progression of mCRPC. Our results demonstrate that MUC1 is identified as a ST3GAL2-associated molecule and expressed in AR-negative CRPC cells. Furthermore, level of serum CA15-3 may reflect the progression status of mCRPC.

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来源期刊
Glycoconjugate Journal
Glycoconjugate Journal 生物-生化与分子生物学
CiteScore
6.00
自引率
3.30%
发文量
63
审稿时长
1 months
期刊介绍: Glycoconjugate Journal publishes articles and reviews on all areas concerned with: function, composition, structure, biosynthesis, degradation, interactions, recognition and chemo-enzymatic synthesis of glycoconjugates (glycoproteins, glycolipids, oligosaccharides, polysaccharides and proteoglycans), biochemistry, molecular biology, biotechnology, immunology and cell biology of glycoconjugates, aspects related to disease processes (immunological, inflammatory, arthritic infections, metabolic disorders, malignancy, neurological disorders), structural and functional glycomics, glycoimmunology, glycovaccines, organic synthesis of glycoconjugates and the development of methodologies if biologically relevant, glycosylation changes in disease if focused on either the discovery of a novel disease marker or the improved understanding of some basic pathological mechanism, articles on the effects of toxicological agents (alcohol, tobacco, narcotics, environmental agents) on glycosylation, and the use of glycotherapeutics. Glycoconjugate Journal is the official journal of the International Glycoconjugate Organization, which is responsible for organizing the biennial International Symposia on Glycoconjugates.
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