CD44s异构体是预测儿童颅咽管瘤复发的潜在生物标记物

IF 3.3 4区 医学 Q2 NEUROSCIENCES NeuroMolecular Medicine Pub Date : 2024-07-17 DOI:10.1007/s12017-024-08797-y
K Bajdak-Rusinek, N Diak, E Gutmajster, A Fus-Kujawa, M Ciupińska, B Kalina-Faska, A Trybus, M Grajek, M Kalina, M Mandera
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引用次数: 0

摘要

金刚瘤性颅咽管瘤(ACP)是一种颅内肿瘤,因其具有浸润周围结构的能力和根治性切除后仍易复发的倾向而被认为是部分恶性肿瘤。CD44 是 ACP 中已知的干细胞标志物,在 ACP 侵袭性突起的细胞簇中上调;然而,CD44s 和 CD44v1-10 这两种替代剪接异构体在 ACP 复发方面的功能尚未得到研究,尽管它们在癌症发展和进展中的作用已得到证实。在本研究中,我们首次证实了复发患者样本与未复发患者样本中 CD44 总表达量的差异。此外,我们的研究结果表明,在复发样本中,主要表达的同工酶是 CD44s,这可能表明它在预测 ACP 复发方面具有重要意义。CD44 表达增加与复发之间的关联可能会导致开发出 ACP 侵袭性和复发可能性的预后标志物;然而,CD44 表达的确切机制还需要进一步的研究来阐明。
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The CD44s Isoform is a Potential Biomarker for Predicting Craniopharyngioma Recurrence in Children.

Adamantinomatous craniopharyngioma (ACP) is an intracranial tumor considered partly malignant due to its ability to infiltrate surrounding structures and tendency to relapse despite radical resection. CD44 is a known stem cell marker in ACP and is upregulated in cell clusters of invasive ACP protrusions; however, the functions of its alternative splicing isoform variants, CD44s and CD44v1-10, have not yet been studied in terms of ACP recurrence, despite their confirmed roles in cancer development and progression. In this study, we first confirmed the difference in total CD44 expression between samples from patients who experienced relapse and those from patients who did not. Moreover, our findings showed that, in recurrent samples, the predominant isoform expressed was CD44s, which might indicate its significance in predicting ACP recurrence. The association between increased CD44 expression and recurrence may lead to the development of prognostic markers of ACP aggressiveness and relapse potential; however, further studies are needed to clarify the exact mechanism of CD44 expression.

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来源期刊
NeuroMolecular Medicine
NeuroMolecular Medicine 医学-神经科学
CiteScore
7.10
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: NeuroMolecular Medicine publishes cutting-edge original research articles and critical reviews on the molecular and biochemical basis of neurological disorders. Studies range from genetic analyses of human populations to animal and cell culture models of neurological disorders. Emerging findings concerning the identification of genetic aberrancies and their pathogenic mechanisms at the molecular and cellular levels will be included. Also covered are experimental analyses of molecular cascades involved in the development and adult plasticity of the nervous system, in neurological dysfunction, and in neuronal degeneration and repair. NeuroMolecular Medicine encompasses basic research in the fields of molecular genetics, signal transduction, plasticity, and cell death. The information published in NEMM will provide a window into the future of molecular medicine for the nervous system.
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