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后葡萄膜黑色素瘤的基因组研究。

Genomic investigations of posterior uveal melanoma.

作者信息

Hovland Peter G, Trempe Clement

机构信息

Schepens Retina Associates, Boston, MA 02215, USA.

出版信息

Semin Ophthalmol. 2005 Oct-Dec;20(4):231-8. doi: 10.1080/08820530500350522.

Abstract

The specific genetic mechanisms responsible for the malignant behavior of uveal melanoma are not known. Unlike cutaneous melanoma, epidemiologic studies have not demonstrated a definitive germline form of uveal melanoma, though familial melanoma and racial predilections occur. Molecular cytogenetic characterization of uveal melanoma suggests that somatic deletions of chromosome 3 are associated with a worse prognosis. Microarray technology has been used to characterize uveal melanoma gene expression and may provide tests useful for determining prognosis. As an improved understanding of the cellular mechanisms used by uveal melanoma is gained, new opportunities to adapt or design therapeutic approaches may emerge.

摘要

导致葡萄膜黑色素瘤恶性行为的具体遗传机制尚不清楚。与皮肤黑色素瘤不同,尽管存在家族性黑色素瘤和种族倾向,但流行病学研究尚未证实葡萄膜黑色素瘤有明确的种系形式。葡萄膜黑色素瘤的分子细胞遗传学特征表明,3号染色体的体细胞缺失与较差的预后相关。微阵列技术已被用于描述葡萄膜黑色素瘤的基因表达,可能会提供有助于判断预后的检测方法。随着对葡萄膜黑色素瘤所利用的细胞机制有了更深入的了解,调整或设计治疗方法可能会出现新的机会。

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