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蕈样肉芽肿和塞扎里综合征的分子发病机制。

The molecular pathogenesis of mycosis fungoides and Sézary syndrome.

作者信息

Döbbeling U

机构信息

Department of Dermatology, University Hospital Zurich, Zurich, Switzerland.

出版信息

G Ital Dermatol Venereol. 2008 Dec;143(6):385-94.

Abstract

Mycosis fungoides (MF) and the Sézary syndrome (Sz) are the two most frequent forms of cutaneous T cell lymphomas (CTCL). Generally the Sz is regarded as a leukemic variant of MF. They are caused by malignant CD4+ T cells, which infiltrate the skin and both diseases proceed in different stages. It has been found in colon carcinoma that cancerogenesis is a sequence of activation of different oncogenes and inactivation of tumor suppressor genes. This finding has initiated efforts to identify the genes that are responsible for the progression of MF and Sz. The development of new screening methods has strongly accelerated this search and many oncogenes and tumor suppressor genes have been identified that may play a role in the progression of both diseases. Changes in the expression of some of these genes are already found at early stages, whereas others become active or inactivated only in later stages. These results will help to search for more specific drugs and lead to a more exact staging that will help to develop effective and personalized treatments of these diseases.

摘要

蕈样肉芽肿(MF)和塞扎里综合征(Sz)是皮肤T细胞淋巴瘤(CTCL)最常见的两种形式。一般来说,Sz被认为是MF的白血病变体。它们由恶性CD4 + T细胞引起,这些细胞浸润皮肤,两种疾病都经历不同阶段。在结肠癌中发现,癌症发生是不同癌基因激活和肿瘤抑制基因失活的一系列过程。这一发现引发了人们对确定导致MF和Sz进展的基因的努力。新筛查方法的发展极大地加速了这一研究,已经确定了许多可能在两种疾病进展中起作用的癌基因和肿瘤抑制基因。其中一些基因的表达变化在早期就已发现,而其他基因仅在后期才变得活跃或失活。这些结果将有助于寻找更具特异性的药物,并导致更精确的分期,这将有助于开发针对这些疾病的有效和个性化治疗方法。

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