Grzanka Dariusz, Gagat Maciej, Izdebska Magdalena, Marszałek Andrzej
Department and Clinic of Dermatology, Sexually Transmitted Diseases and Immunodermatology, Nicolaus Copernicus University in Toruń, Collegium Medicum in Bydgoszcz, 85-092 Bydgoszcz, Poland.
Department of Histology and Embryology, Nicolaus Copernicus University in Toruń, Collegium Medicum in Bydgoszcz, 85-092 Bydgoszcz, Poland.
Oncol Rep. 2015 Jan;33(1):250-66. doi: 10.3892/or.2014.3597. Epub 2014 Nov 11.
Cutaneous T-cell lymphoma (CTCL) is a group of slowly progressive, lymphoproliferative disorders characterized by localization of neoplastic T lymphocytes to the skin. The most common type of CTCL is mycosis fungoides which has a mild clinical course with slow and long progression. The rate of progression is generally slow and takes many years but often remains unpredictable. Special AT-rich sequence-binding protein-1 (SATB1) is a global chromatin organizer which controls gene expression by folding and remodeling chromatin, but which also regulates the level of histone methylation and acetylation, important in differentiation and apoptosis. The aim of the present study was to determine if SATB1 may be considered a prognostic and predictive factor of CTCL. The results showed that moderate and high expression of SATB1 correlate with significantly better prognosis of CTCL patients. Moreover, we showed that downregulation of SATB1 in Jurkat cells caused their resistance to activation-induced cell death. In conclusion, SATB1 expression appears to be a strong candidate as a prognostic factor confirming the inner heterogeneous features of CTCLs.
皮肤T细胞淋巴瘤(CTCL)是一组缓慢进展的淋巴增殖性疾病,其特征为肿瘤性T淋巴细胞定位于皮肤。CTCL最常见的类型是蕈样肉芽肿,其临床病程较轻,进展缓慢且病程长。进展速度通常较慢,需要数年时间,但往往仍不可预测。富含特殊AT序列结合蛋白1(SATB1)是一种全局染色质组织者,它通过折叠和重塑染色质来控制基因表达,但也调节组蛋白甲基化和乙酰化水平,这在分化和凋亡中很重要。本研究的目的是确定SATB1是否可被视为CTCL的预后和预测因素。结果表明,SATB1的中度和高表达与CTCL患者明显更好的预后相关。此外,我们表明Jurkat细胞中SATB1的下调导致其对激活诱导的细胞死亡产生抗性。总之,SATB1表达似乎是作为预后因素的有力候选者,证实了CTCL的内在异质性特征。