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黑色素瘤抗原基因(MAGE)在眼黑色素瘤从原发性疾病进展为转移性疾病过程中的表达。

Expression of MAGE genes in ocular melanoma during progression from primary to metastatic disease.

作者信息

Chen P W, Murray T G, Uno T, Salgaller M L, Reddy R, Ksander B R

机构信息

The Schepens Eye Research Institute and The Department of Ophthalmology, Harvard Medical School, Boston, MA 02114, USA.

出版信息

Clin Exp Metastasis. 1997 Sep;15(5):509-18. doi: 10.1023/a:1018479011340.

Abstract

Primary melanomas that form within the eye have a unique pattern of disease progression as compared with melanomas that form within the skin. A high percentage of patients (approximately 50%) develop metastatic tumors that occur predominately in the liver. An unusual characteristic of ocular melanomas is the prolonged disease-free interval that extends for many years between the development of primary and metastatic tumors. It is estimated that the shortest interval between dissemination of tumor cells from the eye and the appearance of clinically detectable metastases is 6 years. A recent report indicated that fresh uveal melanoma tissue and metastatic tumor biopsies failed to express melanoma antigen gene (MAGE)-1, MAGE-2, or MAGE-3. In the present study, we examined the expression of MAGE genes on fresh and cultured tumor cells obtained from an ocular melanoma patient during different stages of progressive disease. MAGE gene expression was determined by reverse transcription-polymerase chain reaction using MAGE-1, MAGE-2 and MAGE-3 specific primers. Our results demonstrate that primary ocular tumor tissue and cultured tumor cells both express significant levels of MAGE-1, 2, and 3 at the time of enucleation. A high percentage of tumor cells within the primary tumor appear to express MAGE as demonstrated by consistent MAGE expression in 16 tumor cell clones. Metastatic liver tumors that developed 3 years after enucleation and 18 years after the initial formation of the primary tumor also expressed high levels of MAGE-1, -2, and -3. MAGE was expressed on fresh tumor tissue from a single biopsy and cultured tumor cells obtained from three of four different metastatic tumor nodules. When the MAGE-negative metastatic tumor cells were treated with the demethylating agent 5-Aza-2-Deoxycytidine (5-Aza-dC), transcription of MAGE-1 was restored, indicating the MAGE genes were not deleted. Our results demonstrate that in some patients, MAGE genes are expressed on primary and metastatic ocular melanomas.

摘要

与皮肤黑色素瘤相比,眼部原发性黑色素瘤具有独特的疾病进展模式。高比例的患者(约50%)会发生转移性肿瘤,主要发生在肝脏。眼部黑色素瘤的一个不寻常特征是,原发性和转移性肿瘤发生之间存在长达数年的无病间期延长。据估计,肿瘤细胞从眼部播散到临床可检测到转移灶出现的最短间隔为6年。最近一份报告指出,新鲜葡萄膜黑色素瘤组织和转移性肿瘤活检标本未能表达黑色素瘤抗原基因(MAGE)-1、MAGE-2或MAGE-3。在本研究中,我们检测了从一名眼部黑色素瘤患者在疾病进展不同阶段获取的新鲜和培养肿瘤细胞上MAGE基因的表达。使用MAGE-1、MAGE-2和MAGE-3特异性引物,通过逆转录-聚合酶链反应测定MAGE基因表达。我们的结果表明,原发性眼部肿瘤组织和培养的肿瘤细胞在眼球摘除时均表达显著水平的MAGE-1、2和3。原发性肿瘤内高比例的肿瘤细胞似乎表达MAGE,16个肿瘤细胞克隆中MAGE表达一致证明了这一点。在眼球摘除3年后以及原发性肿瘤最初形成18年后发生的转移性肝肿瘤也表达高水平的MAGE-1、-2和-3。MAGE在单次活检的新鲜肿瘤组织以及从四个不同转移性肿瘤结节中的三个获取的培养肿瘤细胞上表达。当用去甲基化剂5-氮杂-2'-脱氧胞苷(5-aza-dC)处理MAGE阴性的转移性肿瘤细胞时,MAGE-1的转录得以恢复,表明MAGE基因未缺失。我们的结果表明,在一些患者中,MAGE基因在原发性和转移性眼部黑色素瘤上表达。

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