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癌症/睾丸抗原表达对晚期多发性骨髓瘤患者的预后影响

Prognostic impact of cancer/testis antigen expression in advanced stage multiple myeloma patients.

作者信息

Andrade Valéria C C, Vettore André L, Felix Roberta S, Almeida Manuella S S, Carvalho Fabrício, Oliveira José Salvador R, Chauffaille Maria Lourdes Lopes Ferrari, Andriolo Adagmar, Caballero Otavia L, Zago Marco Antonio, Colleoni Gisele W B

机构信息

Discipline of Hematology and Hemotherapy, Universidade Federal de São Paulo, UNIFESP, São Paulo, Brazil.

出版信息

Cancer Immun. 2008 Feb 1;8:2.

Abstract

This study aims to analyze the expression of 14 cancer/testis (CT) antigens in multiple myeloma (MM) to identify possible prognostic markers and therapeutic targets. The expression of MAGEA1, MAGEA2, MAGEA3/6, MAGEA4, MAGEA10, MAGEA12, BAGE1, MAGEC1/CT7, the GAGE family, LAGE-1, PRAME, NY-ESO-1, SPA17 and SSX1 was studied by RT-PCR in 15 normal tissues, a pool of 10 normal bone marrow samples, 3 normal tonsils and bone marrow aspirates from 6 normal donors, 3 monoclonal gammopathies of undetermined significance (MGUS), 5 solitary plasmacytomas, 39 MM samples (95% advanced stage) and the MM cell line U266. MAGEC1/CT7 was expressed in bone marrow aspirates from one MGUS and one plasmacytoma. The frequencies at which CT antigen were found to be expressed in MM patients were MAGEC1/CT7 77%, LAGE-1 49%, MAGEA3/6 41%, MAGEA2 36%, GAGE family 33%, NY-ESO-1 33%, BAGE-1 28%, MAGEA1 26%, PRAME 23%, SSX-1 26%, MAGEA12 20.5%, MAGEA4 0%, and MAGEA10 0%. Cox's regression model showed that GAGE family expression and having >6 CT antigens expressed were independent prognostic factors when all patients were analyzed. However, MAGEC1/CT7 expression was the only independent prognostic factor when non-transplanted patients where analyzed. Based on our findings, MAGEC1/CT7, MAGEA3/6 and LAGE-1 are good candidates for immunotherapy, since together they cover 85% of our MM cases. Furthermore, expression of the GAGE family, >6 CT antigens and MAGEC1/CT7 seem to have impact on MM prognosis.

摘要

本研究旨在分析14种癌/睾丸(CT)抗原在多发性骨髓瘤(MM)中的表达,以确定可能的预后标志物和治疗靶点。通过逆转录聚合酶链反应(RT-PCR)研究了MAGEA1、MAGEA2、MAGEA3/6、MAGEA4、MAGEA10、MAGEA12、BAGE1、MAGEC1/CT7、GAGE家族、LAGE-1、PRAME、NY-ESO-1、SPA17和SSX1在15个正常组织、10份正常骨髓样本的混合样本、3个正常扁桃体以及6名正常供体的骨髓穿刺物、3例意义未明的单克隆丙种球蛋白病(MGUS)、5例孤立性浆细胞瘤、39份MM样本(95%为晚期)和MM细胞系U266中的表达情况。MAGEC1/CT7在1例MGUS和1例浆细胞瘤的骨髓穿刺物中表达。在MM患者中发现CT抗原表达的频率分别为:MAGEC1/CT7 77%、LAGE-1 49%、MAGEA3/6 41%、MAGEA2 36%、GAGE家族33%、NY-ESO-1 33%、BAGE-1 28%、MAGEA1 26%、PRAME 23%、SSX-1 26%、MAGEA12 20.5%、MAGEA4 0%、MAGEA10 0%。Cox回归模型显示,当分析所有患者时,GAGE家族表达以及有>6种CT抗原表达是独立的预后因素。然而,当分析未接受移植的患者时,MAGEC1/CT7表达是唯一的独立预后因素。基于我们的研究结果,MAGEC1/CT7、MAGEA3/6和LAGE-1是免疫治疗的良好候选对象,因为它们共同涵盖了我们85%的MM病例。此外,GAGE家族的表达、>6种CT抗原以及MAGEC1/CT7似乎对MM预后有影响。

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本文引用的文献

3
Initial therapy of multiple myeloma patients who are not candidates for stem cell transplantation.
Hematology Am Soc Hematol Educ Program. 2006:338-47. doi: 10.1182/asheducation-2006.1.338.
4
Active immunotherapy of multiple myeloma.
Eur J Cancer. 2006 Jul;42(11):1653-60. doi: 10.1016/j.ejca.2006.03.008. Epub 2006 Jun 22.
5
Quantifying and imaging NY-ESO-1/LAGE-1-derived epitopes on tumor cells using high affinity T cell receptors.
J Immunol. 2006 Jun 15;176(12):7308-16. doi: 10.4049/jimmunol.176.12.7308.
6
A new LAGE-1 peptide recognized by cytolytic T lymphocytes on HLA-A68 tumors.
Cancer Immunol Immunother. 2006 Jun;55(6):644-52. doi: 10.1007/s00262-005-0066-x. Epub 2005 Sep 27.
9
Cancer/testis antigens, gametogenesis and cancer.
Nat Rev Cancer. 2005 Aug;5(8):615-25. doi: 10.1038/nrc1669.
10
Promoter methylation of DAL-1/4.1B predicts poor prognosis in non-small cell lung cancer.
Clin Cancer Res. 2005 Apr 15;11(8):2954-61. doi: 10.1158/1078-0432.CCR-04-2206.

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