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Molecular markers(PECAM-1,ICAM-3,HLA-DR)determine prognosis in primary non-Hodgkin's gastric lymphoma patients 被引量:4

Molecular markers(PECAM-1,ICAM-3,HLA-DR)determine prognosis in primary non-Hodgkin's gastric lymphoma patients
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摘要 AIM: To investigate the prognostic significance of PECAM-1, ICAM-3 and HLA-DR antigens in patients with primary non-Hodgkin's gastric lymphoma. METHODS: We immunohistochemically studied PECAM-1, ICAM-3 and HLA-DR antigen expression in 36 B-cell MALT-type primary gastric lymphoma patients. Ten non-malignant and ten healthy gastric tissue specimens were used as controls. Clinicopathological and survival data were correlated with the staining results. RESULTS: HLA-DR antigen expression was detected in 33 gastric lymphoma patients (91.7%) and 6 nonmalignant patients (54.5%). PECAM-1 stained tumor cells of 10 patients (27.8%), endothelial cells of 9 patients (25%) and inflammatory infiltrate of 4 patients (40%) with benign gastric disease. ICAM-3 expression was observed on the tumor cells of 17 patients (47.2%), while 5 non-malignant patients (50%) were stained positive as well. None of the healthy controls was stained for any of the genes studied. In the multivariate analysis, HLA-DR antigen and PECAM-1 were proved to be statistically significant independent prognostic factors associated with a favourable and an unfavourable prognosis respectively (P= 0.009 and P= 0.003). In the univariate analysis, PECAM-1(+)/ICAM-3(-) and HLA-DR(-)/ICAM-3(-) patients exhibited a significantly decreased overall survival compared to those with the exactly opposite gene expression patterns (P=0.0041 and P= 0.0091, respectively). Those patients who were HLA-DR(+ )/ICAM-3(+ )/PECAM-I(-) (n = 8) had a significantly higher survival rate compared to the rest of the group (n = 24) (P= 0.0289). CONCLUSION: PECAM-1, ICAM-3 and HLA-DR are representative markers of tumor expansion potential and host immune surveillance respectively. Their combined use may help us to identify high-risk patients who could benefit from more aggressive therapeutic protocols. 瞄准:与主要 non-Hodgkin 的胃的淋巴瘤在病人调查 PECAM-1, ICAM-3 和 HLA 医生抗原的预示的意义。方法:我们免疫组织化学地在 36 个 B 房间麦芽类型主要胃的淋巴瘤病人学习了 PECAM-1, ICAM-3 和 HLA 医生抗原表示。十非恶意并且十个健康胃的织物标本被用作控制。Clinicopathological 和幸存数据与染色的结果被相关。结果:HLA 医生抗原表示在 33 个胃的淋巴瘤病人(91.7%) 和 6 个非恶意的病人(54.5%) 被检测。PECAM-1 染色了 10 个病人(27.8%) 的肿瘤房间, 9 个病人(25%) 的 endothelial 并且煽动性有良性的胃的疾病的 4 个病人(40%) 渗入。ICAM-3 表示在 17 个病人(47.2%) 的肿瘤房间上被观察,当 5 个非恶意的病人(50%) 被染色时积极也。任何一个都没为任何学习的基因健康控制被染色。在里面多,变量分析, HLA 医生抗原和 PECAM-1 被证明是与联系的统计上重要的独立预示的因素一赞成并且不利预后分别地(P=0.009 和 P=0.003 ) 。在 univariate 分析, PECAM-1 (+)/ICAM-3 (-) 和 HLA 医生(-)/ICAM-3 (-) 病人与确切相反的基因表示模式与那些相比展出了显著地减少的全面幸存(P=0.0041 和 P=0.0091,分别地) 。是 HLA 医生(+)/ICAM-3 (+)/PECAM-1 (-)(n=8 ) 的那些病人让显著地更高的幸存与这个组(n=24 )(P=0.0289 ) 的其余部分相比评价。结论:PECAM-1, ICAM-3 和 HLA 医生分别地是肿瘤扩大潜力和主人免疫者监视的代表性的标记。他们的联合使用可以帮助我们识别能得益于更好攻击的治疗学的协议的高风险的病人。
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2006年第12期1924-1932,共9页 世界胃肠病学杂志(英文版)
基金 Supported by the Athens University and the Greek Ministry of Health and Welfare
关键词 PECAM-1 ICAM-3 HLA-DR Non-Hodgkin's gastric lymphoma PROGNOSIS 分子标记 PECAM-1 ICAM-3 HLA-DR 疾病预防 非霍奇金胃病 胃淋巴瘤
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  • 1[1]Frazee RC,Roberts J.Gastric lymphoma treatment.Medical versus surgical.Surg Clin North Am 1992; 72:423-431
  • 2[2]Azab MB,Henry-Amar M,Rougier P,Bognel C,Theodore C,Carde P,Lasser P,Cosset JM,Caillou B,Droz JP.Prognostic factors in primary gastrointestinal non-Hodgkin's lymphoma.A multivariate analysis,report of 106 cases,and review of the literature.Cancer 1989; 64:1208-1217
  • 3[3]Pozzi B,Hotz AM,Feltri M,Cornaggia M,Campiotti L,Bonato M,Pinotti G,Capella C.Primary gastric lymphomas.Clinicopathological study and evaluation of prognostic factors in 65 cases treated surgically Pathologica 2000; 92:503-515
  • 4[4]Charalambous GK,Gomatos IP,Konstadoulakis MM,Messaris EG,Manouras AJ,Apostolou AE,Leandros EA,Karayannis MK,Androulakis GA.Protein expression of bax,bcl-2,and p53 in patients with non-Hodgkin's gastric lymphoma:prognostic significance.World J Surg 2000; 24:608-614
  • 5[5]Benacerraf B.Role of MHC gene products in immune regulation.Science 1981; 212:1229-1238
  • 6[6]Kaufman JF,Auffray C,Korman AJ,Shackelford DA,Strominger J.The class Ⅱ molecules of the human and murine major histocompatibility complex.Cell 1984; 36:1-13
  • 7[7]Muller C,Ziegler A,Muller C,Hadam M,Waller HD,Wernet P,Muller G.Divergent expression of HLA-DC/MB,-DR,and -SB region products on normal and pathological tissues as detected by monoclonal antibodies.Immunobiology 1985; 169:228-249
  • 8[8]Ghosh AK,Moore M,Street AJ,Howat JM,Schofield PF.Expression of HLA-D sub-region products on human colorectal carcinoma.Int J Cancer 1986; 38:459-464
  • 9[9]Festenstein H.The biological consequences of altered MHC expression on tumours.Br Med Bull 1987; 43:217-227
  • 10[10]Holness CL,Bates PA,Little AJ,Buckley CD,McDowall A,Bossy D,Hogg N,Simmons DL.Analysis of the binding site on intercellular adhesion molecule 3 for the leukocyte integrin lymphocyte function-associated antigen 1.J Biol Chem 1995;270:877-884

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