期刊文献+

原发性胃肠淋巴瘤p53基因与13q14染色体缺失与预后的关系 被引量:3

Association of absence of p53 gene and chromosome 13q14 variation with prognosis of primary gastrointestinal lymphoma
原文传递
导出
摘要 目的探讨p53基因与13@4染色体缺失在原发性胃肠淋巴瘤(PGIL)预后判断、指导治疗中的作用。方法采用改良的荧光标记的原位杂交(FISH)技术检测72例PGII.及30例淋巴结反应性增生患者石蜡切片中p53基因及13q14染色体缺失情况,分析其与PGIL预后的关系。结果①I期~Ⅱ期患者中30.2%(16/53)有p53基因缺失,Ⅲ期~Ⅳ期患者中63.2%(12/19)有p53基因缺失(x2=6.397,p=0.011);②黏膜相关组织(MALT)淋巴瘤中28.6%(12/42)有p53基因缺失,非MAI,T淋巴瘤中53.3%(16/30)有p53基因缺失(x2=4.515,P=0.034);③MALT淋巴瘤中,无基因或单基因改变者平均生存期为(39.25±22.73)个月,2种基因改变的患者平均生存期为(9.11±5.95)个月;I期~Ⅱ期患者中,无基因或单基因改变者平均生存期为(40.33±23.18)个月,2种基因改变的患者平均生存期为(20.61±18.90)个月。④单纯13q14缺失与肿瘤发生部位、病理类型、临床分期以及平均生存期无关,但同时合并p53基因缺失则预后差。结论p53基因缺失在非MALT淋巴瘤组及Ⅲ期~Ⅳ期患者中发生率较高。p53缺失或p53基因缺失与13q14染色体同时存在缺失的PGIL病例恶性程度高,患者平均生存期短于无基因或单基因改变者。 Objective To assess the role of p53 gene and absence of chromosome 13q14 in prognosis of primary gastrointestinal lymphoma(PGIL). Methods The expressions of p53 gene and chromosome 13q14 in paraffin sections from 72 patients with PGIL and 30 patients with lymph node reactive hyperplasia were detected by using improved FISH technique. The association of p53 gene and absence of chromosome 13q14 with PGIL prognosis was analyzed. Results (1) The p53 gene deletion in stage IⅠ-Ⅱ patients was accounted for 30.2% ,which was lower than that in stage Ⅲ-Ⅳ patients (63.2 %, X2 = 6. 397, P= 0.011). (2) There was significant difference between MALT lymphoma and non-MALT lymphomaas aspect to p53 gene deletion (28. 6% vs 53.3%, X2=4.515, P=0.034). (3) The average survival time was (39.25±22.73) and (40.33±23.18) months in MALT lymphoma and stage Ⅰ-Ⅱ patients with or without single gene variation respectively, and was (9. 11 ±5.95) and (20.61 ± 18.90) months in MALT lymphoma and stage []] ~ IV patients with two genes variation, respectively. (4) 13q14 deletion was not significantly related to location, pathological type and clinical staging of tumor as well as survival time. However, the prognosis was poor when both 13q14 and p53 deleted. Conclusions There is a high incidence of p53 gene deletion in non-MALT lymphoma and stage Ⅲ-Ⅳ patients. Those who have p53 gene and chromosome 13q14 abnormalities are of high degree of malignant,and the average survival time is shorter than patients with or without single gene deletion.
出处 《中华消化杂志》 CAS CSCD 北大核心 2010年第3期149-153,共5页 Chinese Journal of Digestion
关键词 原发性胃肠淋巴瘤 P53 预后 Primary gastrointestinal lymphoma p53 Prognosis
  • 相关文献

参考文献8

二级参考文献63

  • 1王焱,周晓军.胃肠道淋巴瘤的病理诊断[J].中华消化内镜杂志,2005,22(3):212-215. 被引量:4
  • 2俞谦,孙为豪,刘顺英,欧希龙,曹大中,俞婷,郭庆明,许曼华,沈云志.原发性胃肠道恶性淋巴瘤临床分析[J].中华消化内镜杂志,2005,22(1):34-36. 被引量:21
  • 3陈岗,何开玲,许良中.48例非霍奇金淋巴瘤中的p53基因突变[J].上海医科大学学报,1995,22(4):242-244. 被引量:3
  • 4Thieblemont C, Dumontet C, Bouafia F, et al, Outcome in relation to treatment modalities in 48 patients with localized gastric MALT lymphoma: a retrospective study of patients treated during 1976-2001[ J]. Leuk Lymphoma, 2003, 44 (2) : 257 -262.
  • 5Prskalo M, Sabaric B, Ticak M, et al. Helicobaeter pylorl and malignant disease of the stomach [ J ]. Lijec-Vjesn,2002, 124 (suppl 1) : 57-60.
  • 6Iwano M, Okazaki K, Uchida K, et al. Characteristics of gastric B- cell lymphoma of mucosa-associated lymphoid tissue type involving multiple organs [ J ] . J Gastroenterol, 2004, 39(8) :739-746.
  • 7Thieblemont C. Clinical presentation and management of marginal zone lymphomas [ J ]. Hematology Am Soc Hematol Educ Program, 2005(1) : 307-313.
  • 8Morgner A, Bayerdorffer E, Neubauer A, et al. Malignant tumors of the stomach. Gastric mucosa-associated lymphoid tissue lymphoma and Helicobacter pylori [ J ]. Gastroenterol Clin North Am, 2000, 29(3) : 593-607.
  • 9Psyrri A, Papageorgiou S, Economopoulos T. Primary extra nodal lymphomas of stomach : clinical presentation, diagnostic pitfalls and management [ J ]. Ann Oncol, 2008, 19 (12) : 1992-1999.
  • 10Richmond J, Bryant R, Trotman W, et al. FISH detection of t ( 14; 18 ) in follicular lymphoma on Papanicotaou-stained archival cytology slides [J]. Cancer, 2006, 108(3) : 198-204.

共引文献32

同被引文献18

  • 1周民,岑岭,薛永权.非霍奇金淋巴瘤的临床与骨髓细胞遗传学分析[J].中华医学遗传学杂志,2006,23(5):568-570. 被引量:6
  • 2Sabattini E, Bacci F, Sagramoso C, et al. WHO classification of tumours (ff haematopoietic and lymphoid tissues in 2008: an overview. Pathologica, 2010, 102: 83-7.
  • 3Kurian KM, Watson C J, Wyllie AH. DNA chip technology. J Pathol, 1999, 187: 267-271.
  • 4Offit K, Lo CF, Louie DC, et al. Rearrangement of the bcl-6 gene as a prognostic marker in diffuse large-cell lymphoma. N Engl J Med, 1994, 331: 74-80.
  • 5Barrans SL, O'Connor SJ, Evans PA, et al. Rearrangement of the bcl6 locus at 3q27 is an independent poor prognostic factor in nodal diffuse large B-cell lymphoma. Br J Haematol, 2002, 117: 322-332.
  • 6Winter JN, Weller EA, Homing SJ, et al. Prognostic significance of bcl-6 protein expression in DLBCL treated with CHOP or R-CHOP: a prospective correlative study. Blood, 2006, 107: 4207-4213.
  • 7Shustik J, Han G, Farinha P, et at. Correlations between bcl6 rearrangement and outcome in patients with diffuse large B-cell lymphoma tated with CHOP or R-CHOP. Haematologica, 2010, 95: 96-101.
  • 8Savage KJ, Johnson NA, Ben-Neriah S, et at. MYC gene rearrangements are associated with a poor prognosis in difflJse large B- cell lymphoma patients treated with R-CHOP chemotherapy. Blood, 2009, 114: 3533-3537.
  • 9Yoon SO, Jeon YK, Paik JH, et al. MYC translocation and an increased copy number predict poor prognosis in adult diffuse large B- cell lymphoma (DLBCL), especially in germinal centre-like B cell (GCB) type. Histopathol, 2008, 53:205-217.
  • 10Drakos E, Singh RR, Rassidakis GZ, et al. Activation of the p53 pathway by the MDM2 inhibitor nutlin-3a overcomes bcl2 overexpression in a preclinical model of diffuse large B-cell lymphoma associated with t(14; 18)(q32;q21). Leuk, 201 1, 25: 856-867.

引证文献3

二级引证文献18

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部