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C-MYC aberrations as prognostic factors in diffuse large B-cell lymphoma: a meta-analysis of epidemiological studies.C-MYC 异常作为弥漫性大 B 细胞淋巴瘤的预后因素:一项流行病学研究的荟萃分析。
PLoS One. 2014 Apr 16;9(4):e95020. doi: 10.1371/journal.pone.0095020. eCollection 2014.
2
Rearrangements of MYC gene facilitate risk stratification in diffuse large B-cell lymphoma patients treated with rituximab-CHOP.MYC 基因重排有助于利妥昔单抗-CHOP 治疗的弥漫性大 B 细胞淋巴瘤患者的风险分层。
Mod Pathol. 2014 Jul;27(7):958-71. doi: 10.1038/modpathol.2013.214. Epub 2013 Dec 13.
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[Significance and application of c-myc in diffuse large B-cell lymphoma].c-myc在弥漫性大B细胞淋巴瘤中的意义及应用
Zhonghua Bing Li Xue Za Zhi. 2013 Sep;42(9):638-40.
4
Prognostic significance of miR-34a and its target proteins of FOXP1, p53, and BCL2 in gastric MALT lymphoma and DLBCL.miR-34a 及其靶蛋白 FOXP1、p53、BCL2 在胃 MALT 淋巴瘤和 DLBCL 中的预后意义。
Gastric Cancer. 2014;17(3):431-41. doi: 10.1007/s10120-013-0313-3. Epub 2013 Nov 14.
5
MicroRNA profiling in ocular adnexal lymphoma: a role for MYC and NFKB1 mediated dysregulation of microRNA expression in aggressive disease.眼附属器淋巴瘤中的 microRNA 谱分析:在侵袭性疾病中,MYC 和 NFKB1 介导的 microRNA 表达失调的作用。
Invest Ophthalmol Vis Sci. 2013 Aug 5;54(8):5169-75. doi: 10.1167/iovs.13-12272.
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MYC protein expression and genetic alterations have prognostic impact in patients with diffuse large B-cell lymphoma treated with immunochemotherapy.在接受免疫化疗的弥漫性大 B 细胞淋巴瘤患者中,MYC 蛋白表达和基因改变具有预后影响。
Haematologica. 2013 Oct;98(10):1554-62. doi: 10.3324/haematol.2013.086173. Epub 2013 May 28.
7
Double-hit and triple-hit lymphomas arising from follicular lymphoma following acquisition of MYC: report of two cases and literature review.滤泡性淋巴瘤获得MYC后发生的双打击和三打击淋巴瘤:两例报告及文献复习
Int J Clin Exp Pathol. 2013;6(4):788-94. Epub 2013 Mar 15.
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Primary central nervous system diffuse large B cell lymphoma transformed from orbital mucosa-associated lymphoid tissue lymphoma: complete response to combined intrathecal and systemic rituximab.由眼眶黏膜相关淋巴组织淋巴瘤转化而来的原发性中枢神经系统弥漫性大B细胞淋巴瘤:鞘内注射与全身应用利妥昔单抗联合治疗后完全缓解
Ann Hematol. 2013 Jul;92(7):989-92. doi: 10.1007/s00277-012-1651-7. Epub 2012 Dec 16.
9
Expression of Myc, but not pSTAT3, is an adverse prognostic factor for diffuse large B-cell lymphoma treated with epratuzumab/R-CHOP.Myc 的表达,而非 pSTAT3,是接受依鲁替尼/利妥昔单抗+CHOP 方案治疗的弥漫性大 B 细胞淋巴瘤的不良预后因素。
Blood. 2012 Nov 22;120(22):4400-6. doi: 10.1182/blood-2012-05-428466. Epub 2012 Sep 27.
10
Chemokine receptors in gastric MALT lymphoma: loss of CXCR4 and upregulation of CXCR7 is associated with progression to diffuse large B-cell lymphoma.胃黏膜相关淋巴组织淋巴瘤中的趋化因子受体:CXCR4 的丢失和 CXCR7 的上调与向弥漫性大 B 细胞淋巴瘤的进展相关。
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C-MYC过表达预示黏膜相关淋巴组织淋巴瘤会发生侵袭性转化且预后不良。

C-MYC overexpression predicts aggressive transformation and a poor outcome in mucosa-associated lymphoid tissue lymphomas.

作者信息

Huang Wenting, Guo Lei, Liu Hongyan, Zheng Bo, Ying Jianming, Lv Ning

机构信息

Department of Pathology, Cancer Institute & Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences Beijing 100021, China.

Department of Pathology, China-Japan Friendship Hospital Beijing 100029, China.

出版信息

Int J Clin Exp Pathol. 2014 Aug 15;7(9):5634-44. eCollection 2014.

PMID:25337204
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4203175/
Abstract

Mucosa-associated lymphoid tissue (MALT) lymphoma is a relatively common, indolent B-cell lymphoma. MALT lymphoma with large tumor cells (LTCs) is believed to have the potential to transform to aggressive diffuse large B-cell lymphoma (DLBCL) which may have a poor prognosis. C-MYC is a transcription factor. Its translocation and overexpression predicts an inferior prognosis and poor response to therapy in cases of DLBCL. In the current study, C-MYC expression was detected in MALT lymphomas, and its relationship to the occurrence of LTCs, clinicopathological parameters and prognosis was assessed. A total of 69 cases were enrolled in the study, including 42 cases of MALT lymphoma without LTCs, 20 cases of MALT lymphoma with LTCs and 7 cases of DLBCL with a MALT lymphoma component (DLBCL+MALT). Immunohistochemistry and fluorescent in situ hybridization analyses were performed. In total, 15/42 (35.7%) cases were nuclear positive for C-MYC expression in the group without LTCs, whereas 15/20 (75.0%) and 4/7 (57.1%) cases were positive in the group with LTCs and in the group with DLBCL+MALT, respectively (P=0.004). Univariate and multivariate analysis were used to determine the correlations of C-MYC expression and clinicopathological parameters with overall survival (OS). C-MYC expression, Ann Arbor stage, LDH level and IPI were considerably associated with OS according to the univariate analysis. However, only C-MYC expression ≥ 20% showed a statistical significance in the multivariate analysis (HR=20.604, 95% CI: 1.909-222.412, P=0.013). Therefore, C-MYC overexpression may play an important role in aggressive transformation and is an independent prognostic factor in MALT lymphoma.

摘要

黏膜相关淋巴组织(MALT)淋巴瘤是一种相对常见的惰性B细胞淋巴瘤。伴有大肿瘤细胞(LTCs)的MALT淋巴瘤被认为有可能转化为侵袭性弥漫大B细胞淋巴瘤(DLBCL),其预后可能较差。C-MYC是一种转录因子。其易位和过表达预示着DLBCL患者预后较差且对治疗反应不佳。在本研究中,检测了MALT淋巴瘤中C-MYC的表达,并评估了其与LTCs发生、临床病理参数及预后的关系。本研究共纳入69例病例,包括42例无LTCs的MALT淋巴瘤、20例有LTCs的MALT淋巴瘤和7例伴有MALT淋巴瘤成分的DLBCL(DLBCL+MALT)。进行了免疫组织化学和荧光原位杂交分析。在无LTCs组中,共有15/42(35.7%)例C-MYC表达核阳性,而在有LTCs组和DLBCL+MALT组中,分别有15/20(75.0%)例和4/7(57.1%)例阳性(P=0.004)。采用单因素和多因素分析来确定C-MYC表达及临床病理参数与总生存期(OS)的相关性。单因素分析显示,C-MYC表达、Ann Arbor分期、乳酸脱氢酶(LDH)水平和国际预后指数(IPI)与OS显著相关。然而,多因素分析中仅C-MYC表达≥20%具有统计学意义(HR=20.604,95%CI:1.909-222.412,P=0.013)。因此,C-MYC过表达可能在侵袭性转化中起重要作用,并且是MALT淋巴瘤的独立预后因素。