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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.

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。

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