CD30和CD56在淋巴母细胞淋巴瘤中的表达和临床意义:通过免疫组化对石蜡包埋组织的回顾性分析。

IF 0.7 4区 医学 Q4 PATHOLOGY
Fetal and Pediatric Pathology Pub Date : 2024-03-01 Epub Date: 2024-01-11 DOI:10.1080/15513815.2023.2301459
Shuqi Li, Shuang Zheng, Xinyi Huang, Wenhui Zhang, Fang Liu, Qinghua Cao
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引用次数: 0

摘要

背景:我们评估了淋巴母细胞淋巴瘤(LBL)中 CD30 和 CD56 的表达,并将评估结果与临床病理特征和预后相关联。研究方法:采用免疫组织化学(IHC)染色法,对 80 例淋巴母细胞淋巴瘤患者进行检测:使用两种 CD30 克隆抗体和一种 CD56 克隆抗体对 85 例福尔马林固定石蜡包埋的 LBL 标本进行免疫组化(IHC)染色。结果显示CD30在4.7%(克隆Ber-H2)或14.1%(克隆EPR4102)的LBL中弱表达和弥漫表达,而CD56在24.7%的LBL中表达。CD30 和 CD56 的表达与乳酸脱氢酶水平相关。CD56 阳性表达与预后不良密切相关。虽然 CD30 的表达显示出总生存率较低的趋势,但并未达到统计学意义。结论CD56 是一种潜在的阴性预后标志物。这些研究结果表明,CD30和CD56靶向疗法可能是LBL患者的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression and Clinical Significance of CD30 and CD56 in Lymphoblastic Lymphoma: A Retrospective Analysis on Paraffin-Embedded Tissues by Immunohistochemistry.

Background: We evaluated CD30 and CD56 expression in lymphoblastic lymphoma (LBL) and correlated the results with clinicopathological features and prognosis. Methods: Immunohistochemical (IHC) staining was performed on 85 formalin-fixed paraffin-embedded LBL specimens using two CD30 clones and one CD56 antibody clone. Results: Weak and diffuse expression of CD30 was expressed in 4.7% (clone Ber-H2) or 14.1% (clone EPR4102) in LBL, while CD56 was expressed in 24.7%. CD30 and CD56 expression correlated with lactate dehydrogenase levels. CD56-positive expression was closely associated with an unfavorable prognosis. Although CD30 expression exhibited a trend toward poorer overall survival, it did not reach statistical significance. Conclusion: CD56 is a potential negative prognostic marker. These findings suggest that CD30 and CD56 targeted therapies could be potential therapeutic targets for LBL patients.

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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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