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异常表达的 CD10 和 BCL6 在套细胞淋巴瘤中。

Aberrant expression of CD10 and BCL6 in mantle cell lymphoma.

机构信息

Surgical Pathology and Cytopathology Unit, Department of Medicine-DIMED, University of Padova, Padova, Italy.

Haematopathology Unit, Department of Hematology and Oncology/Department of Experimental Diagnostic and Specialty Medicine, Sant'Orsola University Hospital, Bologna, Italy.

出版信息

Histopathology. 2017 Nov;71(5):769-777. doi: 10.1111/his.13286. Epub 2017 Aug 8.

Abstract

AIMS

Mantle cell lymphoma (MCL) is characterized by distinctive histological and molecular features. Aberrant expression of BCL6 and CD10 has been reported occasionally, but the biological features of such cases are largely unknown. This study aimed to define the epidemiological, histological and cytogenetic characteristics of BCL6 and CD10-positive MCLs, also investigating possible biological features.

METHODS AND RESULTS

A total of 165 cases of cyclin D1 and t(11;14)(q13;q34)-positive MCLs were studied for CD10 and BCL6 immunohistochemical expression, which was documented in 26 of 165 (15.8%) cases (BCL6 17 of 165; CD10 11 of 165; BCL6 and CD10 co-expression two of 165). CD10-positivity was significantly more frequent in females (63.3%; P < 0.01). Either expression correlated significantly with higher mean proliferation index and higher prevalence of MUM1 positivity (P < 0.05). Fluorescence in-situ hybridization (FISH) for BCL6 (3q27) gene derangements was performed on the BCL6- and CD10-positive cases and 98 matched controls: amplifications were documented more frequently in BCL6-positive than -negative cases (50.0% versus 19.4% of cases) (P < 0.05). The mutational status of the variable immunoglobulin heavy chain genes (IGVH) was investigated by Sanger sequencing: five of the six successfully tested cases (83.3%) showed no somatic hypermutations.

CONCLUSIONS

Aberrant CD10 and BCL6 expression defines a subset of MCLs with higher mean Ki-67 index and higher prevalence of MUM1 expression. BCL6 protein positivity correlates with cytogenetic aberrations involving the BCL6 gene. Although examined successfully in few cases, the high prevalence of unmutated IGVH genes also points at a pregerminal cell origin for these phenotypically aberrant cases.

摘要

目的

套细胞淋巴瘤(MCL)的特征为独特的组织学和分子特征。偶尔会报道 BCL6 和 CD10 的异常表达,但此类病例的生物学特征在很大程度上尚不清楚。本研究旨在确定 BCL6 和 CD10 阳性 MCL 的流行病学、组织学和细胞遗传学特征,并研究可能的生物学特征。

方法和结果

共研究了 165 例 cyclin D1 和 t(11;14)(q13;q34)阳性的 MCL 病例,以检测 CD10 和 BCL6 的免疫组织化学表达,其中 26 例(15.8%)为阳性(BCL6 17/165;CD10 11/165;BCL6 和 CD10 共表达 2/165)。CD10 阳性在女性中更为常见(63.3%;P<0.01)。BCL6 和 CD10 的表达均与较高的平均增殖指数和较高的 MUM1 阳性率显著相关(P<0.05)。对 BCL6(3q27)基因重排的荧光原位杂交(FISH)在 BCL6 和 CD10 阳性病例及 98 例匹配对照中进行:在 BCL6 阳性病例中比阴性病例更常发现扩增(50.0%比病例的 19.4%)(P<0.05)。通过 Sanger 测序研究了可变免疫球蛋白重链基因(IGVH)的突变状态:在成功测试的 6 个病例中,有 5 个(83.3%)没有体细胞突变。

结论

异常的 CD10 和 BCL6 表达定义了 MCL 的一个亚组,其平均 Ki-67 指数较高,MUM1 表达率较高。BCL6 蛋白阳性与涉及 BCL6 基因的细胞遗传学异常相关。尽管在少数病例中成功检测到,但高未突变 IGVH 基因的患病率也表明这些表型异常病例起源于生发细胞。

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