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CD24是人类乳腺癌的一个标志物。

CD24 is a marker for human breast carcinoma.

作者信息

Fogel M, Friederichs J, Zeller Y, Husar M, Smirnov A, Roitman L, Altevogt P, Sthoeger Z M

机构信息

Tumor Immunology Research Laboratory, Kaplan Hospital, Rehovot, Israel.

出版信息

Cancer Lett. 1999 Aug 23;143(1):87-94. doi: 10.1016/s0304-3835(99)00195-0.

DOI:10.1016/s0304-3835(99)00195-0
PMID:10465342
Abstract

CD24 is a small, mucin-type glycosylphosphatidylinositol-linked cell surface molecule expressed by neutrophils, pre B lymphocytes and certain human tumor cell lines. CD24 has been identified as a ligand for P-selectin in both mouse and human cells. We previously reported that the P-selectin-CD24 binding pathway is important for the binding of the breast carcinoma cell line KS to platelets and the rolling of these cells on endothelial P-selectin. In the present study we have analyzed the expression of CD24 on human breast carcinoma cell lines and on fresh breast carcinoma specimens using the CD24-specific antibody ML-5. Our study clearly demonstrates that CD24 is abundantly expressed on cell lines and fresh tissues of breast carcinomas. We find a differential expression of CD24 in breast carcinomas (cytoplasmic pattern) versus benign breast lesions (apical pattern). Moreover, the intensity of CD24 expression increases with the histological grade of the tumor. Thus, CD24 expression might be a useful marker for human breast carcinoma and play a role in facilitating metastasis by the interaction between tumor cells and platelets or endothelial cells.

摘要

CD24是一种小分子、粘蛋白型糖基磷脂酰肌醇连接的细胞表面分子,由中性粒细胞、前B淋巴细胞和某些人类肿瘤细胞系表达。在小鼠和人类细胞中,CD24已被确定为P-选择素的配体。我们之前报道过,P-选择素-CD24结合途径对于乳腺癌细胞系KS与血小板的结合以及这些细胞在内皮P-选择素上的滚动很重要。在本研究中,我们使用CD24特异性抗体ML-5分析了CD24在人乳腺癌细胞系和新鲜乳腺癌标本上的表达。我们的研究清楚地表明,CD24在乳腺癌的细胞系和新鲜组织中大量表达。我们发现CD24在乳腺癌(细胞质模式)与良性乳腺病变(顶端模式)中存在差异表达。此外,CD24表达强度随肿瘤组织学分级增加而增加。因此,CD24表达可能是人类乳腺癌的一个有用标志物,并通过肿瘤细胞与血小板或内皮细胞之间的相互作用在促进转移中发挥作用。

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1
CD24 is a marker for human breast carcinoma.CD24是人类乳腺癌的一个标志物。
Cancer Lett. 1999 Aug 23;143(1):87-94. doi: 10.1016/s0304-3835(99)00195-0.
2
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A comparison of the patterns of laminin expression in fibroadenoma, fibrocystic diseases, pre-invasive and invasive ductal breast carcinoma.纤维腺瘤、纤维囊性疾病、乳腺导管原位癌及浸润性导管癌中层粘连蛋白表达模式的比较。
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CD24, a mucin-type glycoprotein, is a ligand for P-selectin on human tumor cells.CD24是一种粘蛋白型糖蛋白,是人类肿瘤细胞上P选择素的配体。
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Immunohistochemical distinction of invasive from noninvasive breast lesions: a comparative study of p63 versus calponin and smooth muscle myosin heavy chain.免疫组织化学区分浸润性与非浸润性乳腺病变:p63与钙调蛋白及平滑肌肌球蛋白重链的比较研究
Am J Surg Pathol. 2003 Jan;27(1):82-90. doi: 10.1097/00000478-200301000-00009.
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CD24 mediates rolling of breast carcinoma cells on P-selectin.CD24介导乳腺癌细胞在P-选择素上滚动。
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Breast carcinoma in sclerosing adenosis: a clinicopathological and immunophenotypical analysis on 206 lesions.硬化性腺病中的乳腺浸润性癌:206 例病变的临床病理和免疫表型分析。
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CD24 expression in ductal carcinoma in situ and invasive ductal carcinoma of breast: an immunohistochemistry-based pilot study.乳腺导管原位癌和浸润性导管癌中CD24的表达:一项基于免疫组织化学的初步研究。
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Survivin in breast lesions: immunohistochemical analysis of 196 cases.乳腺病变中的生存素:196例免疫组织化学分析
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Cytokeratin intermediate filament expression in benign and malignant breast disease.细胞角蛋白中间丝在乳腺良恶性疾病中的表达
J Clin Pathol. 1995 Jan;48(1):26-32. doi: 10.1136/jcp.48.1.26.

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2
IMM47, a humanized monoclonal antibody that targets CD24, exhibits exceptional anti-tumor efficacy by blocking the CD24/Siglec-10 interaction and can be used as monotherapy or in combination with anti-PD1 antibodies for cancer immunotherapy.IMM47是一种靶向CD24的人源化单克隆抗体,通过阻断CD24/Siglec-10相互作用展现出卓越的抗肿瘤疗效,可作为单一疗法或与抗PD1抗体联合用于癌症免疫治疗。
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3
Identification of CD24 as a marker of Patched1 deleted medulloblastoma-initiating neural progenitor cells.
鉴定 CD24 作为缺失 Patched1 的髓母细胞瘤起始神经祖细胞的标志物。
PLoS One. 2019 Jan 18;14(1):e0210665. doi: 10.1371/journal.pone.0210665. eCollection 2019.
4
CD24 expression and stem-associated features define tumor cell heterogeneity and tumorigenic capacities in a model of carcinogenesis.CD24表达与干细胞相关特征在致癌模型中界定肿瘤细胞异质性和致瘤能力。
Cancer Manag Res. 2018 Nov 16;10:5767-5784. doi: 10.2147/CMAR.S176654. eCollection 2018.
5
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Oncotarget. 2017 Feb 7;8(6):10114-10135. doi: 10.18632/oncotarget.14357.
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Oncol Lett. 2016 Oct;12(4):2728-2733. doi: 10.3892/ol.2016.4987. Epub 2016 Aug 10.
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Virchows Arch. 2016 Sep;469(3):285-95. doi: 10.1007/s00428-016-1966-1. Epub 2016 Jun 10.
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Clin Med Insights Pathol. 2015 Jan 7;8:1-16. doi: 10.4137/CPath.S19615. eCollection 2015.
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