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滤泡树突状细胞中表皮生长因子受体的表达:滤泡树突状细胞肉瘤和Castleman病的共同特征。

Epidermal growth factor receptor expression in follicular dendritic cells: a shared feature of follicular dendritic cell sarcoma and Castleman's disease.

作者信息

Sun Xiaoping, Chang Kong-Chao, Abruzzo Lynne V, Lai Raymond, Younes Anas, Jones Dan

机构信息

Department of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Hum Pathol. 2003 Sep;34(9):835-40. doi: 10.1016/s0046-8177(03)00356-3.

Abstract

The factors regulating the growth of follicular dendritic cell (FDC) sarcoma are currently unknown. Using cDNA microarray analysis, we found that the epidermal growth factor receptor (EGFR) is expressed in FDC sarcoma. We immunohistochemically examined the expression of EGFR in a larger series of FDC sarcomas and in nonneoplastic FDCs. This included 8 cases of FDC sarcoma, 12 cases of hyaline vascular Castleman's disease (CD), 5 cases of human herpesvirus 8 (HHV8)-positive plasma cell CD, 7 cases of HHV8-negative plasma cell CD, 13 cases of reactive lymph nodes, 3 cases of reactive tonsils, 10 cases of follicular lymphoma, 6 cases of nodular mantle cell lymphoma, and 6 cases of angioimmunoblastic T-cell lymphoma. EGFR was expressed in tumor cells in 7 of 8 cases (88%) of FDC sarcoma (strongly in 4 cases and moderately in 3 cases). The single EGFR-negative case had an anaplastic appearance and a more aggressive clinical behavior. EGFR was also expressed by FDC in all types of CD (strongly in 4 cases, moderately in 16 cases, and weakly in 4 cases). Immunostaining results were negative or only weakly positive for EGFR in FDC of reactive lymph nodes and tonsils, and in the FDC networks of follicular lymphoma, mantle cell lymphoma, and angioimmunoblastic lymphoma. The up-regulation of EGFR in FDC of CD was paralleled by an increase in EGFR expression in the surrounding perifollicular fibroblastic reticulum cells suggesting coordinate regulation. These findings identify a differentially expressed growth regulatory receptor common to both FDC sarcoma and CD, identifying a target for possible therapy in unresectable or refractory cases.

摘要

目前尚不清楚调节滤泡树突状细胞(FDC)肉瘤生长的因素。通过cDNA微阵列分析,我们发现表皮生长因子受体(EGFR)在FDC肉瘤中表达。我们采用免疫组织化学方法检测了大量FDC肉瘤及非肿瘤性FDC中EGFR的表达情况。这包括8例FDC肉瘤、12例透明血管型Castleman病(CD)、5例人疱疹病毒8(HHV8)阳性浆细胞型CD、7例HHV8阴性浆细胞型CD、13例反应性淋巴结、3例反应性扁桃体、10例滤泡性淋巴瘤、6例结节性套细胞淋巴瘤和6例血管免疫母细胞性T细胞淋巴瘤。在8例FDC肉瘤中的7例(88%)肿瘤细胞中检测到EGFR表达(4例为强阳性,3例为中度阳性)。唯一1例EGFR阴性的病例具有间变外观且临床行为更具侵袭性。在所有类型的CD中,FDC也表达EGFR(4例为强阳性,16例为中度阳性,4例为弱阳性)。在反应性淋巴结和扁桃体的FDC中,以及在滤泡性淋巴瘤、套细胞淋巴瘤和血管免疫母细胞性淋巴瘤的FDC网络中,免疫染色结果显示EGFR呈阴性或仅为弱阳性。CD的FDC中EGFR的上调与周围滤泡周成纤维细胞网状细胞中EGFR表达的增加相平行,提示存在协同调节。这些发现确定了一种在FDC肉瘤和CD中均差异表达的生长调节受体,为不可切除或难治性病例的潜在治疗提供了靶点。

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