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原发性肿瘤中 FOXP3+ 细胞密度对皮肤恶性黑色素瘤患者无预后影响。

FOXP3+ cell density in primary tumor has no prognostic impact in patients with cutaneous malignant melanoma.

机构信息

Center of Surgical and Molecular Tumor Pathology, National Institute of Oncology, 7-9 Ráth György u., Budapest, Hungary.

出版信息

Pathol Oncol Res. 2010 Sep;16(3):303-9. doi: 10.1007/s12253-010-9254-x. Epub 2010 Mar 21.

Abstract

Regulatory T cells (Tregs) have been implicated as inhibitors of antitumor immune reactions. However, data on the relevance of their prevalence at tumor sites in influencing disease outcome are controversial. The aim of our study was to investigate the role in tumor progression and the prognostic impact of the density of lymphocytes expressing FOXP3, a transcription factor expressed predominantly by CD4(+)CD25(+) Tregs, in primary cutaneous melanoma. We examined the infiltration of FOXP3(+) cells by immunohistochemistry in tumor samples from 97 patients and evaluated in relation to patient and tumor parameters. The degree of infiltration by FOXP3(+) cells did not show correlation with the thickness of melanomas. Moreover, no associations were found with metastasis formation during the 5-year follow-up period, patient survival, or any other clinicopathologic parameters studied. These results suggest that the presence of FOXP3(+) lymphocytes in primary tumors is not of prognostic importance in human cutaneous melanoma.

摘要

调节性 T 细胞(Tregs)被认为是抑制抗肿瘤免疫反应的细胞。然而,关于肿瘤部位 Tregs 丰度对疾病结局影响的相关数据仍存在争议。本研究旨在探讨在原发性皮肤黑素瘤中,表达叉头框蛋白 P3(FOXP3)的淋巴细胞密度在肿瘤进展中的作用及其对预后的影响。我们通过免疫组织化学法检测了 97 例患者肿瘤样本中 FOXP3+细胞的浸润情况,并结合患者和肿瘤参数进行了评估。FOXP3+细胞浸润程度与黑素瘤厚度无相关性。此外,在 5 年随访期间,FOXP3+细胞浸润程度与转移形成、患者生存或任何其他研究的临床病理参数均无关联。这些结果表明,FOXP3+淋巴细胞在原发性肿瘤中的存在对人类皮肤黑素瘤的预后并不重要。

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