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抗着丝粒蛋白CENP - F自身抗体患者中肿瘤形成的高频率。

High frequency of neoplasia in patients with autoantibodies to centromere protein CENP-F.

作者信息

Rattner J B, Rees J, Whitehead C M, Casiano C A, Tan E M, Humbel R L, Conrad K, Fritzler M J

机构信息

Department of Anatomy, University of Calgary, Alta.

出版信息

Clin Invest Med. 1997 Oct;20(5):308-19.

PMID:9336656
Abstract

OBJECTIVE

To study the clinical features of patients with autoantibodies to centromere protein CENP-F and the frequency of CENP-F autoantibodies in patients with various diseases.

DESIGN

Retrospective clinical and serologic study.

METHODS

Thirty-six patients with anti-CENP-F were identified by a characteristic pattern of indirect immunofluorescence (IIF) on HEp-2 cells. Fifty patients with melanoma, 50 with breast cancer, 10 with lung cancer, 354 with systemic sclerosis, 120 with systemic lupus erythematosus and 50 with rheumatoid arthritis were also studied. Recombinant proteins were produced from 5 CENP-F cDNA clones representing amino acids 2192-3317 (p-F1), 5561-7126 (p-F2), 5892-6883 (p-F3), 7538-10,116 (p-F4) and 9242-10,096 (p-F5). The presence of CENP-F antigen was studied in a breast carcinoma cell line, cryosections of breast carcinoma, normal breast tissue and tonsils.

RESULTS

Twenty-two of 36 patients with CENP-F antibodies had neoplasms; breast (9/22) and lung (5/22) cancer were the most common diagnoses. Thirty-three sera were available for further study; when tested for reactivity to the recombinant peptides, the sera of 21 of 21 patients with neoplasms and 5 of 12 patients with other diseases bound the C-terminal p-F4 peptide. When the terminal third of the p-F4 peptide (p-F5) was studied, a significant difference in pattern of reactivity was not detected. By comparison, the frequency of reactivity with peptides representing other domains of CENP-F was less than that with p-F4 (p-F2 > p-F3 > p-F1). CENP-F autoantibodies were not found in any of the control sera from patients with systemic lupus erythematosus, rheumatoid arthritis or systemic sclerosis or in unselected sera from various malignancies. CENP-F antigens were identified in breast carcinoma tissue but were rarely observed in normal tissues.

CONCLUSIONS

A high proportion of individuals with CENP-F antibodies have neoplasia, and there is a bias among their sera for reactivity with determinants in the carboxy terminal domain of CENP-F. CENP-F antigens appear to be highly expressed in malignant tissues.

摘要

目的

研究着丝粒蛋白CENP - F自身抗体患者的临床特征以及各种疾病患者中CENP - F自身抗体的频率。

设计

回顾性临床和血清学研究。

方法

通过HEp - 2细胞上间接免疫荧光(IIF)的特征模式鉴定出36例抗CENP - F患者。还研究了50例黑色素瘤患者、50例乳腺癌患者、10例肺癌患者、354例系统性硬化症患者、120例系统性红斑狼疮患者和50例类风湿关节炎患者。从5个CENP - F cDNA克隆中制备重组蛋白,这些克隆分别代表氨基酸2192 - 3317(p - F1)、5561 - 7126(p - F2)、5892 - 6883(p - F3)、7538 - 10116(p - F4)和9242 - 10096(p - F5)。在乳腺癌细胞系、乳腺癌冷冻切片、正常乳腺组织和扁桃体中研究CENP - F抗原的存在情况。

结果

36例CENP - F抗体患者中有22例患有肿瘤;乳腺癌(9/22)和肺癌(5/22)是最常见的诊断。有33份血清可用于进一步研究;当检测其对重组肽的反应性时,21例肿瘤患者中的21例血清以及12例其他疾病患者中的5例血清与C末端p - F4肽结合。当研究p - F4肽的末端三分之一(p - F5)时,未检测到反应模式的显著差异。相比之下,与代表CENP - F其他结构域的肽的反应频率低于与p - F4的反应频率(p - F2 > p - F3 > p - F1)。在系统性红斑狼疮、类风湿关节炎或系统性硬化症患者的任何对照血清中以及各种恶性肿瘤的未选择血清中均未发现CENP - F自身抗体。在乳腺癌组织中鉴定出CENP - F抗原,但在正常组织中很少观察到。

结论

高比例的CENP - F抗体个体患有肿瘤,并且他们的血清中与CENP - F羧基末端结构域中的决定簇反应存在偏差。CENP - F抗原似乎在恶性组织中高度表达。

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