卵巢癌上皮间质微环境肿瘤相关免疫细胞受体表型特征

Q4 Medicine
V. N. Zhurman
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引用次数: 0

摘要

在所有组织学类型中,浆液性癌占85%。由于明显的异质性(在分子和遗传水平上)和化疗耐药,寻找肿瘤消除的活性靶点出现困难。的目标。建立微环境肿瘤相关免疫细胞群体组成与浆液性卵巢癌分期之间的联系。材料和方法。对74例浆液性卵巢癌的病理解剖资料进行了分析。采用单克隆抗体检测样品中的抗原:CD3、CD4、CD8、CD11b、CD14和CD16。结果。免疫组化研究结果表明,在微环境免疫细胞的组成中,在肿瘤过程的各个阶段(IIV)中,以巨噬细胞(CD11b+、CD14+)为代表的细胞数量最多,其次是CD3+淋巴细胞,其次是CD8+和CD4+, CD16+细胞数量最少。结论。免疫组化研究发现,微环境肿瘤相关免疫细胞的种群组成与浆液性卵巢癌的分期之间存在多向趋势。随着疾病分期的增加,无论肿瘤分化程度如何,巨噬细胞(CD11b+、CD14+)和淋巴细胞(CD3+、CD16+)数量均减少。随着肿瘤分期的增加,CD4+和CD8+群体数量减少,但在这种情况下,分化程度起着显著的作用,即肿瘤分期越高,分化程度越低,检测到的细胞越少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics of the receptor phenotype of tumor-associated immune cells of the epithelial-mesenchymal microenvironment of ovarian cancer
Among all histological types, serous carcinomas account for up to 85%. Due to pronounced heterogeneity (at the molecular and genetic level) and chemoresistance, difficulties arise in finding active targets for tumor elimination. Aim. To establish a link between the population composition of tumor-associated immune cells of the microenvironment and the stage of serous ovarian cancer. Materials and methods. The analysis of the pathologic and anatomical material in 74 patients with serous ovarian cancer was carried out. Monoclonal antibodies were used to determine antigens in the samples: CD3, CD4, CD8, CD11b, CD14 and CD16. Results. The obtained results of the immunohistochemical study showed that in the composition of the immune cells of the microenvironment, the largest number of cells, at all stages (IIV) of the oncological process, are represented by macrophages (CD11b+, CD14+), CD3+ lymphocytes are in second place in terms of the number of cells, followed by CD8+ and CD4+ and the smallest number of CD16+ cells. Conclusion. As a result of the immunohistochemical study, a multidirectional trend was found between the population composition of tumor-associated immune cells of the microenvironment and the stage of serous ovarian cancer. With an increase in the stage of the disease, the number of macrophages (CD11b+, CD14+) and lymphocytes (CD3+, CD16+) decreased regardless of the degree of differentiation of the tumor. With an increase in the tumor stage, the number of CD4+ and CD8+ populations decreased, but in this case, the degree of differentiation played a significant role, i.e. the higher the tumor stage and the lower the degree of differentiation, the fewer cells were detected.
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来源期刊
Journal of Modern Oncology
Journal of Modern Oncology Medicine-Oncology
CiteScore
0.50
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5 weeks
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