微环境在卵巢肿瘤营养中的作用

L. Khalikova, N. Shevlyuk, S. Gantsev, A. A. Khalikov, I. R. Khasanova
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引用次数: 0

摘要

背景。转移是恶性肿瘤的一个可怕的并发症,治疗并不总是有效的晚期恶性肿瘤。转移是一个多步骤的过程,包括癌细胞从原发肿瘤脱离、内渗、外渗和侵入靶器官。早期转移阶段已经被很好地理解,而肿瘤微环境对疾病进展和进展的影响仍然是一个有争议的问题。卵巢癌转移性大网膜适应性和反应性的免疫组织化学研究。材料和方法。我们检查了40例3a期和b期卵巢癌患者的大网膜组织样本。光镜下,样品用10%福尔马林固定,脱水,石蜡包埋,用梅耶氏血红素和伊红染色。免疫组化检测采用抗CD7、CD4、CD8、cd68、VEGF、D2-40和CD44蛋白的单克隆抗体。统计数据分析采用Statistica v. 7.0软件。结果和讨论。大网膜组织分析显示转移灶的白细胞库包封病例。在包封中观察到较高的CD7+和CD8+细胞计数,可能影响大网膜的反应性和适应性。在缺乏包封的大网膜样品中也检测到更高的cd44表达细胞计数。血管生成标志物表达细胞(如VEGF和CD34)在转移灶缺乏白细胞库包埋的大网膜组织中占主导地位。肿瘤微环境中的事件可能表明器官适应性保留或降低,后者促进疾病进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of Microenvironment in Ovarian Tumourisation
Background. Metastasis is a formidable complication of malignant neoplasms, with therapy not always effective in advanced malignancy. Metastasis is a multistep process involving the cancer cell detachment from primary tumour, intravasation, extravasation and invasion into the target organ. Early metastasis stages are well understood, whilst the impact of tumour microenvironment on the disease progression and advancement remains a matter of debate.Aim. An immunohistochemical study of the adaptive and reactive properties of greater omentum with metastatic involvement in ovarian cancer.Materials and methods. We examined greater omentum tissue samples from 40 patients with verifi ed stage 3a and b ovarian cancers. For light microscopy, samples were fi xed in 10 % formalin, dehydrated, paraffi n-embedded and stained with Mayer’s haematoxylin and eosin. Immunohistochemical assays used monoclonal antibodies against CD7, CD4, CD8, CD 68, VEGF, D2-40 and CD44 proteins. Statistical data analysis was performed with Statistica v. 7.0 soft ware.Results and discussion. Analyses of the greater omentum tissues revealed cases of leucocyte-bank encapsulation of metastatic foci. Higher CD7+ and CD8+ cell counts were observed in encapsulation, possibly influencing the greater omentum reactive and adaptive properties. Higher CD44-expressing cell counts were also detected in greater omentum samples lacking encapsulation. Angiogenesis marker-expressing cells (e.g., VEGF and CD34) predominated in greater omentum tissues lacking leucocyte-bank encapsulation of metastatic foci.Conclusion. Events in tumour microenvironment may be indicative of a preserved or reduced organ adaptivity, the latter facilitating disease progression.
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