PU.1 is a nuclear factor of immunocompetent cells of tumor stroma in colorectal cancer

Q4 Medicine
O. Kovaleva, A. Gratchev, P. Podlesnaya, M. Rashidova, D. Samoilova, N. Sokolov, Z. Mamedli, D. Kudlay, N. Kushlinskii
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引用次数: 0

Abstract

Introduction. Tumor-associated macrophages (TAMs) are traditionally considered to be a pro-tumor fac-tor that promotes the growth of various tumors; however, for colorectal carcinomas (CRC), the prognostic significance of TAMs has not been fully determined, which may be due to the lack of macrophage markers suitable for this tumor type. The aim of this work was to study the expression of the nuclear marker of stromal cells PU.1 in colorectal tumors and its association with the clinical and morphological tumor characteristics. Materials and methods. We performed an immunohistochemical analysis to assess the expression of PU.1, CD68, and CD20 in 85 primary CRCs. The Mann-Whitney test was used to determine statistically significant differences in independent groups. Correlation analysis of the expression of the studied protein was carried out by determining the Spearman’s rank correlation coefficient. Differences were considered statistically significant at p <0.05. Results. We analyzed the expression of PU.1, CD68, and CD20 in CRC and detected positive PU.1 and CD68 expressions in tumor stromal cells in all of the studied samples. Expression of CD20 was observed in 87% of cases. We showed that in colorectal tumors all CD68+ or CD20+ cells express PU.1 and that PU.1 and CD20 were significantly associated with the disease stage (p=0.036 and p=0.002) and the presence or absence of regional metastases (p=0.022 and p=0.007). In addition, PU.1 showed a significant correlation with the distant metastases’ presence and tumor localization (p=0.031 and p=0.022). Higher content of PU.1 was typical for colon tumors without metastases. CD20 also showed a significant association with tumor size (p=0.025). No significant correlations with clinical and morphological features were found for CD68. We also demonstrated that the number of PU.1+ cells in tumors significantly positively correlates with CD68 (r=0.231, p=0.036) and CD20 (r=0.267, p=0.015). Conclusion. The results of this study indicate that PU.1 can be considered as an independent marker of a favorable prognosis in CRC patients. Keywords: colorectal cancer, expression, CD20, CD68, PU.1, macrophages, B-cells
PU.1是结直肠癌肿瘤间质免疫活性细胞的核因子
介绍。肿瘤相关巨噬细胞(Tumor-associated macrophages, tam)传统上被认为是促进多种肿瘤生长的促瘤因子;然而,对于结直肠癌(CRC), tam的预后意义尚未完全确定,这可能是由于缺乏适合这种肿瘤类型的巨噬细胞标志物。本研究旨在探讨基质细胞核标记物PU.1在结直肠肿瘤中的表达及其与肿瘤临床和形态特征的关系。材料和方法。我们进行了免疫组织化学分析,以评估PU.1、CD68和CD20在85例原发性crc中的表达。使用Mann-Whitney检验来确定独立组的统计学显著差异。通过测定Spearman 's秩相关系数对所研究蛋白的表达进行相关分析。p <0.05认为差异有统计学意义。结果。我们分析了PU.1、CD68和CD20在结直肠癌中的表达,并在所有研究样本的肿瘤基质细胞中检测到PU.1和CD68的阳性表达。87%的病例表达CD20。我们发现,在结直肠肿瘤中,所有CD68+或CD20+细胞都表达PU.1,并且PU.1和CD20与疾病分期(p=0.036和p=0.002)和是否存在区域转移(p=0.022和p=0.007)显著相关。此外,PU.1与远处转移灶的存在和肿瘤的定位有显著相关性(p=0.031和p=0.022)。未发生转移的结肠肿瘤具有较高的PU.1含量。CD20与肿瘤大小也有显著相关性(p=0.025)。CD68与临床和形态学特征无显著相关性。我们还发现肿瘤中PU.1+细胞的数量与CD68 (r=0.231, p=0.036)和CD20 (r=0.267, p=0.015)呈显著正相关。结论。本研究结果提示,PU.1可作为结直肠癌患者预后良好的独立标志物。关键词:结直肠癌,表达,CD20, CD68, PU.1,巨噬细胞,b细胞
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来源期刊
Clinical and Experimental Morphology
Clinical and Experimental Morphology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
0.60
自引率
0.00%
发文量
18
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