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Correlation between immune signature and high‐density lipoprotein cholesterol level in stage II/III colorectal cancer

机译:II / III期大肠癌免疫特征与高密度脂蛋白胆固醇水平的相关性

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摘要

An increasing amount of evidence suggests that high‐density lipoprotein cholesterol (HDL‐C) is related to a positive prognosis in various cancers. However, the correlation between HDL‐C and the immune signature and the prognostic role of HDL‐C in stage II/III colorectal cancer (CRC) has not been previously reported. A total of 667 CRC patients were enrolled and divided into two groups based on the lower limit of normal HDL‐C values (0.78 mmol/L). We used Kaplan‐Meier curves and the Cox regression model to analyze the prognostic role of HDL in both disease‐free survival (DFS) and overall survival (OS). Fifty‐five pairs of tumor tissues were selected according to the variation in HDL‐C levels (high or low) and the matched characterizes (ages, T stage, and N stage). Using immunohistochemistry, tumor tissues were stained with antibodies against CD3, CD8, CD163, iNOS, Forkhead box P3 (FOXP3), and CD33. We calculated the density of positively‐stained infiltrating cells in the tumor center (TC) and invasive margin (IM). We then used Spearman rank correlation to further investigate the relationship between HDL‐C levels and the immune signatures. Our results revealed that compared to patients with high HDL‐C levels, patients with low HDL‐C levels had poor 3‐year DFS (68.9% vs 83.1%, P = 0.032) and 5‐year OS rates (66.6% vs 85.3%, P = 0.002). We also identified a positive correlation between HDL‐C and CD3+, CD8+ and iNOS+ cells and a negative correlation between HDL‐C and CD163+ cells in both the TC and IM. This study reveals that a low HDL‐C level in stage II/III CRC patients predicts poor prognosis. The correlation between the HDL‐C level and immune signature in tissue specimens suggested that HDL‐C is likely to play an inhibitory role in tumor development via affecting immune responses.
机译:越来越多的证据表明,高密度脂蛋白胆固醇(HDL-C)与各种癌症的阳性预后有关。但是,HDL-C与免疫标记之间的相关性以及HDL-C在II / III期大肠癌(CRC)中的预后作用尚未见报道。共有667名CRC患者入组,根据​​正常HDL-C值的下限(0.78 mmol / L)分为两组。我们使用Kaplan-Meier曲线和Cox回归模型分析了HDL在无病生存期(DFS)和总体生存期(OS)中的预后作用。根据HDL-C水平的变化(高或低)和特征(年龄,T期和N期)来选择55对肿瘤组织。使用免疫组织化学,将肿瘤组织用针对CD3,CD8,CD163,iNOS,叉头盒P3(FOXP3)和CD33的抗体染色。我们计算了肿瘤中心(TC)和浸润边缘(IM)中染色阳性的浸润细胞的密度。然后,我们使用Spearman等级相关性进一步研究HDL-C水平与免疫特征之间的关系。我们的结果显示,与HDL‐C水平高的患者相比,HDL‐C水平低的患者3年DFS较差(68.9%对83.1%,P = 0.032)和5年OS率(66.6%对85.3% ,P = 0.002)。我们还发现HDL‐C与CD3 + ,CD8 + 和iNOS + 细胞之间呈正相关,而HDL‐C与CD3 + 和iNOS + 细胞之间呈负相关。 TC和IM中都有CD163 + 细胞。这项研究表明,II / III期CRC患者的HDL-C水平低预示了不良预后。 HDL-C水平与组织标本中的免疫特征之间的相关性表明,HDL-C可能通过影响免疫反应而在肿瘤发展中发挥抑制作用。

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