Correlation of tumor-associated macrophage density and proportion of M2 subtypes with the pathological stage of colorectal cancer

Fouzia Fazal, Muhammad Arsalan Khan, Sumayyah Shawana, Rahma Rashid, Muhammed Mubarak
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Abstract

BACKGROUND Colorectal cancer (CRC) is a prevalent global malignancy with complex prognostic factors. Tumor-associated macrophages (TAMs) have shown paradoxical associations with CRC survival, particularly concerning the M2 subset. AIM We aimed to establish a simplified protocol for quantifying M2-like TAMs and explore their correlation with clinicopathological factors. METHODS A cross-sectional study included histopathological assessment of paraffin-embedded tissue blocks obtained from 43 CRC patients. Using CD68 and CD163 immunohistochemistry, we quantified TAMs in tumor stroma and front, focusing on M2 proportion. Demographic, histopathological, and clinical parameters were collected. RESULTS TAM density was significantly higher at the tumor front, with the M2 proportion three times greater in both zones. The tumor front had a higher M2 proportion, which correlated significantly with advanced tumor stage (P = 0.04), pathological nodal involvement (P = 0.04), and lymphovascular invasion (LVI, P = 0.01). However, no significant association was found between the M2 proportion in the tumor stroma and clinicopathological factors. CONCLUSION Our study introduces a simplified protocol for quantifying M2-like TAMs in CRC tissue samples. We demonstrated a significant correlation between an increased M2 proportion at the tumor front and advanced tumor stage, nodal involvement, and LVI. This suggests that M2-like TAMs might serve as potential indicators of disease progression in CRC, warranting further investigation and potential clinical application.
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肿瘤相关巨噬细胞密度和 M2 亚型比例与结直肠癌病理分期的相关性
背景 大肠癌(CRC)是一种全球流行的恶性肿瘤,其预后因素复杂。肿瘤相关巨噬细胞(TAMs)与 CRC 的存活率有着矛盾的关系,尤其是 M2 亚群。目的 我们旨在建立一个简化的方案来量化 M2 样 TAMs,并探讨它们与临床病理因素的相关性。方法 一项横断面研究包括对 43 例 CRC 患者的石蜡包埋组织块进行组织病理学评估。我们使用 CD68 和 CD163 免疫组化技术对肿瘤基质和前部的 TAMs 进行了量化,重点是 M2 的比例。我们还收集了人口统计学、组织病理学和临床参数。结果 肿瘤前沿的 TAM 密度明显更高,两个区域的 M2 比例均为前者的三倍。肿瘤前沿的 M2 比例较高,这与肿瘤晚期(P = 0.04)、病理结节受累(P = 0.04)和淋巴管侵犯(LVI,P = 0.01)显著相关。然而,在肿瘤基质中的 M2 比例与临床病理因素之间没有发现明显的关联。结论 我们的研究介绍了一种用于量化 CRC 组织样本中 M2 样 TAMs 的简化方案。我们发现肿瘤前沿的 M2 比例增加与肿瘤晚期、结节受累和 LVI 之间存在明显相关性。这表明 M2 样 TAMs 可作为 CRC 疾病进展的潜在指标,值得进一步研究和临床应用。
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