Immunologic aspects of colorectal cancer progression

A. V. Tishina, L. Vladimirova, A. Sagakyants, E. Dzhenkova, I. A. Novikova, E. Zlatnik
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Abstract

Colorectal cancer remains in the leading positions in the structures of morbidity and mortality among both sexes. A large number of studies are aimed to reveal new biomarkers targeted at both early diagnosis and improving the effectiveness of drug therapy. Colorectal carcinoma (CC) is heterogeneous in its morphological, molecular and immunological aspects and is a heterogeneous disease. The existing molecular genetic classifications and biomarkers capable of predicting the effectiveness of therapy aren’t optimal enough. New prognostic markers would make it possible to identify a subgroup of patients with a high risk of tumor recurrence, for whom enhanced monitoring and diagnostic monitoring should be established, as well as the selection of highly effective methods in the treatment of colorectal cancer. It has been established that some immune cells in the tumor microenvironment are able to stimulate the development of disease progression. Cytokines and chemokines in the tumor microenvironment stimulate the development of metastases, and their serum levels reflect the current inflammatory response in the tumor tissue. The identification and analysis of immune markers involved in the processes of metastasis and the mechanisms of progression remains an important task of modern medicine. The purpose of the study was to analyze modern ideas about the importance of the immunological microenvironment in the progression of colorectal cancer. The effect of molecular heterogeneity of the tumor on the development of metastases, as well as on resistance to ongoing antitumor therapy. The review reflects the immunological characteristics of CC, including in the context of molecular biological subtypes. It describes the involvement of cells of the immune system (lymphocytes, macrophages) and their products (cytokines, chemokines) in the progression of colorectal cancer, including in the processes of neoangiogenesis, as well as the relationship of the T- and B-cell composition of the tumor microenvironment on the course of the disease. The review also shows the immunogenomic stratification of CC, which can be used to predict the response to immunotherapy for colorectal cancer.
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结直肠癌进展的免疫学问题
结肠直肠癌在男女发病率和死亡率中仍居首位。大量研究旨在揭示新的生物标志物,以实现早期诊断和提高药物治疗的有效性。结直肠癌(CC)在形态学、分子学和免疫学方面具有异质性,是一种异质性疾病。现有的分子遗传学分类和能够预测治疗效果的生物标志物还不够理想。新的预后标志物可以确定肿瘤复发风险较高的患者亚群,对这些患者应加强监测和诊断,并选择高效的结直肠癌治疗方法。已经证实,肿瘤微环境中的一些免疫细胞能够刺激疾病的发展。肿瘤微环境中的细胞因子和趋化因子会刺激肿瘤转移,其血清水平反映了肿瘤组织当前的炎症反应。鉴定和分析参与转移过程和进展机制的免疫标记物仍是现代医学的一项重要任务。本研究的目的是分析关于免疫微环境在结直肠癌进展中的重要性的现代观点。肿瘤的分子异质性对转移发展的影响,以及对正在进行的抗肿瘤治疗的耐药性。综述反映了 CC 的免疫学特征,包括在分子生物学亚型的背景下。它描述了免疫系统细胞(淋巴细胞、巨噬细胞)及其产物(细胞因子、趋化因子)参与结直肠癌进展的情况,包括参与新血管生成的过程,以及肿瘤微环境中 T 细胞和 B 细胞组成与疾病进程的关系。综述还展示了 CC 的免疫基因组分层,可用于预测结直肠癌免疫疗法的反应。
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