人类结直肠癌组织中的 CXCL10 表达及其与血清中 CXCL10 水平的相关性

IF 2.6 4区 医学 Q2 GENETICS & HEREDITY Cancer Genomics & Proteomics Pub Date : 2024-01-01 DOI:10.21873/cgp.20429
Lianbo Li, Kosuke Kanemitsu, Koji Ohnishi, Rin Yamada, Hiromu Yano, Yukio Fujiwara, Yuji Miyamoto, Yoshiki Mikami, Taizo Hibi, Hideo Baba, Yoshihiro Komohara
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引用次数: 0

摘要

背景/目的:CXCL10是CXC趋化因子家族的一员,它通过促进CXCR3阳性免疫细胞的趋化作用在免疫反应中发挥着至关重要的作用。我们研究了CXCL10的表达,以揭示其在结直肠癌中的功能意义:我们对 CXCL10 的表达及其临床病理相关性进行了生物信息学分析。随后,我们研究了血清中 CXCL10 水平与其在癌症组织中表达的相关性:结果:对 TCGA 数据库的分析表明,CXCL10 在 CRC 组织中的高表达与长期生存率的提高相关,并与淋巴结浸润和转移成反比。基因本体论》和《京都基因和基因组百科全书》的研究结果进一步证实,CXCL10和共调基因表达的升高与免疫激活和调节的增强有关,而免疫激活和调节是通过抑制NOD样受体信号通路介导的。单细胞分析指出,髓系细胞和巨噬细胞是 CXCL10 的主要来源。免疫组化评估显示,一部分癌细胞和巨噬细胞的 CXCL10 表达呈阳性。CXCL10阳性细胞主要位于肿瘤的浸润前沿。耐人寻味的是,我们的研究结果表明,血清中 CXCL10 的水平与其在癌症组织中的表达呈反相关:结论:CXCL10 的表达可能在调解结直肠癌浸润前沿的炎症反应中发挥作用,并且观察到其表达与血清 CXCL10 水平成反比。阐明 CXCL10 在结直肠癌中的不同作用,尤其是癌症组织 CXCL10 与血清 CXCL10 的不同功能至关重要。
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CXCL10 Expression in Human Colorectal Cancer Tissue and its Correlation With Serum Levels of CXCL10.

Background/aim: CXCL10, a member of the CXC chemokine family, plays a crucial role in immune response by facilitating the chemotaxis of CXCR3-positive immune cells. We examined the expression of CXCL10 to unravel its functional significance in colorectal cancer.

Materials and methods: Bioinformatics analysis was performed to investigate CXCL10 expression and its clinicopathological relevance. Subsequently, we examined the correlation between the serum levels of CXCL10 and its expression within cancer tissues.

Results: Analysis of the TCGA database revealed that elevated CXCL10 expression in CRC tissues correlates with improved long-term survival and is inversely associated with lymph node infiltration and metastasis. Insights from Gene Ontology and Kyoto Encyclopedia of Genes and Genomes further established a connection between increased CXCL10 and co-regulated gene expression with enhanced immune activation and regulation, mediated by the inhibition of the NOD-like receptor signaling pathway. Single-cell analysis pinpointed myeloid cells and macrophages as the primary sources of CXCL10. Immunohistochemical assessments revealed that a subset of cancer cells and macrophages are positive for CXCL10 expression. CXCL10-positive cells are predominantly located at the invasive front of the tumor. Intriguingly, our findings reveal an inverse correlation between serum CXCL10 levels and its expression in cancer tissues.

Conclusion: The expression of CXCL10 may play a role in mediating the inflammatory responses at the invasive front in colorectal cancer and is observed to be inversely correlated with serum CXCL10 levels. It is pivotal to elucidate the distinct roles of CXCL10 in colorectal cancer, particularly different functions of cancer-tissue CXCL10 from serum CXCL10.

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来源期刊
Cancer Genomics & Proteomics
Cancer Genomics & Proteomics ONCOLOGY-GENETICS & HEREDITY
CiteScore
5.00
自引率
8.00%
发文量
51
期刊介绍: Cancer Genomics & Proteomics (CGP) is an international peer-reviewed journal designed to publish rapidly high quality articles and reviews on the application of genomic and proteomic technology to basic, experimental and clinical cancer research. In this site you may find information concerning the editorial board, editorial policy, issue contents, subscriptions, submission of manuscripts and advertising. The first issue of CGP circulated in January 2004. Cancer Genomics & Proteomics is a journal of the International Institute of Anticancer Research. From January 2013 CGP is converted to an online-only open access journal. Cancer Genomics & Proteomics supports (a) the aims and the research projects of the INTERNATIONAL INSTITUTE OF ANTICANCER RESEARCH and (b) the organization of the INTERNATIONAL CONFERENCES OF ANTICANCER RESEARCH.
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