Unraveling tumor cell‑tumor microenvironment crosstalk through antibody array technologies (Review).

IF 4.9 3区 医学 Q1 ONCOLOGY
International journal of oncology Pub Date : 2025-10-01 Epub Date: 2025-08-24 DOI:10.3892/ijo.2025.5787
Yanlin Wang, Shuhong Luo, Hua Dong, Ruo-Pan Huang
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引用次数: 0

Abstract

The tumor microenvironment (TME) consists of tumor cells, stromal cells, infiltrating immune cells and non‑cellular components such as extracellular matrix, blood vessels and a wide variety of secreted proteins. Evidence shows that beyond supporting tumor growth, the TME also promotes tumor cell proliferation and invasion and contributes to treatment resistance, ultimately affecting patient prognosis. Cell‑to‑cell communication within the TME is driven by secreted proteins such as cytokines, chemokines, growth factors and interferons, which are produced not only by tumor cells but also by various stromal cells and immune cells. These proteins form a complex signaling network that promotes tumor cell proliferation and invasion and enables tumors to evade innate and adaptive immune responses. Antibody arrays are a technology that can simultaneously screen hundreds of secreted proteins in complex biological samples, aiding in the exploration of this complex signaling network. By combining high‑throughput multiplex immunoassays such as antibody arrays with cellular and molecular biology techniques, researchers have uncovered complex regulatory mechanisms of cytokine networks within the TME. The present review summarized recent findings on the communication between tumor cells and the TME, as well as key secreted proteins essential for tumor progression and the development of therapeutic resistance. In addition, it discusses how high‑throughput antibody arrays contribute to our understanding of regulatory networks of secreted proteins in the TME.

Abstract Image

Abstract Image

通过抗体阵列技术揭示肿瘤细胞-肿瘤微环境串扰(综述)。
肿瘤微环境(TME)由肿瘤细胞、基质细胞、浸润性免疫细胞和非细胞成分如细胞外基质、血管和多种分泌蛋白组成。有证据表明,除了支持肿瘤生长外,TME还促进肿瘤细胞的增殖和侵袭,导致治疗抵抗,最终影响患者预后。TME内的细胞间通讯是由分泌的蛋白质驱动的,如细胞因子、趋化因子、生长因子和干扰素,这些蛋白质不仅由肿瘤细胞产生,也由各种基质细胞和免疫细胞产生。这些蛋白形成一个复杂的信号网络,促进肿瘤细胞增殖和侵袭,使肿瘤逃避先天和适应性免疫反应。抗体阵列是一种可以同时筛选复杂生物样品中数百种分泌蛋白的技术,有助于探索这种复杂的信号网络。通过将高通量多重免疫分析(如抗体阵列)与细胞和分子生物学技术相结合,研究人员发现了TME中细胞因子网络的复杂调控机制。本文综述了肿瘤细胞与TME之间的通讯,以及肿瘤进展和治疗耐药发展所必需的关键分泌蛋白的最新发现。此外,它还讨论了高通量抗体阵列如何有助于我们了解TME中分泌蛋白的调节网络。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.60
自引率
0.00%
发文量
157
审稿时长
2.1 months
期刊介绍: The main aim of Spandidos Publications is to facilitate scientific communication in a clear, concise and objective manner, while striving to provide prompt publication of original works of high quality. The journals largely concentrate on molecular and experimental medicine, oncology, clinical and experimental cancer treatment and biomedical research. All journals published by Spandidos Publications Ltd. maintain the highest standards of quality, and the members of their Editorial Boards are world-renowned scientists.
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