I期肺癌肿瘤微环境中细胞因子和细胞表面标志物的研究进展

Ogheneyoma Akpoviroro
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摘要

:将细胞表面标志物和细胞因子在早期癌症(LC)肿瘤微环境中的知识应用于临床实践的可能性,仍然是肿瘤学的一个发展方面,但可能是一个非常丰富的方面,而不是完全探索的方面。尽管通过LC筛查对LC的早期诊断在降低LC死亡率方面发挥了重要作用,但癌症复发也是一个同样重要的临床问题。LC肿瘤微环境中的细胞表面标志物和细胞因子可用于临床预后目的。这特别涉及风险分层和随后根据复发风险确定可能从术后早期辅助治疗中获益最多的患者。这些分子也有可能成为治疗靶点。然而,各种细胞因子和细胞表面标记物在LC和其他癌症的免疫微环境(IME)中的作用和作用,以及这些分子与浸润免疫细胞之间的相互作用,尚未得到充分阐述,在这方面仍有工作要做。本文试图讨论这些细胞表面标志物和细胞因子中的一些,它们可能在未来以分层评分和模型的形式作为早期LC的预测因子。这使用来自机构的I-III期患者的数据和从TCGA中提取的类似数据进行了2次单独的分析(n=233)。HLA-II用于IHC,通过基因分析确定淋巴细胞浸润。
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Narrative review of cytokines and cell surface markers in the tumor microenvironment of stage I lung cancer
: The possibility to apply the knowledge of cell surface markers and cytokines in the tumor microenvironment of early lung cancer (LC) in clinical practice, is still a developing facet of oncological medicine, but may possibly be a very fertile, not wholly explored facet. Although early diagnosis of LC through the efforts of LC screening has served an important role in decreasing LC mortality, cancer recurrence is also an equally important clinical concern. Cell surface markers and cytokines in the tumor microenvironment of LC may serve a clinical prognostic purpose. This is specifically with regard to risk stratification and subsequent identification of patients that may most benefit from early postoperative adjuvant therapy, based on their risk of recurrence. These molecules could also potentially serve as therapeutic targets. However, the roles and effects of various cytokines and cell surface markers in the immune microenvironment (IME) of LC and other cancers, as well as the interplay between these molecules and infiltrating immune cells, have not been fully elaborated, and there remains work to be done in this respect. This article attempts to discuss some of these cell surface markers and cytokines that may, in the future, serve as prognosticators for the early LC, possibly in the forms of stratification scores and models. This carried out 2 separate analyses using data from stage I-III patients from institution and similar data extracted from TCGA (n=233). HLA-II was for using IHC, lymphocyte infiltration was determined by genetic analysis.
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