前炎症介质和癌症相关趋化因子 CXCL8 作为肿瘤侵袭性、血管生成和疾病进展的预后指标,重点关注治疗意义和复发监测

Oral Oncology Reports Pub Date : 2025-03-01 Epub Date: 2025-02-05 DOI:10.1016/j.oor.2025.100723
Hema Shree K , Gayathri R , Vishnu Priya Veeraraghavan , Selvaraj J , Pratibha Ramani
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引用次数: 0

摘要

背景:口腔鳞状细胞癌(OSCC)是一种常见的恶性肿瘤,其特点是高发病率和死亡率。肿瘤微环境中的慢性炎症在OSCC的进展中起着关键作用,CXCL8或白细胞介素-8 (IL-8)作为一种重要的细胞因子参与了各种致瘤过程。IL-8促进血管生成、免疫逃逸和癌细胞干细胞,促进肿瘤侵袭和抵抗治疗。了解IL-8表达的纵向变化有助于了解OSCC的进展和治疗反应,可能指导个性化的治疗策略。目的探讨鳞状细胞癌患者IL-8表达的纵向变化趋势。评估IL-8水平与疾病进展、治疗结果和患者生存之间的相关性。评价IL-8作为生物标志物的预后价值及其作为治疗靶点的潜力。方法前瞻性纵向研究纳入75例OSCC患者,分为治疗前组、治疗后组和随访组。采集唾液样本,采用RT-PCR和ELISA检测IL-8的表达水平。使用混合效应模型和Kaplan-Meier生存分析分析IL-8表达的时间趋势及其与临床结果的关系。结果与对照组相比,OSCC患者IL-8水平显著升高。治疗后IL-8水平下降,但与对照组相比仍升高,较高水平与肿瘤晚期和较差分化相关。Kaplan-Meier分析显示,持续高IL-8表达的患者生存率降低。结论纵向监测IL-8的表达对OSCC的发病机制和治疗效果有重要意义。IL-8作为预后生物标志物和治疗靶点的作用值得进一步探索,以加强疾病管理和患者预后。
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Pro-inflammatory mediator and cancer-associated chemokine CXCL8 as a prognostic indicator of tumor aggressiveness, angiogenesis, and disease progression with focus on therapeutic implications and recurrence monitoring

Background

Oral Squamous Cell Carcinoma (OSCC) is a prevalent malignancy characterized by high morbidity and mortality. Chronic inflammation within the tumor microenvironment plays a pivotal role in OSCC progression, with CXCL8 or interleukin-8 (IL-8) emerging as a significant cytokine implicated in various pro-tumorigenic processes. IL-8 promotes angiogenesis, immune evasion, and cancer cell stemness, contributing to tumor aggression and resistance to therapy. Understanding longitudinal changes in IL-8 expression provides insights into OSCC progression and treatment responses, potentially guiding personalized therapeutic strategies.

Objectives

To investigate longitudinal trends in IL-8 expression among OSCC patients. To assess correlations between IL-8 levels and disease progression, treatment outcomes, and patient survival. To evaluate IL-8's prognostic value as a biomarker and its potential as a therapeutic target.

Methods

A prospective longitudinal study enrolled 75 OSCC patients divided into pre-treatment, post-treatment, and follow-up groups. Saliva samples were collected, and IL-8 expression levels were quantified using RT-PCR and ELISA. Temporal trends in IL-8 expression and associations with clinical outcomes were analyzed using mixed-effects models and Kaplan-Meier survival analysis.

Results

Significant elevation of IL-8 levels was observed in OSCC patients compared to controls. IL-8 levels decreased post-treatment but remained elevated compared to controls, with higher levels correlating with advanced tumor stages and poorer differentiation. Kaplan-Meier analysis demonstrated reduced survival probabilities in patients with persistently high IL-8 expression.

Conclusions

Longitudinal monitoring of IL-8 expression offers valuable insights into OSCC pathogenesis and treatment response. IL-8's role as a prognostic biomarker and therapeutic target warrants further exploration to enhance disease management and patient outcomes.
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