肿瘤浸润 B 细胞抑制鼻咽癌转移
Tumor-infiltrating B cells inhibit nasopharyngeal carcinoma metastasis.
本研究表明,TIL-B在NPC的抗肿瘤免疫中发挥重要的调节作用,并提示其治疗潜力,为开发基于B细胞或靶向TLS的免疫治疗策略提供了依据。
英文原题:High Tumoral CD24 Expression and Low CD3(+) Tumor-Infiltrating Lymphocytes as a Biomarker for High-Risk Locally Advanced Nasopharyngeal Carcinoma.
High Tumoral CD24 Expression and Low CD3(+) Tumor-Infiltrating Lymphocytes as a Biomarker for High-Risk Locally Advanced Nasopharyngeal Carcinoma.
这些结果提示,将肿瘤CD24表达与CD3 + TIL密度联合作为LA-NPC的预后因素具有实用性,并可能应用于疾病管理和未来试验设计。
引言:TNM分期在局部晚期(LA)鼻咽癌(NPC),即III期或IV期NPC中的价值有限,这凸显了对预后标志物的需求。在此,我们旨在评估癌症干细胞标志物BMI1、ALDH1、CD44和CD24,以及上皮-间质转化标志物vimentin作为LA-NPC新型预后标志物的能力。 方法:使用了一个由83例LA-NPC患者组成的队列,该队列此前为另一项目标不同的试验所招募。采用免疫组织化学评估组织切片中的标志物表达,并使用Kaplan-Meier法和Cox回归分析分析表达与生存结局的关联。 结果:BMI1和ALDH1的表达与生存无关。CD24、CD44和vimentin的肿瘤表达与无病生存期(DFS)显著相关,而仅CD24的表达也与总生存期(OS)显著相关。事实上,CD24表达成为一个独立预后因素,因为它在单因素和多因素Cox回归分析中均与生存相关。有趣的是,将肿瘤细胞中CD24表达状态与CD3+TIL(肿瘤浸润淋巴细胞)密度这一微环境/免疫相关标志物相结合,识别出一个具有最差DFS和OS的高危亚组。 结论:这些结果提示,将肿瘤CD24表达与CD3+TIL密度相结合作为LA-NPC的预后因素具有实用性,并可能在疾病管理和未来试验设计中得到应用。我们的发现还凸显了将免疫相关因素和癌症干细胞相关因素相结合用于癌症个体化治疗策略的潜力。
Introduction: The limited value of TNM staging in locally advanced (LA) nasopharyngeal carcinoma (NPC), defined as stage III or IV NPC, highlights the need for prognostic markers. Here, we aimed to evaluate the ability of the cancer stem cell markers, BMI1, ALDH1, CD44, and CD24, and the epithelial-mesenchymal transition marker, vimentin, as novel prognostic markers in LA-NPC. Methods: A cohort of 83 patients with LA-NPC, previously recruited for another trial with a different goal, was used. The marker expression in tissue sections was evaluated using immunohistochemistry, and the association of expression with survival outcomes was analyzed using the Kaplan-Meier method and Cox regression analysis. Results: The expression of BMI1 and ALDH1 was not associated with survival. The tumoral expression of CD24, CD44, and vimentin was significantly associated with disease-free survival (DFS), whereas only the expression of CD24 was also significantly associated with overall survival (OS). Indeed, CD24 expression emerged as an independent prognostic factor as it was associated with survival in univariate and multivariate Cox regression analysis. Interestingly, combining the status of CD24 expression in tumor cells with the density of CD3 + tumor-infiltrating lymphocytes (TIL), a microenvironment/immune-related marker, identified a high-risk subgroup with the worst DFS and OS. Conclusions: These results suggest the utility of combining tumoral CD24 expression and the CD3 + TIL density as a prognostic factor in LA-NPC, with potential application in disease management and future trial design. Our findings also highlight the potential of combining immune- and cancer stem cell-related factors in personalized treatment strategies for cancer.
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