CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The different prognostic significance of polysialic acid and CD56 expression in tumor cells and lymphocytes identified in breast cancer.
The different prognostic significance of polysialic acid and CD56 expression in tumor cells and lymphocytes identified in breast cancer.
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蛋白质糖基化是将碳水化合物连接至蛋白质的基本过程,会改变蛋白质的生物学活性。糖基化状态改变与包括乳腺癌在内的多种癌症相关。通过对乳腺癌患者肿瘤进行免疫组织学分析,我们发现乳腺癌中存在一种非典型糖链——多聚唾液酸(polySia)。
值得注意的是,polySia不仅表达于肿瘤细胞,也表达于TIL(肿瘤浸润淋巴细胞);研究还显示ST8Sia4是主要表达的多聚唾液酸转移酶。分析肿瘤细胞ST8Sia4表达后发现,高表达与患者结局较差相关,而浸润性基质细胞中ST8Sia4表达则与较好结局相关。
我们进一步研究已知可发生多聚唾液酸化的CD56蛋白,在乳腺肿瘤细胞和TIL上均发现CD56及polySia表达。除HER2表达的患者肿瘤外,CD56表达与polySia表达无正相关。在HER2表达肿瘤中,CD56表达与HER2表达评分显著相关。评估肿瘤细胞CD56表达发现,其与患者结局较差显著相关。相反,TIL上的CD56表达与较好临床结局显著相关。CD56+ TIL阳性肿瘤也始终检测到polySia+ TIL。有趣的是,在TIL的CD56低表达或阴性肿瘤中,仍可识别出polySia+淋巴细胞群,且这类淋巴细胞与不良预后相关。
总之,本研究首次详细报告乳腺癌中的polySia和CD56,并显示其预后意义取决于肿瘤内表达的细胞类型。
Protein glycosylation, the attachment of carbohydrates onto proteins, is a fundamental process that alters the biological activity of proteins. Changes to glycosylation states are associated with many forms of cancer including breast cancer. Through immunohistological analysis of breast cancer patient tumors, we have discovered the expression of an atypical glycan-polysialic acid (polySia)-in breast cancer.
Notably, we have identified polySia expression in not only tumor cells but also on tumor-infiltrating lymphocytes (TILs) and our study reveals ST8Sia4 as the predominant polysialyltransferase expressed. Evaluation of ST8Sia4 expression in tumor cells identified an association between high expression levels and poor patient outcomes whereas ST8Sia4 expression in infiltrating stromal cells was associated with good patient outcomes. Investigation into CD56, a protein known to be polysialylated, found CD56 and polySia expression on breast tumor cells and TILs. CD56 expression did not positively correlate with polySia expression except in patient tumors which expressed HER2.
In these HER2 expressing tumors, CD56 expression was significantly associated with HER2 expression score. Evaluation of CD56 tumor cell expression identified a significant association between CD56 expression and poor patient outcomes. By contrast, CD56 expression on TILs was significantly associated with good clinical outcomes.
Tumors with CD56+ TILs were also consistently polySia TIL positive. Interestingly, in tumors where TILs were CD56 low-to-negative, a polySia+ lymphocyte population was still identified and the presence of these lymphocytes was a poor prognostic indicator.
Overall, this study provides the first detailed report of polySia and CD56 in breast cancer and demonstrates that the prognostic significance is dependent on the cell type expression within the tumor.
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