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Polysialic Acid Directs Tumor Cell Growth by Controlling Heterophilic Neural Cell Adhesion Molecule Interactions

机译:聚唾液酸通过控制嗜异性神经细胞粘附分子相互作用来指导肿瘤细胞的生长。

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Polysialic acid (PSA), a carbohydrate polymer attached to the neural cell adhesion molecule (NCAM), promotes neural plasticity and tumor malignancy, but its mode of action is controversial. Here we establish that PSA controls tumor cell growth and differentiation by interfering with NCAM signaling at cell-cell contacts. Interactions between cells with different PSA and NCAM expression profiles were initiated by enzymatic removal of PSA and by ectopic expression of NCAM or PSA-NCAM. Removal of PSA from the cell surface led to reduced proliferation and activated extracellular signal-regulated kinase (ERK), inducing enhanced survival and neuronal differentiation of neuroblastoma cells. Blocking with an NCAM-specific peptide prevented these effects. Combinatorial transinteraction studies with cells and membranes with different PSA and NCAM phenotypes revealed that heterophilic NCAM binding mimics the cellular responses to PSA removal. In conclusion, our data demonstrate that PSA masks heterophilic NCAM signals, having a direct impact on tumor cell growth. This provides a mechanism for how PSA may promote the genesis and progression of highly aggressive PSA-NCAM-positive tumors.
机译:聚唾液酸(PSA)是一种附着于神经细胞粘附分子(NCAM)的碳水化合物聚合物,可促进神经可塑性和肿瘤恶性程度,但其作用方式尚存争议。在这里,我们确定PSA通过干扰NCAM信号在细胞间的接触来控制肿瘤细胞的生长和分化。通过酶促去除PSA和异位表达NCAM或PSA-NCAM,可启动具有不同PSA和NCAM表达谱的细胞之间的相互作用。从细胞表面去除PSA导致增殖减少和活化的细胞外信号调节激酶(ERK),从而诱导成神经细胞瘤细胞提高生存率和神经元分化。用NCAM特异性肽封闭可防止这些影响。对具有不同PSA和NCAM表型的细胞和膜进行的组合交互研究表明,异源NCAM结合模拟了细胞对PSA去除的反应。总之,我们的数据表明PSA掩盖了异源性NCAM信号,对肿瘤细胞的生长具有直接影响。这为PSA如何促进高度侵袭性PSA-NCAM阳性肿瘤的发生和发展提供了一种机制。

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