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The phosphorylation status of VASP at serine 322 can be predictive for aggressiveness of invasive ductal carcinoma

机译:VASP在322位丝氨酸的磷酸化状态可预测浸润性导管癌的侵袭性。

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摘要

Vasodilator-stimulated phosphoprotein (VASP) signaling is critical for dynamic actin reorganization processes that define the motile phenotype of cells. Here we show that VASP is generally highly expressed in normal breast tissue and breast cancer. We also show that the phosphorylation status of VASP at S322 can be predictive for breast cancer progression to an aggressive phenotype. Our data indicate that phosphorylation at S322 is gradually decreased from normal breast to DCIS, luminal/ER+, HER2+ and basal-like/TN phenotypes. Similarly, the expression levels of PKD2, the kinase that phosphorylates VASP at this site, are decreased in invasive ductal carcinoma samples of all three groups. Overall, the phosphorylation status of this residue may serve as an indicator of aggressiveness of breast tumors.
机译:血管舒张剂刺激的磷蛋白(VASP)信号对于动态肌动蛋白重组过程(定义细胞的运动表型)至关重要。在这里,我们显示VASP通常在正常的乳腺组织和乳腺癌中高表达。我们还显示,在S322处VASP的磷酸化状态可以预测乳腺癌进展为侵​​袭性表型。我们的数据表明,S322处的磷酸化水平从正常乳腺逐渐降低至DCIS,管腔/ ER +,HER2 +和基底样/ TN表型。同样,在这三组浸润性导管癌样本中,PKD2(在该位点使VASP磷酸化的激酶)的表达水平降低。总的来说,该残基的磷酸化状态可以作为乳腺肿瘤侵袭性的指标。

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