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Group IIa secretory phospholipase expression correlates with group IIa secretory phospholipase inhibition–mediated cell death in K-ras mutant lung cancer cells

机译:与Ⅱa族分泌型磷脂酶抑制介导的细胞死亡Ⅱa族分泌型磷脂酶表达相关的K-ras突变的肺癌细胞

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摘要

ObjectiveThere are currently no targeted therapies against lung tumors with oncogenic K-ras mutations that are found in 25% to −40% of lung cancers and are characterized by their resistance to epidermal growth factor receptor inhibitors. The isozyme group IIa secretory phospholipase A2 (sPLA2IIa) is a potential biomarker and regulator of lung cancer cell invasion; however, the relationship between K-ras mutations and sPLA2IIa has yet to be investigated. We hypothesize that sPLA2IIa modulates lung cancer cell growth in K-ras mutant cells and that sPLA2IIa expression in human lung tumors is increased in K-ras mutant tumors.
机译:目的目前尚无针对具有致癌性K-ras突变的肺癌的靶向疗法,这种疗法在25%至-40%的肺癌中发现,其特征在于它们对表皮生长因子受体抑制剂的耐药性。同功酶IIa分泌型磷脂酶A2(sPLA2IIa)是肺癌细胞侵袭的潜在生物标志物和调节剂。然而,K-ras突变与sPLA2IIa之间的关系尚待研究。我们假设sPLA2IIa调节K-ras突变细胞中的肺癌细胞生长,并且在人肺肿瘤中sPLA2IIa的表达在K-ras突变肿瘤中增加。

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