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Lipid phosphate phosphatase-1 expression in cancer cells attenuates tumor growth and metastasis in mice

机译:癌细胞中脂质磷酸磷酸酶-1的表达减弱了小鼠的肿瘤生长和转移

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摘要

Lipid phosphate phosphatase-1 (LPP1) degrades lysophosphatidate (LPA) and attenuates receptor-mediated signaling. LPP1 expression is low in many cancer cells and tumors compared with normal tissues. It was hypothesized from studies with cultured cells that increasing LPP1 activity would decrease tumor growth and metastasis. This hypothesis has never been tested in vivo. To do this, we inducibly expressed LPP1 or a catalytically inactive mutant in cancer cells. Expressing active LPP1 increased extracellular LPA degradation by 5-fold. It also decreased the stimulation of Ca2+ transients by LPA, a nondephosphorylatable LPA1/2 receptor agonist and a protease-activated receptor-1 peptide. The latter results demonstrate that LPP1 has effects downstream of receptor activation. Decreased Ca2+ mobilization and Rho activation contributed to the effects of LPP1 in attenuating the LPA-induced migration of MDA-MB-231 breast cancer cells and their growth in 3D culture. Increasing LPP1 expression in breast and thyroid cancer cells decreased tumor growth and the metastasis by up to 80% compared with expression of inactive LPP1 or green fluorescent protein in syngeneic and xenograft mouse models. The present work demonstrates for the first time that increasing the LPP1 activity in three lines of aggressive cancer cells decreases their abilities to produce tumors and metastases in mice.
机译:脂质磷酸磷酸酶-1(LPP1)降解溶血磷脂酸酯(LPA),并减弱受体介导的信号传导。与正常组织相比,LPP1在许多癌细胞和肿瘤中的表达较低。从对培养细胞的研究中可以推测,增加LPP1活性将减少肿瘤的生长和转移。该假设从未在体内得到验证。为此,我们在癌细胞中诱导性表达了LPP1或催化失活的突变体。表达活性LPP1使细胞外LPA降解增加5倍。它也减少了LPA,不可去磷酸化的LPA1 / 2受体激动剂和蛋白酶激活的受体1肽对Ca 2 + 瞬变的刺激。后一结果证明LPP1在受体激活的下游具有作用。 Ca 2 + 动员的减少和Rho激活有助于LPP1减弱LPA诱导的MDA-MB-231乳腺癌细胞迁移及其在3D培养中的生长。在同基因和异种移植小鼠模型中,与无活性LPP1或绿色荧光蛋白的表达相比,乳腺癌和甲状腺癌细胞中LPP1表达的增加使肿瘤的生长和转移减少了80%。本工作首次证明增加三株侵袭性癌细胞中LPP1的活性会降低其在小鼠中产生肿瘤和转移的能力。

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