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Calcium and calcium sensing receptor modulates the expression of thymidylate synthase NAD(P)H:quinone oxidoreductase 1 and survivin in human colon carcinoma cells: promotion of cytotoxic response to mitomycin C and fluorouracil

机译:钙和钙敏感受体调节人结肠癌细胞中胸苷酸合酶NAD(P)H:醌氧化还原酶1和survivin的表达:促进对丝裂霉素C和氟尿嘧啶的细胞毒性反应

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摘要

Ca2+ and the cell-surface calcium sensing receptor (CaSR) constitute a novel and robust ligand/receptor system in regulating the proliferation and differentiation of colonic epithelial cells. Here we show that activation of CaSR by extracellular Ca2+ (or CaSR agonists) enhanced the sensitivity of human colon carcinoma cells to mitomycin C (MMC) and fluorouracil (5-FU). Activation of CaSR up-regulated the expression of MMC activating enzyme, NAD(P)H:quinone oxidoreductase 1 (NQO-1) and down-regulated the expression of 5-FU target, thymidylate synthase (TS) and the anti-apoptotic protein survivin. Cells that were resistant to drugs expressed little or no CaSR but abundant amount of survivin. Disruption of CaSR expression by shRNA targeting the CaSR abrogated these modulating effects of CaSR activation on the expression of NQO1, TS, survivin and cytotoxic response to drugs. It is concluded that activation of CaSR can enhance colon cancer cell sensitivity to MMC and 5-FU and can modulate the expression of molecules involved in the cellular responses to these cytotoxic drugs.
机译:Ca 2 + 和细胞表面钙敏感受体(CaSR)构成了一种新颖而强大的配体/受体系统,可调节结肠上皮细胞的增殖和分化。在这里,我们表明细胞外Ca 2 + (或CaSR激动剂)对CaSR的激活增强了人结肠癌细胞对丝裂霉素C(MMC)和氟尿嘧啶(5-FU)的敏感性。 CaSR的激活上调了MMC激活酶,NAD(P)H:醌氧化还原酶1(NQO-1)的表达,并下调了5-FU靶标,胸苷酸合酶(TS)和抗凋亡蛋白的表达。 survivin。对药物有抗性的细胞表达很少或不表达CaSR,但表达大量的Survivin。靶向CaSR的shRNA破坏了CaSR的表达,从而消除了CaSR激活对NQO1,TS,存活蛋白和药物的细胞毒性反应的调控作用。结论是,CaSR的激活可以增强结肠癌细胞对MMC和5-FU的敏感性,并可以调节参与细胞对这些细胞毒性药物的反应的分子的表达。

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