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C‐type natriuretic peptide in combination with sildenafil attenuates proliferation of rhabdomyosarcoma cells

机译:C型利钠肽结合西地那非可减缓横纹肌肉瘤细胞的增殖

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摘要

Rhabdomyosarcoma (RMS) is a malignant mesenchymal tumor and the most common soft tissue sarcoma in children. Because of several complications associated with intensive multimodal therapies, including growth disturbance and secondary cancer, novel therapies with less toxicity are urgently needed. C‐type natriuretic peptide (CNP), an endogenous peptide secreted by endothelial cells, exerts antiproliferative effects in multiple types of mesenchymal cells. Therefore, we investigated whether CNP attenuates proliferation of RMS cells. We examined RMS patient samples and RMS cell lines. All RMS clinical samples expressed higher levels of guanylyl cyclase B (GC‐B), the specific receptor for CNP, than RMS cell lines. GC‐B expression in RMS cells decreased with the number of passages in vitro. Therefore, GC‐B stable expression lines were established to mimic clinical samples. CNP increased cyclic guanosine monophosphate (cGMP) levels in RMS cells in a dose‐dependent manner, demonstrating the biological activity of style="fixed-case">CNP. However, because style="fixed-case">cGMP is quickly degraded by phosphodiesterases ( style="fixed-case">PDEs), the selective style="fixed-case">PDE5 inhibitor sildenafil was added to inhibit its degradation. In vitro, style="fixed-case">CNP, and sildenafil synergistically inhibited proliferation of style="fixed-case">RMS cells stably expressing style="fixed-case">GC‐B and decreased Raf‐1, Mitogen‐activated protein kinase kinase ( style="fixed-case">MEK), and extracellular signal‐regulated kinase ( style="fixed-case">ERK) phosphorylation. These results suggested that style="fixed-case">CNP in combination with sildenafil exerts antiproliferative effects on style="fixed-case">RMS cells by inhibiting the Raf/ style="fixed-case">MEK/ style="fixed-case">ERK pathway. This regimen exerted synergistic effects on tumor growth inhibition without severe adverse effects in vivo such as body weight loss. Thus, style="fixed-case">CNP in combination with sildenafil represents a promising new therapeutic approach against RMS.
机译:横纹肌肉瘤(RMS)是一种恶性间质瘤,是儿童中最常见的软组织肉瘤。由于与密集的多模式疗法有关的若干并发症,包括生长障碍和继发性癌症,迫切需要毒性更低的新疗法。 C型利钠肽(CNP)是内皮细胞分泌的一种内源性肽,在多种类型的间充质细胞中发挥抗增殖作用。因此,我们研究了CNP是否减弱RMS细胞的增殖。我们检查了RMS患者样品和RMS细胞系。与RMS细胞系相比,所有RMS临床样品均表达更高水平的鸟苷酰环化酶B(GC-B)(CNP的特异性受体)。 RMS细胞中的GC-B表达随着体外传代次数的减少而降低。因此,建立了GC-B稳定表达系来模拟临床样品。 CNP以剂量依赖性方式增加RMS细胞中环鸟苷单磷酸(cGMP)的水平,表明 style =“ fixed-case”> CNP 的生物活性。但是,由于 style =“ fixed-case”> cGMP 被磷酸二酯酶( style =“ fixed-case”> PDE s)迅速降解,因此选择性 style =“ fixed加入-case“> PDE 5抑制剂西地那非以抑制其降解。在体外, style =“ fixed-case”> CNP 和西地那非可协同抑制稳定表达 style =“ fixed- case“> GC -B和Raf-1下降,丝裂原激活的蛋白激酶激酶( style =” fixed-case“> MEK )和细胞外信号调节激酶( style =“ fixed-case”> ERK )磷酸化。这些结果表明, style =“ fixed-case”> CNP 与西地那非的组合可通过抑制Raf / 而对 style =“ fixed-case”> RMS 细胞产生抗增殖作用。 style =“ fixed-case”> MEK / style =“ fixed-case”> ERK 途径。该方案对肿瘤生长抑制具有协同作用,而在体内没有诸如体重减轻的严重不利影响。因此, style =“ fixed-case”> CNP 与西地那非的组合代表了一种有希望的针对RMS的新治疗方法。

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