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首页> 外文期刊>BMC Cancer >GR, Sgk1, and NDRG1 in esophageal squamous cell carcinoma: their correlation with therapeutic outcome of neoadjuvant chemotherapy
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GR, Sgk1, and NDRG1 in esophageal squamous cell carcinoma: their correlation with therapeutic outcome of neoadjuvant chemotherapy

机译:食管鳞状细胞癌中的GR,SGK1和NDRG1:它们与Neoadjuvant化疗的治疗结果相关

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BACKGROUND:Esophageal squamous cell carcinoma (ESCC) is a highly malignant neoplasm. The glucocorticoid (GC)-glucocorticoid receptor (GR) pathway plays pivotal roles in cellular response to various stresses of tumor cells, including chemotherapy. However, the status of the GC-GR pathway in ESCC, including its correlation with chemotherapeutic responses, is largely unknown.METHODS:GR, serum-and glucocorticoid-regulated kinase 1 (Sgk1), and N-myc down regulation gene 1 (NDRG1) were immunolocalized in 98 patients with ESCC who had undergone esophagectomy following neoadjuvant chemotherapy (NAC) with 2 courses of 5-fluorouracil + cisplatin. We also examined biopsy specimens before NAC in 42 cases and compared the results between those before and after NAC.RESULTS:Overall survival (OS) of the patients treated with surgery following NAC was significantly shorter in the group with high GR than that with low GR status (P?=?0.0473). Both OS and disease-free survival (DFS) were significantly shorter in both Sgk1- and NDRG1-high groups than in the low groups (OS: Sgk1, P?=?0.0055; NDRG1, P?=?0.0021; DFS: Sgk1, P?=?0.0240; NDRG1, P?=?0.0086). Biopsy specimens before NAC showed significantly shorter DFS in the high Sgk1 group (P?=?0.0095), while both OS and DFS were shorter in the high NDRG1 group (OS, P?=?0.0233; DFS, P?=?0.0006) than in the respective low groups. In the high NDRG1 group of biopsy specimens before NAC, the tumor reduction rate by NAC was significantly attenuated (P?=?0.021).CONCLUSIONS:High GR, Sgk1, and NDRG1 statuses in ESCC after NAC was significantly associated with an overall worse prognosis, with no significant changes in their expression levels before and after NAC. Therefore, increased activity of the GC-GR pathway with enhanced induction of Sgk1 and NDRG1 in carcinoma cells play pivotal roles in tumor progression and development of chemo-resistance in patients with ESCC undergoing NAC.
机译:背景:食管鳞状细胞癌(ESCC)是一种高度恶性肿瘤。糖皮质激素(GC) - 葡糖皮质激素受体(GR)途径在细胞反应中起枢转作用对肿瘤细胞的各种应力,包括化学疗法。然而,ESCC中GC-GR途径的状态,包括其与化学治疗反应的相关性,主要是未知的。方法:GR,血清和糖皮质激素调节激酶1(SGK1)和N-MYC下调基因1(NDRG1 )在98例ESCC患者中免疫悬垂的,患有Neoadjuvant化疗(NAC)后的食管切除术(NAC),其中2种5氟尿嘧啶+顺铂。我们还在NAC之前检查了活组织检查标本42例,并将结果与​​NAC.Results之前和之后的结果进行了比较状态(p?= 0.0473)。 SGK1和NDRG1高组中的OS和无病生存(DFS)显着短,而不是低组(OS:SGK1,P?= 0.0055; NDRG1,P?= 0.0021; DFS:SGK1, p?= 0.0240; NDRG1,P?= 0.0086)。 NAC之前的活组织检查标本在高SGK1组中显示出明显较短的DFS(P?= 0.0095),而OS和DF在高NDRG1组中较短(OS,P?= 0.0233; DFS,P?0.0006)而不是在各个低群体中。在NAC之前的高NDRG1组活检标本中,NAC的肿瘤减少率显着减弱(P?= 0.021)。NAC后ESCC中的高GR,SGK1和NDRG1状态明显与总体上更差的预后相关,NAC之前和之后的表达水平没有显着变化。因此,GC-GR通路的活性增加了Carcinoma细胞中SGK1和NDRG1的增强诱导的活性在肿瘤进展和ESCC患者中进行肿瘤进展和开发ESCC患者的抗性。

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