食管鳞状细胞癌患者血清和组织 SIRT1 水平的相关性

Cancer diagnosis & prognosis Pub Date : 2024-11-03 eCollection Date: 2024-11-01 DOI:10.21873/cdp.10393
Hiroki Morishita, Ryota Otsuka, Takeshi Toyozumi, Yasunori Matsumoto, Nobufumi Sekino, Koichiro Okada, Tadashi Shiraishi, Toshiki Kamata, Shinichiro Iida, Tenshi Makiyama, Yuri Nishioka, Masanari Yamada, Hisahiro Matsubara
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引用次数: 0

摘要

背景/目的:确定作为食管鳞状细胞癌(ESCC)治疗靶点的预后和分子标记物可提高多学科治疗的疗效。虽然sirtuin 1(SIRT1)的组织表达与ESCC的肿瘤进展有关,但血清SIRT1水平的预后意义及其与组织SIRT1的相关性仍未得到探讨。本研究旨在探讨 ESCC 患者血清和组织 SIRT1 水平之间的相关性:本研究共招募了 38 名术前未接受治疗的 ESCC 患者。手术标本中的 SIRT1 表达通过免疫染色法进行评估,血清中的 SIRT1 水平则通过酶联免疫吸附试验进行测定。我们分析了组织和血清 SIRT1 水平、临床病理特征和患者预后之间的关联:结果:组织中 SIRT1 的阳性表达与肿瘤深度明显相关(p=0.020)。它还与较差的总生存期(OS)和无复发生存期(RFS)明显相关(分别为 p=0.041 和 p=0.012)。血清 SIRT1 水平升高与肿瘤深度增加和体重减轻显著相关(p=0.012 和 p=0.030)。虽然较高的血清 SIRT1 水平往往与较差的 OS 相关(p=0.069),但在组织中的 SIRT1 表达与其在血清中的浓度之间没有发现明显的相关性:结论:SIRT1组织表达可能是ESCC有价值的预后标志物。结论:SIRT1 组织表达可能是 ESCC 有价值的预后标志物,但血清 SIRT1 水平的临床意义似乎与其组织表达不同。未来的研究需要明确血清 SIRT1 在 ESCC 中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation Between Serum and Tissue SIRT1 Levels in Patients With Esophageal Squamous Cell Carcinoma.

Background/aim: Identifying prognostic and molecular markers as therapeutic targets for esophageal squamous cell carcinoma (ESCC) could enhance the efficacy of multidisciplinary treatments. While tissue expression of sirtuin 1 (SIRT1) has been linked to tumor progression in ESCC, prognostic significance of serum SIRT1 levels and their correlation with tissue SIRT1 remains unexplored. This study aimed to investigate the correlation between serum and tissue SIRT1 levels in patients with ESCC.

Patients and methods: A total of 38 patients diagnosed with ESCC who were untreated preoperatively were recruited for this study. SIRT1 expression in the surgical specimens was assessed through immunostaining, while serum SIRT1 levels were measured using an enzyme-linked immunosorbent assay. We analyzed the association between tissue and serum SIRT1 levels, clinicopathological features, and patient prognosis.

Results: Positive SIRT1 expression in tissue was significantly associated with deeper tumor depth (p=0.020). It was also significantly associated with poorer overall survival (OS) and relapse-free survival (RFS) (p=0.041 and p=0.012, respectively). Elevated serum SIRT1 levels were significantly correlated with increased tumor depth and weight loss (p=0.012 and p=0.030). While higher serum SIRT1 levels tended to be associated with poorer OS (p=0.069), no significant correlation was found between SIRT1 expression in tissue and its concentration in serum.

Conclusion: SIRT1 tissue expression may be a valuable prognostic marker in ESCC. However, the clinical significance of serum SIRT1 levels appears to differ from that of its tissue expression. Future research is required to clarify the role of serum SIRT1 in ESCC.

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