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S100A16 的表达与接受根治性膀胱切除术的膀胱癌患者的生物学侵袭性和不良预后相关。

Expression of S100A16 Is Associated with Biological Aggressiveness and Poor Prognosis in Patients with Bladder Cancer Who Underwent Radical Cystectomy.

机构信息

Department of Urology, Kitasato University School of Medicine, 1-15-1 Kitasato, Minami-ku, Sagamihara 252-0374, Kanagawa, Japan.

Biofluid Biomarker Center, Niigata University, 8050 ikarashi 2-no-cho, Nishi-ku, Niigata 950-2181, Niigata, Japan.

出版信息

Int J Mol Sci. 2023 Sep 26;24(19):14536. doi: 10.3390/ijms241914536.

DOI:10.3390/ijms241914536
PMID:37833982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10572706/
Abstract

S100 calcium binding protein A16 (S100A16) is expressed in various cancers; however, there are few reports on S100A16 in bladder cancer (BC). We retrospectively investigated clinical data including clinicopathological features in 121 patients with BC who underwent radical cystectomy (RC). Immunohistochemical staining was performed to evaluate S100A16 expression in archived specimens. Cases with >5% expression and more than moderate staining intensity on cancer cells were considered positive. S100A16 expression was observed in 54 patients (44.6%). Univariate analysis showed that S100A16 expression was significantly associated with age, pT stage, recurrence, and cancer-specific death. Kaplan-Meier analyses showed that patients with S100A16 expression had shorter overall survival (OS), cancer-specific survival (CSS), and recurrence-free survival (RFS) than those without S100A16 expression. In multivariate analysis, pT stage was an independent prognostic factor for OS and lymph node metastasis for CSS and RFS. S100A16 expression may be a biomarker of a biologically aggressive phenotype and poor prognosis in patients with BC who underwent RC. The PI3k/Akt signaling pathway is probably associated with S100A16 and may be a therapeutic target.

摘要

S100 钙结合蛋白 A16(S100A16)在各种癌症中表达;然而,关于膀胱癌(BC)中 S100A16 的报道很少。我们回顾性调查了 121 例接受根治性膀胱切除术(RC)的 BC 患者的临床资料,包括临床病理特征。对存档标本进行免疫组织化学染色,以评估 S100A16 的表达。将癌细胞中表达>5%和中度以上染色强度的病例视为阳性。在 54 例患者(44.6%)中观察到 S100A16 表达。单因素分析显示,S100A16 表达与年龄、pT 分期、复发和癌症特异性死亡显著相关。Kaplan-Meier 分析显示,S100A16 表达的患者总生存期(OS)、癌症特异性生存期(CSS)和无复发生存期(RFS)均短于无 S100A16 表达的患者。多因素分析显示,pT 分期是 OS 的独立预后因素,淋巴结转移是 CSS 和 RFS 的独立预后因素。S100A16 表达可能是 RC 后 BC 患者具有侵袭性生物学表型和不良预后的生物标志物。PI3k/Akt 信号通路可能与 S100A16 相关,可能是治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/748d/10572706/ef869167b54c/ijms-24-14536-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/748d/10572706/8aeebc58c1de/ijms-24-14536-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/748d/10572706/ef869167b54c/ijms-24-14536-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/748d/10572706/8aeebc58c1de/ijms-24-14536-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/748d/10572706/ef869167b54c/ijms-24-14536-g002a.jpg

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