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Ubiquitin C‐terminal hydrolase‐L1 has prognostic relevance and is a therapeutic target for high‐grade neuroendocrine lung cancers

机译:泛素C末端水解酶L1具有预后相关性是高度神经内分泌肺癌的治疗靶标

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摘要

High‐grade neuroendocrine lung cancer (HGNEC), which includes small cell lung cancer (SCLC) and large cell neuroendocrine carcinoma (LCNEC) of the lung is a rapidly proliferating, aggressive form of lung cancer. The initial standard chemotherapeutic regimens of platinum doublets are recommended for SCLC and have been frequently used for LCNEC. However, there are currently no molecularly targeted agents with proven clinical benefit for this disease. The deubiquitinating enzyme ubiquitin C‐terminal hydrolase‐L1 (UCHL1) is a neuroendocrine cell‐specific product that is known as a potential oncogene in several types of cancer, but little is known about the biological function of UCHL1 and its therapeutic potential in HGNEC. In this study, we found that preclinical efficacy evoked by targeting UCHL1 was relevant to prognosis in HGNEC. UCHL1 was found to be expressed in HGNEC, particularly in cell lines and patient samples of SCLC, and the combined use of platinum doublets with selective UCHL1 inhibitors improved its therapeutic response in vitro. Immunohistochemical expression of UCHL1 was significantly associated with postoperative survival in patients with HGNEC and contributed towards distinguishing SCLC from LCNEC. Circulating extracellular vesicles (EV), including exosomes isolated from lung cancer cell lines and serum from early‐stage HGNEC, were verified by electron microscopy and nanoparticle tracking analysis. Higher levels of UCHL1 mRNA in EV were found in the samples of patients with early‐stage HGNEC than those with early‐stage NSCLC and healthy donors’ EV. Taken together, UCHL1 may be a potential prognostic marker and a promising druggable target for HGNEC.
机译:高级肺内分泌性肺癌(HGNEC),包括小细胞肺癌(SCLC)和大细胞神经内分泌癌(LCNEC),是一种迅速扩散的侵袭性肺癌。对于SCLC,建议使用铂双峰的初始标准化学治疗方案,并经常用于LCNEC。但是,目前尚无分子靶向药物对这种疾病具有证明的临床益处。去泛素化酶泛素C末端水解酶L1(UCHL1)是一种神经内分泌细胞特异性产物,在几种类型的癌症中被称为潜在的癌基因,但对UCHL1的生物学功能及其在HGNEC中的治疗潜力知之甚少。在这项研究中,我们发现靶向UCHL1引起的临床前疗效与HGNEC的预后有关。发现UCHL1在HGNEC中表达,特别是在细胞系和SCLC患者样品中表达,铂双峰与选择性UCHL1抑制剂的联合使用改善了其体外治疗反应。 UCHL1的免疫组织化学表达与HGNEC患者的术后生存率显着相关,并有助于区分SCLC和LCNEC。循环的细胞外囊泡(EV),包括从肺癌细胞系分离的外泌体和早期HGNEC的血清,已通过电子显微镜和纳米粒子跟踪分析进行了验证。早期HGNEC患者的样本中EV中的UCHL1 mRNA水平高于早期NSCLC和健康供体EV的患者。综上所述,UCHL1可能是HGNEC的潜在预后标志物和有希望的药物靶标。

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