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一种用于癌症微小残留病病例中亚宏观转移灶可视化的原创方法。

An original method for submacroscopic metastases visualization in cases of cancer minimal residual disease.

作者信息

Le Pape A, Barot-Ciorbaru R, Musset M, Baulieu J L, Jubault C, Lemarié E, Pourcelot L, Besnard J C, Nicolau C, Mathé G

出版信息

Biomed Pharmacother. 1986;40(10):392-8.

PMID:3580508
Abstract

Scintigraphic imaging due to its sensitivity is in many cases one of the most powerful techniques for demonstrating metastases. Severe limitations still exist in cancer when it is necessary to detect the presence of a few tumour cells in the residual minimal disease. In preliminary experiments it had been observed that an immunomodulator isolated from Nocardia bacteria (Nocardia Soluble Peptidoglycan Derivative: NSPD) electively bound to a model of activated macrophages. An hypothesis has been put forward that the enhanced detection of macrophages that are usually present in the vicinity or inside tumours should represent a polyspecific test for scintigraphy of a variety of metastases. NSPD radiolabelled with 99mTechnetium is not usable when injected intravenously due to its physiochemical properties. It has therefore been encapsulated into liposomes then administered via the respiratory tract as an aerosol. Amphiphilic properties, as well as its low molecular weight allow a rapid diffusion of NSPD in blood. Scintigraphy of metastases was possible from 1.5 to 6 hours after inhalation. The first stage of the study was carried out on 5 patients bearing known metastases (skin, lymph nodes, bone) from malignant melanoma that all were imaged with 99mTc-NSPD. The test was then applied to patients with a high risk of recurrent cancers (melanoma: 6, breast tumour: 7) based on the detection in their plasmas of high Lipid Associated Sialic Acid (LASA) concentrations. The association of these two sensitive techniques has resulted in the detection of very small metastases that were not seen using conventional scintigraphy; they were then confirmed histologically.

摘要

由于其敏感性,闪烁成像在许多情况下是显示转移灶最有效的技术之一。在癌症中,当需要在残留的微小病灶中检测少量肿瘤细胞时,仍然存在严重的局限性。在初步实验中,观察到从诺卡氏菌分离出的一种免疫调节剂(诺卡氏菌可溶性肽聚糖衍生物:NSPD)选择性地结合到活化巨噬细胞模型上。有人提出一个假说,即增强对通常存在于肿瘤附近或内部的巨噬细胞的检测,应该代表一种用于多种转移灶闪烁成像的多特异性检测方法。由于其物理化学性质,用99m锝标记的NSPD静脉注射时不可用。因此,它被包裹在脂质体中,然后作为气雾剂通过呼吸道给药。两亲性以及其低分子量使得NSPD能在血液中快速扩散。吸入后1.5至6小时可进行转移灶的闪烁成像。研究的第一阶段对5名患有已知恶性黑色素瘤转移灶(皮肤、淋巴结、骨)的患者进行,所有患者均用99mTc-NSPD进行成像。然后,基于在血浆中检测到高浓度的脂质相关唾液酸(LASA),将该检测应用于具有癌症复发高风险的患者(黑色素瘤:6例,乳腺肿瘤:7例)。这两种敏感技术的联合使用导致检测到了使用传统闪烁成像未发现的非常小的转移灶;随后经组织学证实。

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