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表皮生长因子受体(EGFR)密度可能并非人头颈癌细胞系中EGFR靶向光免疫疗法疗效的唯一决定因素。

Epidermal growth factor receptor (EGFR) density may not be the only determinant for the efficacy of EGFR-targeted photoimmunotherapy in human head and neck cancer cell lines.

作者信息

Peng Wei, de Bruijn Henriette S, Farrell Eric, Sioud Mouldy, Mashayekhi Vida, Oliveira Sabrina, van Dam Go M, Roodenburg Jan L N, Witjes Max J H, Robinson Dominic J

机构信息

Department of Oral and Maxillofacial Surgery, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Department of Otorhinolaryngology and Head and Neck Surgery, Center for Optical Diagnostics and Therapy, Erasmus Medical Center, Rotterdam, The Netherlands.

出版信息

Lasers Surg Med. 2018 Jul;50(5):513-522. doi: 10.1002/lsm.22930. Epub 2018 May 19.

Abstract

OBJECTIVE

The aim of this study was to investigate the effects of targeted photoimmunotherapy (PIT) in vitro on cell lines with various expression levels of epidermal growth factor receptor (EGFR) using an anti-EGFR targeted conjugate composed of Cetuximab and IR700DX, phthalocyanine dye.

MATERIALS AND METHODS

Relative EGFR density and cell binding assay was conducted in three human head & neck cancer cell lines (scc-U2, scc-U8, and OSC19) and one reference cell line A431. After incubation with the conjugate for 1 or 24 hours, cellular uptake and localization were investigated by confocal laser scanning microscopy and quantified by image analysis. Cell survival was determined using the MTS assay and alamarBlue assay after PIT with a 690 nm laser to a dose of 7 J.cm (at 5 mW.cm ). The mode of cell death was examined with flow cytometry using apoptosis/necrosis staining by Annexin V/propidium iodide, together with immunoblots of anti-apoptotic Bcl-2 family proteins Bcl-2 and Bcl-xL.

RESULTS

A431 cells had the highest EGFR density followed by OSC19, and then scc-U2 and scc-U8. The conjugates were localized both on the surface and in the cytosol of the cells after 1- and 24-hour incubation. After 24-hour incubation the granular pattern was more pronounced and in a similar pattern of a lysosomal probe, suggesting that the uptake of conjugates by cells was via receptor-mediated endocytosis. The results obtained from the quantitative imaging analysis correlate with the level of EGFR expression. Targeted PIT killed scc-U8 and A431 cells efficiently; while scc-U2 and OSC19 were less sensitive to this treatment, despite having similar EGFR density, uptake and localization pattern. Scc-U2 cells showed less apoptotic cell dealth than in A431 after 24-hour targeted PIT. Immunoblots showed significantly higher expression of anti-apoptotic Bcl-2 and Bcl-xL proteins in scc-U2 cell lines compared to scc-U8.

CONCLUSION

Our study suggests that the effectiveness of EGFR targeted PIT is not only dependent upon EGFR density. Intrinsic biological properties of tumor cell lines also play a role in determining the efficacy of targeted PIT. We have shown that in scc-U2 cells this difference may be caused by differences in the apoptopic pathway. Lasers Surg. Med. 50:513-522, 2018. © 2018 Wiley Periodicals, Inc.

摘要

目的

本研究旨在使用由西妥昔单抗和酞菁染料IR700DX组成的抗表皮生长因子受体(EGFR)靶向偶联物,在体外研究靶向光免疫疗法(PIT)对具有不同EGFR表达水平的细胞系的影响。

材料与方法

在三种人头颈部癌细胞系(scc-U2、scc-U8和OSC19)和一种对照细胞系A431中进行相对EGFR密度和细胞结合试验。与偶联物孵育1或24小时后,通过共聚焦激光扫描显微镜研究细胞摄取和定位,并通过图像分析进行定量。用690nm激光以7J.cm(5mW.cm)的剂量进行PIT后,使用MTS试验和alamarBlue试验测定细胞存活率。通过Annexin V/碘化丙啶凋亡/坏死染色的流式细胞术以及抗凋亡Bcl-2家族蛋白Bcl-2和Bcl-xL的免疫印迹检查细胞死亡模式。

结果

A431细胞的EGFR密度最高,其次是OSC19,然后是scc-U2和scc-U8。孵育1小时和24小时后,偶联物定位于细胞表面和细胞质中。孵育24小时后,颗粒状模式更明显,且与溶酶体探针的模式相似,表明细胞对偶联物的摄取是通过受体介导的内吞作用。定量成像分析得到的结果与EGFR表达水平相关。靶向PIT有效杀死scc-U8和A431细胞;而scc-U2和OSC19对这种治疗不太敏感,尽管它们具有相似的EGFR密度、摄取和定位模式。24小时靶向PIT后,scc-U2细胞的凋亡细胞死亡比A431细胞少。免疫印迹显示,与scc-U8相比,scc-U2细胞系中抗凋亡Bcl-2和Bcl-xL蛋白的表达明显更高。

结论

我们的研究表明,EGFR靶向PIT的有效性不仅取决于EGFR密度。肿瘤细胞系的内在生物学特性在确定靶向PIT的疗效方面也起作用。我们已经表明,在scc-U2细胞中,这种差异可能是由凋亡途径的差异引起的。激光外科与医学。50:513 - 522,2018。©2018威利期刊公司。

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