CRISPR/Cas9-mediated knock out of ITGB6 in human OSCC cells reduced migration and proliferation ability.

IF 2.4 2区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE Head & Face Medicine Pub Date : 2024-06-18 DOI:10.1186/s13005-024-00437-x
Maximilian Geyer, Fabian Geyer, Ute Reuning, Sarah Klapproth, Klaus-Dietrich Wolff, Markus Nieberler
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Abstract

Background: The treatment of oral squamous cell carcinoma (OSCC) remains challenging and survival rates have not been improved significantly over the past decades. Integrins have been recognized driving the cancer progression and high expression levels cause poor outcomes in patients afflicted with OSCC. Integrin αvβ6 and its subunit integrin beta 6 (ITGB6) were discovered to enhance the invasiveness by providing beneficial effects on downstream pathways promoting the cancer progression. The objective of this study was to establish a CRISPR/Cas9-mediated knock out of ITGB6 in the human OSCC cell line HN and investigate the effects on the migration and proliferation ability.

Methods: ITGB6 knock out was performed using the CRISPR/Cas9-system, RNPs, and lipofection. Monoclonal cell clones were achieved by limiting dilution and knock out verification was carried out by sanger sequencing and FACS on protein level. The effects of the knock out on the proliferation and migration ability were evaluated by using MTT and scratch assays. In addition, in silico TCGA analysis was utilized regarding the effects of ITGB6 on overall survival and perineural invasion.

Results: In silico analysis revealed a significant impact of ITGB6 mRNA expression levels on the overall survival of patients afflicted with OSCC. Additionally, a significantly higher rate of perineural invasion was discovered. CRISPR/Cas9-mediated knock out of ITGB6 was performed in the OSCC cell line HN, resulting in the generation of a monoclonal knock out clone. The knock out clone exhibited a significantly reduced migration and proliferation ability when compared to the wildtype.

Conclusions: ITGB6 is a relevant factor in the progression of OSCC and can be used for the development of novel treatment strategies. The present study is the first to establish a monoclonal CRISPR/Cas9-mediated ITGB6 knockout cell clone derived from an OSCC cell line. It suggests that ITGB6 has a significant impact on the proliferative and migratory capacity in vitro.

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CRISPR/Cas9 介导的人 OSCC 细胞 ITGB6 基因敲除降低了迁移和增殖能力。
背景:口腔鳞状细胞癌(OSCC)的治疗仍然充满挑战,在过去几十年中,生存率一直没有显著提高。整合素被认为是癌症进展的驱动因素,高表达水平导致 OSCC 患者预后不佳。研究发现,整合素αvβ6及其亚基整合素β6(ITGB6)可通过对促进癌症进展的下游通路产生有益影响来增强侵袭性。本研究的目的是在人OSCC细胞系HN中建立CRISPR/Cas9介导的ITGB6基因敲除,并研究其对迁移和增殖能力的影响:方法:利用CRISPR/Cas9系统、RNPs和脂质感染技术敲除ITGB6。方法:利用 CRISPR/Cas9 系统、RNPs 和脂质体感染技术进行 ITGB6 基因敲除,通过限制稀释获得单克隆细胞克隆,并通过桑格测序和 FACS 在蛋白质水平上对基因敲除进行验证。通过 MTT 和划痕试验评估了基因敲除对细胞增殖和迁移能力的影响。此外,还就ITGB6对总存活率和神经周围侵袭的影响进行了TCGA硅学分析:硅学分析显示,ITGB6 mRNA表达水平对OSCC患者的总生存率有显著影响。此外,研究还发现ITGB6的神经周围侵袭率明显较高。在 OSCC 细胞系 HN 中进行了 CRISPR/Cas9 介导的 ITGB6 基因敲除,从而产生了一个单克隆基因敲除克隆。与野生型相比,基因敲除克隆的迁移和增殖能力明显降低:ITGB6是OSCC进展的一个相关因素,可用于开发新型治疗策略。本研究首次从OSCC细胞系中建立了单克隆CRISPR/Cas9介导的ITGB6基因敲除细胞克隆。研究表明,ITGB6对体外增殖和迁移能力有显著影响。
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来源期刊
Head & Face Medicine
Head & Face Medicine DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
4.70
自引率
3.30%
发文量
32
审稿时长
>12 weeks
期刊介绍: Head & Face Medicine is a multidisciplinary open access journal that publishes basic and clinical research concerning all aspects of cranial, facial and oral conditions. The journal covers all aspects of cranial, facial and oral diseases and their management. It has been designed as a multidisciplinary journal for clinicians and researchers involved in the diagnostic and therapeutic aspects of diseases which affect the human head and face. The journal is wide-ranging, covering the development, aetiology, epidemiology and therapy of head and face diseases to the basic science that underlies these diseases. Management of head and face diseases includes all aspects of surgical and non-surgical treatments including psychopharmacological therapies.
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