Evaluating ECM stiffness and liver cancer radiation response via shear-wave elasticity in 3D culture models.

IF 3.3 2区 医学 Q2 ONCOLOGY Radiation Oncology Pub Date : 2024-09-27 DOI:10.1186/s13014-024-02513-7
Shao-Lun Lu, Yu Pei, Wei-Wen Liu, Kun Han, Jason Chia-Hsien Cheng, Pai-Chi Li
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Abstract

Background: The stiffness of the tumor microenvironment (TME) directly influences cellular behaviors. Radiotherapy (RT) is a common treatment for solid tumors, but the TME can impact its efficacy. In the case of liver cancer, clinical observations have shown that tumors within a cirrhotic, stiffer background respond less to RT, suggesting that the extracellular matrix (ECM) stiffness plays a critical role in the development of radioresistance.

Methods: This study explored the effects of ECM stiffness and the inhibition of lysyl oxidase (LOX) isoenzymes on the radiation response of liver cancer in a millimeter-sized three-dimensional (3D) culture. We constructed a cube-shaped ECM-based millimeter-sized hydrogel containing Huh7 human liver cancer cells. By modulating the collagen concentration, we produced two groups of samples with different ECM stiffnesses to mimic the clinical scenarios of normal and cirrhotic livers. We used a single-transducer system for shear-wave-based elasticity measurement, to derive Young's modulus of the 3D cell culture to investigate how the ECM stiffness affects radiosensitivity. This is the first demonstration of a workflow for assessing radiation-induced response in a millimeter-sized 3D culture.

Results: Increased ECM stiffness was associated with a decreased radiation response. Moreover, sonoporation-assisted LOX inhibition with BAPN (β-aminopropionitrile monofumarate) significantly decreased the initial ECM stiffness and increased RT-induced cell death. Inhibition of LOX was particularly effective in reducing ECM stiffness in stiffer matrices. Combining LOX inhibition with RT markedly increased radiation-induced DNA damage in cirrhotic liver cancer cells, enhancing their response to radiation. Furthermore, LOX inhibition can be combined with sonoporation to overcome stiffness-related radioresistance, potentially leading to better treatment outcomes for patients with liver cancer.

Conclusions: The findings underscore the significant influence of ECM stiffness on liver cancer's response to radiation. Sonoporation-aided LOX inhibition emerges as a promising strategy to mitigate stiffness-related resistance, offering potential improvements in liver cancer treatment outcomes.

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在三维培养模型中通过剪切波弹性评估 ECM 硬度和肝癌辐射反应。
背景:肿瘤微环境(TME)的硬度直接影响细胞行为。放疗(RT)是实体瘤的常用治疗方法,但肿瘤微环境会影响其疗效。就肝癌而言,临床观察表明,肝硬化、背景较硬的肿瘤对 RT 的反应较小,这表明细胞外基质(ECM)的硬度在放射抗性的形成中起着关键作用:本研究探讨了细胞外基质(ECM)硬度和赖氨酰氧化酶(LOX)同工酶抑制对毫米级三维(3D)培养肝癌放射反应的影响。我们构建了一种基于 ECM 的立方体毫米级水凝胶,其中含有 Huh7 人肝癌细胞。通过调节胶原蛋白浓度,我们制作了两组具有不同 ECM 硬度的样品,以模拟正常肝脏和肝硬化的临床情况。我们使用单传感器系统进行基于剪切波的弹性测量,得出三维细胞培养物的杨氏模量,以研究 ECM 硬度如何影响放射敏感性。这是首次展示在毫米级三维培养物中评估辐射诱导反应的工作流程:结果:ECM 硬度的增加与辐射反应的降低有关。此外,使用 BAPN(β-氨基丙腈单富马酸盐)进行超声辅助抑制 LOX 可显著降低初始 ECM 硬度并增加 RT 诱导的细胞死亡。抑制 LOX 对降低较硬基质中的 ECM 硬度尤其有效。将 LOX 抑制与 RT 结合使用,可明显增加肝硬化肝癌细胞中辐射诱导的 DNA 损伤,增强其对辐射的反应。此外,LOX抑制可与超声修复相结合,克服与僵化相关的放射抗性,从而为肝癌患者带来更好的治疗效果:结论:研究结果强调了ECM僵化对肝癌放射反应的重要影响。声波修复辅助的 LOX 抑制是减轻与僵化相关的抗药性的一种有前途的策略,有可能改善肝癌的治疗效果。
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来源期刊
Radiation Oncology
Radiation Oncology ONCOLOGY-RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
CiteScore
6.50
自引率
2.80%
发文量
181
审稿时长
3-6 weeks
期刊介绍: Radiation Oncology encompasses all aspects of research that impacts on the treatment of cancer using radiation. It publishes findings in molecular and cellular radiation biology, radiation physics, radiation technology, and clinical oncology.
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