microRNAs作为肝癌免疫治疗的预测因子

Rui Han
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摘要

肝细胞癌(HCC)是最常见的肝癌类型。不幸的是,它经常在晚期被诊断出来,限制了可用的治疗选择。免疫检查点抑制剂(ICIs)已显示出治疗HCC的希望,尽管其有效性因患者而异,并可能导致不良副作用。为了提高治疗效果并确保患者安全,有必要对副作用进行密切监测和早期干预。因此,选择能够预测HCC对ICIs反应的生物标志物变得至关重要。microrna在调节HCC基因表达中起着至关重要的作用,已成为预测治疗反应的潜在生物标志物。已经发现一些microrna会影响ICIs,如CTLA-4和PD-L1,它们是检查点抑制剂治疗的靶点。通过识别可以预测对ICIs反应的特定microrna,医疗保健提供者可以为HCC患者制定个性化的治疗计划。这种量身定制的方法优化了资源利用,并将不良副作用的风险降至最低。最终,这种个性化策略可以改善HCC患者的治疗效果并提高其生活质量。因此,选择能够预测HCC治疗中ICIs反应的microrna具有重要意义。它有可能提高患者的反应率,减少不良反应,并优化医疗资源的利用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
microRNAs act as a predictor in liver cancer immunotherapy
Hepatocellular carcinoma (HCC) is the most common type of liver cancer. Unfortunately, it is frequently diagnosed in advanced stages, limiting the available treatment options. Immune checkpoint inhibitors (ICIs) have shown promise in treating HCC, although their effectiveness varies among patients and can result in undesirable side effects. To enhance treatment outcomes and ensure patient safety, close monitoring and early intervention for side effects are necessary. Consequently, the selection of biomarkers that can predict the response to ICIs in HCC becomes crucial. MicroRNAs, which play a vital role in regulating gene expression in HCC, have emerged as potential biomarkers for predicting treatment response. Some microRNAs have been found to affect ICIs such as CTLA-4 and PD-L1, which are the targets of checkpoint inhibitor therapy. By identifying specific microRNAs that can forecast the response to ICIs, healthcare providers can personalize treatment plans for HCC patients. This tailored approach optimizes resource utilization and minimizes the risk of adverse side effects. Ultimately, this personalized strategy can improve treatment outcomes and enhance the quality of life for individuals with HCC. Thus, the selection of microRNAs capable of predicting the response to ICIs in HCC treatment holds significant importance. It has the potential to enhance patient response rates, decrease adverse effects, and optimize the utilization of healthcare resources.
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