Donzelli Sara, Farneti Alessia, Marucci Laura, Ganci Federica, Sacconi Andrea, Strano Sabrina, Sanguineti Giuseppe, Blandino Giovanni
Oncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Radiotherapy Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Front Cell Dev Biol. 2020 Apr 21;8:257. doi: 10.3389/fcell.2020.00257. eCollection 2020.
Cachexia is a complex metabolic syndrome that determines a severe body weight loss characterized by a marked reduction in muscle mass. About 80% of patients with advanced cancer develop cachexia due to both the tumor itself and cancer treatment (radiotherapy and/or chemotherapy), which is associated to a worse prognosis. Despite its clinical relevance, this syndrome is still under-diagnosed and it lacks effective treatments. Radio-chemotherapy treatment is essential in patients with advanced head and neck cancers (HNSCC). Although this treatment has improved patients' life expectancy, it has also dramatically increased their need for assistance and support. The management of adverse symptoms, including cachexia, is of great importance in order to avoid delays in therapy, reduction of dosages and hospitalizations. MicroRNAs (miRNAs) are small non-coding RNA molecules, which have emerged as powerful biomarkers in stratifying human cancers. Due to their high stability in body fluids, miRNAs might be excellent non-invasive biomarkers for the early detection and follow-up of cancer patients. Here, we will summarize the current knowledge and debate the strong need to identify circulating biomarkers for the early diagnosis of cachexia. We will propose circulating non-coding RNAs as biomarkers for detecting early cachexia and implementing specific treatment. We will also discuss the potential use of circulating miRNAs as biomarkers of cachexia in HNSCC patients' blood samples collected before and after radio-chemotherapy treatment. Our intent is to pave the way to the identification of specific circulating miRNAs associated to cachexia occurrence and to the design of specific interventions aimed at improving the quality of life of cancer patients.
恶病质是一种复杂的代谢综合征,其特征为严重体重减轻,伴有肌肉量显著减少。约80%的晚期癌症患者会因肿瘤本身以及癌症治疗(放疗和/或化疗)而发生恶病质,这与更差的预后相关。尽管该综合征具有临床相关性,但仍诊断不足且缺乏有效治疗方法。放化疗对晚期头颈癌(HNSCC)患者至关重要。虽然这种治疗提高了患者的预期寿命,但也大幅增加了他们对援助和支持的需求。为避免治疗延误、剂量减少和住院,对包括恶病质在内的不良症状进行管理非常重要。微小RNA(miRNA)是小的非编码RNA分子,已成为人类癌症分层中的强大生物标志物。由于其在体液中的高稳定性,miRNA可能是癌症患者早期检测和随访的优秀非侵入性生物标志物。在此,我们将总结当前的知识,并探讨识别恶病质早期诊断循环生物标志物的迫切需求。我们将提出循环非编码RNA作为检测早期恶病质和实施特定治疗的生物标志物。我们还将讨论循环miRNA作为HNSCC患者放化疗前后采集的血样中恶病质生物标志物的潜在用途。我们的目的是为识别与恶病质发生相关的特定循环miRNA以及设计旨在改善癌症患者生活质量的特定干预措施铺平道路。