Goto Taichi, Saligan Leorey N
Symptoms Biology Unit, National Institute of Nursing Research, National Institutes of Health, Bethesda, Maryland, USA.
Curr Opin Support Palliat Care. 2024 Sep 1;18(3):161-167. doi: 10.1097/SPC.0000000000000706. Epub 2024 May 27.
This focused, narrative review mostly describes our team's investigations into the potential inflammatory mechanisms that contribute to the development of cancer-related gastrointestinal (GI) mucositis and its associated symptoms. This review summarizes details of our clinical and preclinical findings to test the role of inflammation in the development and occurrence of these cancer-related conditions.
GI mucositis (GIM) is a common, distressing condition reported by cancer patients. GIM is often clustered with other behaviors including fatigue, pain, anorexia, depression, and diarrhea. It is hypothesized that there is a common biologic mechanism underpinning this symptom cluster. Our multi-platform investigations revealed that GIM and its associated cluster of behaviors may be triggered by local inflammation spreading systemically causing pro-inflammatory-mediated toxicities, leading to alterations in immune, metabolic, and nervous system functions and activities. For example, behavioral toxicities related to local irradiation for non-metastatic cancer may be triggered by mGluR5 activation influencing prolonged T cell as well as NF-κB transcription factor activities. Thus, interventions targeting inflammation and associated pathways may be a reasonable strategy to alleviate GIM and its symptom cluster.
GIM may be a sign of a broader systemic inflammatory response triggered by cancer or its treatment. Addressing GIM and its associated symptoms primarily involves supportive care strategies focused on relieving symptoms, promoting healing, and preventing complications.
本篇重点叙述性综述主要描述了我们团队对可能导致癌症相关胃肠道(GI)黏膜炎及其相关症状发展的潜在炎症机制的研究。本综述总结了我们临床和临床前研究结果的细节,以检验炎症在这些癌症相关病症发生和发展中的作用。
胃肠道黏膜炎(GIM)是癌症患者报告的一种常见且令人痛苦的病症。GIM常与其他症状同时出现,包括疲劳、疼痛、厌食、抑郁和腹泻。据推测,存在一种共同的生物学机制支撑着这一症状群。我们的多平台研究表明,GIM及其相关症状群可能是由局部炎症全身性扩散引发促炎介导的毒性作用所致,进而导致免疫、代谢和神经系统功能及活动发生改变。例如,非转移性癌症局部放疗相关的行为毒性可能是由代谢型谷氨酸受体5(mGluR5)激活影响延长的T细胞以及核因子κB(NF-κB)转录因子活性所触发。因此,针对炎症及相关途径的干预措施可能是缓解GIM及其症状群的合理策略。
GIM可能是癌症或其治疗引发的更广泛全身炎症反应的一个迹象。应对GIM及其相关症状主要涉及以缓解症状、促进愈合和预防并发症为重点的支持性护理策略。