NHC and CAMS Key Laboratory of Molecular Probe and Targeted Theranostics, Harbin Medical University, Harbin, China.
Molecular Imaging Research Center (MIRC), Harbin Medical University, Harbin, China.
J Magn Reson Imaging. 2021 Apr;53(4):995-1014. doi: 10.1002/jmri.27147. Epub 2020 Mar 26.
The influx of sodium (Na ) ions into a resting cell is regulated by Na channels and by Na /H and Na /Ca exchangers, whereas Na ion efflux is mediated by the activity of Na /K -ATPase to maintain a high transmembrane Na ion gradient. Dysfunction of this system leads to changes in the intracellular sodium concentration that promotes cancer metastasis by mediating invasion and migration. In addition, the accumulation of extracellular Na ions in cancer due to inflammation contributes to tumor immunogenicity. Thus, alterations in the Na ion concentration may potentially be used as a biomarker for malignant tumor diagnosis and prognosis. However, current limitations in detection technology and a complex tumor microenvironment present significant challenges for the in vivo assessment of Na concentration in tumor. Na-magnetic resonance imaging ( Na-MRI) offers a unique opportunity to study the effects of Na ion concentration changes in cancer. Although challenged by a low signal-to-noise ratio, the development of ultrahigh magnetic field scanners and specialized sodium acquisition sequences has significantly advanced Na-MRI. Na-MRI provides biochemical information that reflects cell viability, structural integrity, and energy metabolism, and has been shown to reveal rapid treatment response at the molecular level before morphological changes occur. Here we review the basis of Na-MRI technology and discuss its potential as a direct noninvasive in vivo diagnostic and prognostic biomarker for cancer therapy, particularly in cancer immunotherapy. We propose that Na-MRI is a promising method with a wide range of applications in the tumor immuno-microenvironment research field and in cancer immunotherapy monitoring. LEVEL OF EVIDENCE: 2 TECHNICAL EFFICACY: Stage 2.
钠离子(Na+)流入静息细胞受 Na 通道和 Na+/H+和 Na+/Ca2+交换器调节,而 Na+离子外排则由 Na+/K+-ATP 酶的活性介导,以维持高跨膜 Na+离子梯度。该系统的功能障碍导致细胞内钠离子浓度发生变化,通过介导侵袭和迁移促进癌症转移。此外,由于炎症导致的细胞外 Na+离子在癌症中的积累有助于肿瘤免疫原性。因此,Na 离子浓度的改变可能潜在地用作恶性肿瘤诊断和预后的生物标志物。然而,目前检测技术的局限性和复杂的肿瘤微环境对肿瘤内 Na 浓度的体内评估提出了重大挑战。Na 磁共振成像(Na-MRI)为研究癌症中 Na 离子浓度变化的影响提供了独特的机会。尽管受到低信噪比的挑战,但超高磁场扫描仪和专门的钠采集序列的发展极大地推进了 Na-MRI。Na-MRI 提供了反映细胞活力、结构完整性和能量代谢的生化信息,并已显示出在形态学变化发生之前在分子水平上揭示快速治疗反应的能力。在这里,我们回顾了 Na-MRI 技术的基础,并讨论了其作为癌症治疗的直接无创体内诊断和预后生物标志物的潜力,特别是在癌症免疫治疗中。我们提出,Na-MRI 是一种很有前途的方法,在肿瘤免疫微环境研究领域和癌症免疫治疗监测中有广泛的应用。证据水平:2 技术功效:阶段 2。