Department of Radiology and Research Institute of Radiological Science, Yonsei University College of Medicine, Seoul, South Korea.
Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
NMR Biomed. 2021 Aug;34(8):e4561. doi: 10.1002/nbm.4561. Epub 2021 Jun 3.
An increase in hyperpolarized (HP) [1- C]lactate production has been suggested as a biomarker for cancer occurrence as well as for response monitoring of cancer treatment. Recently, the use of metformin has been suggested as an anticancer or adjuvant treatment. By regulating the cytosolic NAD /NADH redox state, metformin stimulates lactate production and increases the HP [1- C]lactate conversion rate in the kidney, liver, and heart. In general, increased HP [1- C]lactate is regarded as a sign of cancer occurrence or tumor growth. Thus, the relationship between the tumor suppression effect of metformin and the change in metabolism monitored by HP [1- C]pyruvate MRS in cancer treatment needs to be investigated. The present study was performed using a brain metastasis animal model with MDA-MB-231(BR)-Luc breast cancer cells. HP [1- C]pyruvate MRS, T -weighted MRI, and bioluminescence imaging were performed in groups treated with metformin or adjuvant metformin and radiation therapy. Metformin treatment alone did not display a tumor suppression effect, and the HP [1- C]lactate conversion rate increased. In radiation therapy, the HP [1- C]lactate conversion rate decreased with tumor suppression, with a p-value of 0.028. In the adjuvant metformin and radiation treatment, the tumor suppression effect increased, with a p-value of 0.001. However, the apparent HP [1- C]lactate conversion rate (K ) was observed to be offset by two opposite effects: a decrease on radiation therapy and an increase caused by metformin treatment. Although HP [1- C]pyruvate MRS could not evaluate the tumor suppression effect of adjuvant metformin and radiation therapy due to the offset phenomenon, metabolic changes following only metformin pre-treatment could be monitored. Therefore, our results indicate that the interpretation of HP [1- C]pyruvate MRS for response monitoring of cancer treatment should be carried out with caution when metformin is used as an adjuvant cancer therapy.
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高极化（HP）[1-13C]乳酸生成的增加被认为是癌症发生的生物标志物，以及癌症治疗反应监测的生物标志物。最近，已经提出使用二甲双胍作为抗癌或辅助治疗。通过调节细胞溶质 NAD/NADH 氧化还原状态，二甲双胍刺激乳酸生成，并增加肾脏、肝脏和心脏中的 HP[1-13C]乳酸转化率。一般来说，增加的 HP[1-13C]乳酸被认为是癌症发生或肿瘤生长的标志。因此，需要研究二甲双胍的肿瘤抑制作用与癌症治疗中 HP[1-13C]丙酮酸 MRS 监测的代谢变化之间的关系。本研究使用 MDA-MB-231（BR）-Luc 乳腺癌细胞的脑转移动物模型进行。在接受二甲双胍或辅助二甲双胍和放射治疗的组中进行 HP[1-13C]丙酮酸 MRS、T1 加权 MRI 和生物发光成像。单独使用二甲双胍治疗没有显示出肿瘤抑制作用，并且 HP[1-13C]乳酸转化率增加。在放射治疗中，HP[1-13C]乳酸转化率随着肿瘤抑制而降低，p 值为 0.028。在辅助二甲双胍和放射治疗中，肿瘤抑制作用增加，p 值为 0.001。然而，观察到 HP[1-13C]丙酮酸 MRS 的表观（1-13C]乳酸转化率（K）被两种相反的效应抵消：放射治疗降低和二甲双胍治疗增加。尽管由于抵消现象，HP[1-13C]丙酮酸 MRS 无法评估辅助二甲双胍和放射治疗的肿瘤抑制作用，但可以监测仅二甲双胍预处理后的代谢变化。因此，我们的结果表明，在使用二甲双胍作为辅助癌症治疗时，应谨慎解释 HP[1-13C]丙酮酸 MRS 以监测癌症治疗的反应。
