Jalali Shahrzad, Shi Jie, Ahsan Nagib, Wellik LindaE, Serres MaKayla, Buko Alex, Paludo Jonas, Kim HyoJin, Tang XinYi, Yang Zhi-Zhang, Novak AnneJ, Kyle RobertA, Ansell StephenM
Division of Hematology and Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Division of Hematology and Internal Medicine, Mayo Clinic, Rochester, MN, USA; Department of Hematology, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Redox Biol. 2021 May;41:101927. doi: 10.1016/j.redox.2021.101927. Epub 2021 Mar 4.
The molecular events that modulate the progression of monoclonal gammopathy of undetermined significance of the immunoglobulin M class (IgM-MGUS) to Waldenstrom Macroglobulinemia (WM) are mostly unknown. We implemented comparative proteomics and metabolomics analyses on patient serum samples to identify differentially expressed molecules crucial to the progression from IgM-MGUS to WM. Our data identified altered lipid metabolism as a discriminating factor between MGUS, WM, and matched normal controls. Levels of many fatty acids, including polyunsaturated fatty acids and dicarboxylic acids, were significantly downregulated in WM sera when compared to MGUS. These reductions were associated with diminished 15-LOX and PPAR protein expression and increased 5-LOX and GPX4 expression in WM versus MGUS patients' samples. Furthermore, WM serum samples showed increased lipid peroxidation compared to MGUS. Treatment with IL-6 or TNFα, upstream regulators of differentially expressed proteins between MGUS and WM, increased lipid absorption and lipid peroxidation in WM cell lines. Knock-down of 15-LOX expression increased WM cell survival, an effect accompanied by increased 5-LOX and GPX4 expression. In summary, our data show that reduced fatty acid and lipid metabolite levels in the serum of the WM patients are associated with increased lipid peroxidation and that downregulation of 15-LOX increases the survival of WM cells. These data are highly significant in identifying the biomarkers of disease progression and designing targeted therapeutic intervention.
调节免疫球蛋白M类意义未明的单克隆丙种球蛋白病(IgM-MGUS)进展为华氏巨球蛋白血症(WM)的分子事件大多未知。我们对患者血清样本进行了比较蛋白质组学和代谢组学分析,以鉴定对从IgM-MGUS进展为WM至关重要的差异表达分子。我们的数据确定脂质代谢改变是MGUS、WM与匹配的正常对照之间的鉴别因素。与MGUS相比,WM血清中许多脂肪酸的水平显著下调,包括多不饱和脂肪酸和二羧酸。与MGUS患者样本相比,这些降低与WM中15-脂氧合酶(15-LOX)和过氧化物酶体增殖物激活受体(PPAR)蛋白表达减少以及5-脂氧合酶(5-LOX)和谷胱甘肽过氧化物酶4(GPX4)表达增加有关。此外,与MGUS相比,WM血清样本显示脂质过氧化增加。用MGUS和WM之间差异表达蛋白的上游调节因子白细胞介素-6(IL-6)或肿瘤坏死因子α(TNFα)处理,可增加WM细胞系中的脂质吸收和脂质过氧化。敲低15-LOX表达可增加WM细胞存活,这一效应伴随着5-LOX和GPX4表达增加。总之,我们的数据表明,WM患者血清中脂肪酸和脂质代谢物水平降低与脂质过氧化增加有关,并且15-LOX的下调增加了WM细胞的存活。这些数据对于识别疾病进展的生物标志物和设计靶向治疗干预具有重要意义。