Maaroufi Aria, Khadem-Ansari Mohammad-Hasan, Khalkhali Hamid-Reza, Rasmi Yousef
Department of Biochemistry, Urmia University of Medical Sciences, Urmia, Iran.
Department of Biostatistics, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
J Cancer Res Ther. 2020 Jan-Mar;16(1):98-101. doi: 10.4103/jcrt.JCRT_666_16.
The fluctuations of proteins in multiple myeloma (MM) are well-known markers for checking the status of the patients.
The objective of this study was to examine three proteins that have an important role in disease progression.
The study was performed with two groups: 30 MM stage I patients' (14 females/16 males; aged 60.83 ± 12.38 years) as case group and 40 healthy individuals (18 females/22 males; aged 57.65 ± 6.43 years) as control group. Both groups have been matched in gender and age. Bone sialoprotein (BSP), osteopontin (OPN), and β2-microglobulin (β2M) were measured with an enzyme-linked immunosorbent assay.
Serum BSP levels of MM-I patients was significantly higher than that of healthy controls (29.24 ± 5.57 vs. 20.89 ± 3.67, P = 0.001). OPN levels of MM-I patients were significantly lower than that of healthy individuals (12.03 ± 3.45 vs. 19.35 ± 4.67, P = 0.001). β2M levels of patients and controls were similar (1.49 ± 0.67 vs. 1.29 ± 0.55, P = 0.193).
The results suggested that myeloma cells may affect the production of BSP and OPN, which possibly contributes to osteoclastic bone resorption in MM-I patients. Their levels may be a useful biomarker for assessing bone destruction in MM-I patients and distinguishing MM-I from healthy individuals.
多发性骨髓瘤(MM)中蛋白质的波动是检查患者病情的知名标志物。
本研究的目的是检测三种在疾病进展中起重要作用的蛋白质。
本研究分为两组进行:30例I期MM患者(14例女性/16例男性;年龄60.83±12.38岁)作为病例组,40例健康个体(18例女性/22例男性;年龄57.65±6.43岁)作为对照组。两组在性别和年龄上进行了匹配。采用酶联免疫吸附测定法检测骨唾液蛋白(BSP)、骨桥蛋白(OPN)和β2微球蛋白(β2M)。
MM-I患者的血清BSP水平显著高于健康对照组(29.24±5.57 vs.20.89±3.67,P = 0.001)。MM-I患者的OPN水平显著低于健康个体(12.03±3.45 vs.19.35±4.67,P = 0.001)。患者和对照组的β2M水平相似(1.49±0.67 vs.1.29±0.55,P = 0.193)。
结果表明,骨髓瘤细胞可能影响BSP和OPN的产生,这可能导致MM-I患者的破骨细胞骨吸收。它们的水平可能是评估MM-I患者骨破坏以及区分MM-I患者与健康个体的有用生物标志物。