血清miR-124-3p表达升高与直肠癌患者新辅助放化疗后的高生存率相关

S. N. Wahyuningrum, C. H. N. Priharsanti, S. Haryana, A. Ghozali
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摘要

背景:结直肠癌是世界上发病率第三高的癌症,其中30%的病例为直肠癌。目前,还没有找到有效的诊断指标来准确预测患者对治疗的反应。一些研究表明,miRNA有作为预后生物标志物的潜力。MiR-1243p作为肿瘤抑制因子,在部分肿瘤中显著下调,对人结直肠癌细胞具有放射致敏作用。本研究旨在探讨直肠癌患者接受nCRT后miR-124-3p的表达情况,并分析其与患者生存及其他临床参数的关系。方法:本研究纳入组织学证实的局部晚期直肠癌(LARC)患者15例,接受新辅助化疗/nCRT(放疗45-50 Gy, 1,8-2 Gy, 1 ~ 3个月,化疗5-氟尿嘧啶口服)。新辅助放化疗前后取患者外周静脉血(5ml)。采用qRT-PCR检测miR-124-3p的表达,采用Livak法计算。结果:在本研究中,我们发现miR-124的升高与直肠癌患者的高生存率显著相关(P = 0.003;Or =30, 95% ci = 1,41 - 638,15)。nCRT后miR-124-3p平均表达量显著升高(P< 0.041,前变化倍数=1,14±1,25;后=2,4±1,84)。结论:我们的发现表明,miR-124-3p在血清中的表达有可能作为预测直肠癌患者新辅助放化疗后生存的生物标志物。(印尼卫生科学杂志2019;10(2):90-5)
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Increasing serum miR-124-3p expression is associated with the high survival rate of a rectal cancer patient after neoadjuvant chemoradiotherapy
Background: Colorectal cancer is the world’s third most prevalent cancer, which 30% of cases are rectal cancer. Today, the effective diagnostic marker to accurately predict clinical outcome patients response to therapy did not found yet. Several research studies have indicated that miRNA potential as a prognostic biomarker. MiR-1243p plays as tumor suppressor that significantly down-regulated in some cancer and could radiosensitize human colorectal cancer cells. The aim of the study is to investigate the expression of miR-124-3p from rectal cancer patient who receive nCRT, and analyze its association with patient survival and others clinical parameters. Methods: This research involved 15 patients with histologically confirmed locally advanced rectal cancer (LARC) and received neoadjuvant chemotherapy/nCRT (radiotherapy 45-50 Gy with 1,8-2 Gy fractions over 1 to 3 months and chemotherapy 5-fluorouracil was administered orally). Patient blood (5 ml) were collected from peripheral venous before and after neoadjuvant chemoradiotherapy. miR-124-3p expression was performed using qRT-PCR and calculate using Livak method. Results: In this study, we found that increasing of miR-124 was significantly associate with high survival of rectal cancer patient (P = 0,003; OR =30, 95% CI = 1,41 – 638,15). Average of miR-124-3p expression increase significantly after nCRT (P<0,041, fold change before=1,14 ± 1,25; after=2,4 ± 1,84). Conclusion: Our finding suggests that miR-124-3p expression in blood serum was potential as biomarkers to predict rectal cancer patient survival after neoajduvant chemoradiotherapy. (Health Science Journal of Indonesia 2019;10(2):90-5)
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