Fajardo-Ramirez Oscar Raul, Villela Luis, Campa-Carranza Jocelyn Nikita, Perez-Maya Antonio Ali, Borrego-Soto Gissela, Wah-Suarez Martin Ivan, Rodríguez-Sánchez Iram Pablo, Zapata-Morin Patricio A, Ortiz-Lopez Rocio, Treviño Victor Manuel, Garcia-Magariño Mariano, Marino-Martinez Ivan Alberto
Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud de la Salud, Mexico.
Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado de Sonora (ISSSTESON), Centro Médico Dr. Ignacio Chavez, Mexico.
Noncoding RNA Res. 2020 Oct 10;5(4):185-190. doi: 10.1016/j.ncrna.2020.10.001. eCollection 2020 Dec.
Refractoriness remains as one of the challenges in patients with lymphoma under chemotherapy, and among biological regulators in cells driving this type of response are microRNAs (miRNAs). Different genes are constantly turned on or off according to the miRNAs expression profiles affecting the drug response in patients and their stability in serum and plasma makes them potential prognostic biomarkers in several diseases. Here we described a profile of miRNAs in plasma of diffuse large B cell lymphoma (DLBCL) patients. miRNA expression arrays were carried using pre-treatment plasma samples of sixteen patients, followed by a comparison between the responder and the non-responders. After six cycles of R-CHOP treatment, twelve out of sixteen patients were clinically diagnosed with complete response while in four patients no clinical response was observed. Between these groups, a signature of fifteen differential expressed miRNAs was found. The circulating miRNAs in plasma of patients with no response were related to the drug resistance in other types of cancer, by targeting genes involved in cell proliferation and apoptosis, among other cell processes.
难治性仍然是淋巴瘤患者化疗面临的挑战之一,而在驱动这种反应的细胞生物学调节因子中,微小RNA(miRNA)是其中之一。根据miRNA表达谱,不同基因不断开启或关闭,这影响患者的药物反应,并且它们在血清和血浆中的稳定性使其成为多种疾病中潜在的预后生物标志物。在此,我们描述了弥漫性大B细胞淋巴瘤(DLBCL)患者血浆中的miRNA谱。使用16例患者的治疗前血浆样本进行miRNA表达阵列分析,随后比较反应者和无反应者。经过6个周期的R-CHOP治疗后,16例患者中有12例临床诊断为完全缓解,而4例患者未观察到临床反应。在这些组之间,发现了15种差异表达miRNA的特征。无反应患者血浆中的循环miRNA通过靶向参与细胞增殖和凋亡等其他细胞过程的基因,与其他类型癌症的耐药性有关。