|Table of Contents|

Expression of miR-155 in MALT lymphoma tissues and its relationship with prognosis

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2020 05
Page:
806-809
Research Field:
Publishing date:

Info

Title:
Expression of miR-155 in MALT lymphoma tissues and its relationship with prognosis
Author(s):
Li Li1Yang Yifei2Yang Junchao1Li Weimin1Mao Dan1Shi Xiaoxue1
1.Department of Hematology,Affiliated Hospital of Hebei University of Engineering,Hebei Handan 056000,China;2.Department of Discipline Construction and Graduate Education,Affiliated Hospital(School of Clinical Medicine),Hebei University of Engineering,Hebei Handan 056000,China.
Keywords:
miR-155MALT lymphomaprognosis
PACS:
R733.4
DOI:
10.3969/j.issn.1672-4992.2020.05.026
Abstract:
Objective:To investigate the expression of miR-155 in MALT lymphoma and its relationship with prognosis.Methods:From 2007.03 to 2014.03,a total of 36 patients with MALT lymphoma who were first diagnosed in Department of Hematology of the Affiliated Hospital of Hebei University of Engineering tissues and paraneoplastic tissue (from tumor >2 cm) were collected.Using qPCR methods to detect the expression of miR-155 in tumor tissues and paraneoplastic tissues of patients with MALT lymphoma,then 36 patients were given CHOP regimen treatment for 8 cycles.According to the evaluation criteria of solid tumor efficacy,the patients were divided into active group and inactive group.Serum levels of miR-155 in two groups of patients were compared,and patients were followed-up by clinic or by phone.According to the threshold of the average value of miR-155 expression level,the patients were divided into miR-155 high expression group (23 patients)and miR-155 low expression group (13 patients).The three-year survival rate of the two groups of patients was compared.Results:The expression levels of miR-155 in tumor tissues and paraneoplastic tissues respectively were 6.63±0.70 and 1.29±0.05,and the differences was statistically significant(P<0.05).After 8 cycles of CHOP treatment,the serum levels of miR-155 in the effective and ineffective groups respectively were 2.21±0.14 and 7.01±0.54.The follow-up showed that after treatment the three-year survival rates of patients with miR-155 high expression group and miR-155 low expression group respectively were 56.5% and 76.9%,and the differences was statistically significant(P<0.05).Conclusion:The expression level of miR-155 may be related to the development and prognosis of MALT lymphoma.

References:

[1]Shimizu K,Yoshida J,Kakegawa S,et al.Primary thymicmucosa-associated lymphoid tissue lymphoma:Diagnostic tips[J].J Thorac Oncol,2010,5(1):117-121.
[2]Bonnet C,Fillet G,Mounier N,et al.CHOP alone compared with CHOP plus radiotherapy for localized aggressive lymphoma in elderly patients:A study by the Groupe d' Etude des Lymphomes de l'Adulte[J].J Clin Oncol,2007,25(7):787-792.
[3]Lemer C,Wemmert S,Bochen F,et al.Characterization of miR-146a and miR-155 in blood,tissue and cell lines of head and neck squamous cell carcinoma patients and their impact on cell proliferation and migration[J].J Cancer Res Clin Oncol,2016,142(4):757-766.
[4]Lutherborrow M,Bryant A,Jayaswal V,et al.Expression profiling of cytogenetically nornal acute myeloid leukemia identifies microRNAs that target genes involved in monocytic differentiation[J].Am J Hematol,2011,86(1):2-11.
[5]LUO ZM,ZHOU D,ZHOU XF,et al.Expression of miRNA-155 in acute myeloid leukemia and its clinical significance[J].Modern Oncology,2019,27(02):316-318.[罗自勉,周丹,周新伏,等.miRNA-155在急性髓系白血病不同阶段中的表达及临床意义[J].现代肿瘤医学,2019,27(02):316-318.]
[6]Zhu M,Wang M,Yang F,et al.miR-155-5p inhibtion promotes the transition of bone marrow mesenchymal stem cells to gastric cancer tissue derived MSC-like cells via NF-κB p65 activation[J].Oncotarget,2016,7(13):16567-16580.
[7]LI L,YANG YF,YANG JC,et al.The expression and clinical significance of miR-155 and miR-21 in extranodal zone lymphoma of mucosa associated lymphoid tissue[J].J Clinl Hematol,2018,31(3):201-204.[李丽,杨一飞,杨俊超,等.miR-155、miR-21在黏膜相关淋巴样组织结外边缘区淋巴瘤组织和细胞中的表达及意义[J].临床血液学杂志,2018,31(3):201-204.]
[8]Therasse P,Arbuck SG,Eisenhauer EA,et al.New guidelines to evaluate the response to treatment in solid tumors.European organization for research and treatment of cancer,national cancer institute of the united states,national cancer institute of canada[J].J Natl Cancer Inst,2000,92(3):205-216.
[9]Bartel DP.MicroRNAs:Genomics,biogenesis,mechanism,and function[J].Cell,2004,116(2):281-297.
[10]Adlakha YK,Saini N.Brain microRNAs and insights into biological functions and therapeutic potential of brain enriched miRNA-128[J].Mol Cancer,2014,13(02):33.
[11]Roccaro AM,Sacco A,Husu EN,et al.Dual targeting of the PI3K/Akt/mTOR pathway as an antitumor strategy in Waldenstorm macroglobulinemia[J].Blood,2010,115(3):559-569.
[12]Liu Z,Smith KR,Khong HT,et al.MiR-125b regulates differentiation and metabolic reprogramming of T cell acute lymphoblastic leukemia by directly targeting A20[J].Oncotarget,2016,7(48):78667-78679.
[13]Schotte D,De Menezes RX,Akbari Moqadam F,et al.MicroRNA characterize genetic diversity and drug resistance in pediatric acute lymphoblastic leukemia[J].Haematologica,2011,9(5):703-711.
[14]Meng F,Henson R,Wehbe-Janek H,et al.MicroRNA-21 regulates expression of the PTEN tumor suppressor gene in human hepatocellular cancer[J].Gastroenterology,2007,133(2):647-658.
[15]Lawrie C,Soneji S,Marafioti T,et al.MicroRNA expression distinguishes between germinal center B cell-like and activated B cell like subtypes of diffuse large B cell lymphoma[J].Int J Cancer,2007,121(5):1156-1161.

Memo

Memo:
河北省重点研发计划健康医疗与生物医药专项项目(编号:18277782D);邯郸市科学技术研究与发展计划项目(编号:1723208068-2)
Last Update: 1900-01-01