Literature DB >> 28058629

RNAi-mediated knockdown of MCM7 gene on CML cells and its therapeutic potential for leukemia.

Liang Tian1, Juan Liu2, Guo-Hua Xia3, Bao-An Chen4.   

Abstract

MCM7 is one of the subunits of MCM2-7 complex, which is essential to DNA replication licensing and the control of cell cycle progression. It has been demonstrated that MCM7 participates in mRNA transcription and DNA damage regulation as well. MCM7 gene is found to be over-expressed in multiple cancers, but there are few reports about its effect in leukemia. Recent studies have proven that MCM7 expression has a relationship with diagnosis and prognosis, which has led to their potential clinical application as a marker for cancer screening. RNA interference (RNAi) is a biological process in which RNA molecules inhibit gene expression, typically by causing the destruction of specific mRNA molecules. It is a valuable research tool, which is widely used in cell culture and living organisms as well as in medicine recent years. It is indicated that RNAi application for targeting functional carcinogenic molecules, tumor resistance to chemotherapy and radiotherapy is required in cancer treatment. Gene products knockdown by RNAi technology exerts anti-proliferative and pro-apoptotic effects upon cell culture systems, animal models and in clinical trials in the most studies. In the present study, we found that MCM7 highly expressed in K562 cells rather than that in normal neutrophils. Thus, lentivirus-mediated shRNA targeting MCM7 was used to suppress its endogenous expression in K562 cells and develop a novel therapeutic strategy for leukemia.

Entities:  

Keywords:  K562 cell; Lentivirus-mediated siRNA; Leukemia; MCM7 gene

Mesh:

Substances:

Year:  2017        PMID: 28058629     DOI: 10.1007/s12032-016-0878-x

Source DB:  PubMed          Journal:  Med Oncol        ISSN: 1357-0560            Impact factor:   3.064


  50 in total

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Authors:  B K Tye
Journal:  Annu Rev Biochem       Date:  1999       Impact factor: 23.643

2.  A lethal dose of RNA.

Authors:  Kai Kupferschmidt
Journal:  Science       Date:  2013-08-16       Impact factor: 47.728

Review 3.  The role of MCM/P1 proteins in the licensing of DNA replication.

Authors:  J P Chong; P Thömmes; J J Blow
Journal:  Trends Biochem Sci       Date:  1996-03       Impact factor: 13.807

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Authors:  Weiqi Tan; Yang Li; Seng-Gee Lim; Theresa M C Tan
Journal:  World J Gastroenterol       Date:  2014-05-28       Impact factor: 5.742

Review 5.  Plk1-targeted small molecule inhibitors: molecular basis for their potency and specificity.

Authors:  Ravichandran N Murugan; Jung-Eun Park; Eun-Hee Kim; Song Yub Shin; Chaejoon Cheong; Kyung S Lee; Jeong Kyu Bang
Journal:  Mol Cells       Date:  2011-07-29       Impact factor: 5.034

6.  Roles of Mcm7 and Mcm4 subunits in the DNA helicase activity of the mouse Mcm4/6/7 complex.

Authors:  Zhiying You; Yukio Ishimi; Hisao Masai; Fumio Hanaoka
Journal:  J Biol Chem       Date:  2002-08-30       Impact factor: 5.157

7.  Histone deacetylase inhibitor SAHA epigenetically regulates miR-17-92 cluster and MCM7 to upregulate MICA expression in hepatoma.

Authors:  H Yang; P Lan; Z Hou; Y Guan; J Zhang; W Xu; Z Tian; C Zhang
Journal:  Br J Cancer       Date:  2014-11-13       Impact factor: 7.640

Review 8.  MCM Paradox: Abundance of Eukaryotic Replicative Helicases and Genomic Integrity.

Authors:  Mitali Das; Sunita Singh; Satyajit Pradhan; Gopeshwar Narayan
Journal:  Mol Biol Int       Date:  2014-10-19

Review 9.  Bioactive lipids and the control of Bax pro-apoptotic activity.

Authors:  V Mignard; L Lalier; F Paris; F M Vallette
Journal:  Cell Death Dis       Date:  2014-05-29       Impact factor: 8.469

Review 10.  Polo-like kinase-1 in DNA damage response.

Authors:  Sun-Yi Hyun; Hyo-In Hwang; Hyo-In Hwan; Young-Joo Jang
Journal:  BMB Rep       Date:  2014-05       Impact factor: 4.778

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2.  Transcription factor binding site clusters identify target genes with similar tissue-wide expression and buffer against mutations.

Authors:  Ruipeng Lu; Peter K Rogan
Journal:  F1000Res       Date:  2018-12-14

3.  Modelling the Effects of MCM7 Variants, Somatic Mutations, and Clinical Features on Acute Myeloid Leukemia Susceptibility and Prognosis.

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4.  Clarifying the molecular mechanism of tomentosin‑induced antiproliferative and proapoptotic effects in human multiple myeloma via gene expression profile and genetic interaction network analysis.

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Journal:  Int J Mol Med       Date:  2021-10-13       Impact factor: 4.101

5.  MINA53 deficiency leads to glioblastoma cell apoptosis via inducing DNA replication stress and diminishing DNA damage response.

Authors:  Fan Xuan; Mengying Huang; Erhu Zhao; Hongjuan Cui
Journal:  Cell Death Dis       Date:  2018-10-17       Impact factor: 8.469

Review 6.  Viral Vector-Based Melanoma Gene Therapy.

Authors:  Altijana Hromic-Jahjefendic; Kenneth Lundstrom
Journal:  Biomedicines       Date:  2020-03-16
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