MicroRNAs 143 and 145 are possible common onco-microRNAs in human cancers

被引:43
作者
Akao, Yukihiro
Nakagawa, Yoshihito
Naoe, Tomoki
机构
[1] Gifu Int Inst Biotechnol, Gifu 5040838, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Hematol, Showa Ku, Nagoya, Aichi 4668550, Japan
关键词
microRNAs; 143; and; 145; human cancer; oncomiRNA; ERK5; growth inhibition;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are endogenously expressed RNAs 18-24 nucleotides in length that regulate gene expression through translational repression by binding to a target mRNA. It is thought that the expression level of miRNAs, which act like antioncogenes, is frequently reduced in cancers because of chromosome deletion and epigenetic changes. Since the processing of miRNAs has been characterized to be enzymatic in nature, the expression levels of miRNAs are closely associated with the activity and levels of such enzymes. Here, we found that miRNA 143 and 145 expression levels were extremely reduced in colon cancer cells and commonly in the other kinds of cancer cells tested. The transfection of each precursor miRNA into the cells demonstrated a significant growth inhibition in human colon cancer DLD-1 and SW480 cells, and ERK5 was determined to be the target gene of miRNA 143. Since the presence of genomic loci of the miRNAs was confirmed by PCR in the cell lines and the precursor miRNAs exhibited a growth inhibitory effect in DLD-1 and SW480 cells, the early processes such as transcription and enzymatic modification from primary miRNAs to precursor miRNAs seemed to be commonly disturbed. These findings indicate that the miRNAs 143 and 145 could become good tumor markers and provide an important clue in the study of the mechanism of oncogenesis involving miRNAs.
引用
收藏
页码:845 / 850
页数:6
相关论文
共 19 条
  • [1] MicroRNA functions in animal development and human disease
    Alvarez-Garcia, I
    Miska, EA
    [J]. DEVELOPMENT, 2005, 132 (21): : 4653 - 4662
  • [2] MicroRNA pathways in flies and worms: Growth, death, fat, stress, and timing
    Ambros, V
    [J]. CELL, 2003, 113 (06) : 673 - 676
  • [3] The functions of animal microRNAs
    Ambros, V
    [J]. NATURE, 2004, 431 (7006) : 350 - 355
  • [4] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [5] Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers
    Calin, GA
    Sevignani, C
    Dan Dumitru, C
    Hyslop, T
    Noch, E
    Yendamuri, S
    Shimizu, M
    Rattan, S
    Bullrich, F
    Negrini, M
    Croce, CM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) : 2999 - 3004
  • [6] microRNA-guided posttranscriptional gene regulation
    Chen, PY
    Meister, G
    [J]. BIOLOGICAL CHEMISTRY, 2005, 386 (12) : 1205 - 1218
  • [7] miR-15 and miR-16 induce apoptosis by targeting BCL2
    Cimmino, A
    Calin, GA
    Fabbri, M
    Iorio, MV
    Ferracin, M
    Shimizu, M
    Wojcik, SE
    Aqeilan, RI
    Zupo, S
    Dono, M
    Rassenti, L
    Alder, H
    Volinia, S
    Liu, CG
    Kipps, TJ
    Negrini, M
    Croce, CM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (39) : 13944 - 13949
  • [8] miRNAs, cancer, and stem cell division
    Croce, CM
    Calin, GA
    [J]. CELL, 2005, 122 (01) : 6 - 7
  • [9] Identification of substrates and regulators of mitogen-activated protein kinase ERK5 using chimeric protein kinases
    English, JM
    Pearson, G
    Baer, R
    Cobb, MH
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (07) : 3854 - 3860
  • [10] MicroRNA-143 regulates adipocyte differentiation
    Esau, C
    Kang, XL
    Peralta, E
    Hanson, E
    Marcusson, EG
    Ravichandran, LV
    Sun, YQ
    Koo, S
    Perera, RJ
    Jain, R
    Dean, NM
    Freier, SM
    Bennett, CF
    Lollo, B
    Griffey, R
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (50) : 52361 - 52365