Transcriptional regulation of the legumain gene by p53 in HCT116 cells

被引:25
|
作者
Yamane, Takuya [1 ,4 ]
Murao, Sato [1 ]
Kato-Ose, Izumi [1 ]
Kashima, Lisa [1 ,2 ]
Yuguchi, Motoki [3 ]
Kozuka, Miyuki [1 ]
Takeuchi, Keisuke [4 ]
Ogita, Hisakazu [4 ]
Ohkubo, Iwao [5 ]
Ariga, Hiroyoshi [1 ]
机构
[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
[2] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94158 USA
[3] Hokkaido Syst Sci Co Ltd, Div Biosci, Kita Ku, Sapporo, Hokkaido 0010932, Japan
[4] Shiga Univ Med Sci, Dept Biochem & Mol Biol, Div Mol Med Biochem, Otsu, Shiga 5202192, Japan
[5] Tenshi Coll, Sch Nursing & Nutr, Dept Nutr, Higashi Ku, Sapporo, Hokkaido 0650013, Japan
关键词
Legumain; p53; Doxorubicin; ASPARAGINYL ENDOPEPTIDASE; BIOLOGICAL VARIABLES; CYSTATIN E/M; EXPRESSION; CANCER; PROTEIN; MACROPHAGES; DEGRADATION; PROMOTER; CLONING;
D O I
10.1016/j.bbrc.2013.08.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Legumain (EC 3.4.22.34) is an asparaginyl endopeptidase. Strong legumain activity was observed in the mouse kidney, and legumain was found to be highly expressed in tumors. We previously reported that bovine kidney annexin A2 was co-purified with legumain and that legumain cleaved the N-terminal region of annexin A2 at an Asn residue in vitro and in vivo. In this study, we found a p53-binding site in intron 1 of the human legumain gene using computational analysis. To determine whether transcription of the legumain gene is regulated by p53, HCT116 cells were transfected with p53 siRNA and the effect of knockdown of p53 expression on legumain expression was examined. The results showed that expression levels of both legumain mRNA and protein were decreased in the siRNA-treated cells. Furthermore, enzyme activity of legumain was also increased by doxorubicin and its activity was reduced by knockdown of p53 in HCT116 cells. These results suggest that legumain expression and its enzyme activity are regulated by p53. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:613 / 618
页数:6
相关论文
共 50 条
  • [31] Regulation of Tumor Suppressor p53 and HCT116 Cell Physiology by Histone Demethylase JMJD2D/KDM4D
    Kim, Tae-Dong
    Oh, Sangphil
    Shin, Sook
    Janknecht, Ralf
    PLOS ONE, 2012, 7 (04):
  • [32] NAG-1 up-regulation mediated by EGR-1 and p53 is critical for quercetin-induced apoptosis in HCT116 colon carcinoma cells
    Lim, J. H.
    Park, J-W.
    Min, D. S.
    Chang, J-S.
    Lee, Y. H.
    Park, Y. B.
    Choi, K. S.
    Kwon, T. K.
    APOPTOSIS, 2007, 12 (02) : 411 - 421
  • [33] NAG-1 up-regulation mediated by EGR-1 and p53 is critical for quercetin-induced apoptosis in HCT116 colon carcinoma cells
    J. H. Lim
    J.-W. Park
    D. S. Min
    J.-S. Chang
    Y. H. Lee
    Y. B. Park
    K. S. Choi
    T. K. Kwon
    Apoptosis, 2007, 12 : 411 - 421
  • [34] Mechanisms of transcriptional regulation by p53
    Sullivan, Kelly D.
    Galbraith, Matthew D.
    Andrysik, Zdenek
    Espinosa, Joaquin M.
    CELL DEATH AND DIFFERENTIATION, 2018, 25 (01): : 133 - 143
  • [35] Mechanisms of transcriptional regulation by p53
    Kelly D Sullivan
    Matthew D Galbraith
    Zdenek Andrysik
    Joaquin M Espinosa
    Cell Death & Differentiation, 2018, 25 : 133 - 143
  • [36] Regulation of the p53 transcriptional activity
    Liu, G
    Chen, XB
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2006, 97 (03) : 448 - 458
  • [37] Methylsulfonylmethane Induces p53 Independent Apoptosis in HCT-116 Colon Cancer Cells
    Karabay, Arzu Zeynep
    Koc, Asli
    Ozkan, Tulin
    Hekmatshoar, Yalda
    Sunguroglu, Asuman
    Aktan, Fugen
    Buyukbingol, Zeliha
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (07):
  • [38] Transcriptional repression of p53 in immortalized cells transcriptional repression of p53 in immortalized cells
    Kim, HG
    Foster, DN
    MOLECULAR BIOLOGY OF THE CELL, 1998, 9 : 247A - 247A
  • [39] Histone biotinyl transferase activity depends on p53 in HCT 116 colon cancer cells
    Kothapalli, N
    Chew, YC
    Zempleni, J
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2005, 14 (11) : 2687S - 2687S
  • [40] RITA has growth inhibitory activity on colon cancer HCT116 cells expressing wild-type p53, but not SW480 cells harboring mutant p53, via repressing wild-type p53 ubiquitination
    Yu, Xingquan
    Han, Bing
    Guo, Song
    Hu, Baoguang
    Pan, Xiangpo
    Li, Hesheng
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2016, 9 (09): : 17569 - 17578