Expression of p53β and Δ133p53 isoforms in different gastric tissues

被引:1
|
作者
Ji, Wansheng [1 ]
Zhang, Na [2 ]
Zhang, Hongmei [1 ]
Ma, Jingrong [2 ]
Zhong, Hua [1 ]
Jiao, Jianxin [1 ]
Gao, Zhixing [1 ]
机构
[1] Weifang Med Univ, Affiliated Hosp, Dept Gastroenterol, Weifang 261031, Peoples R China
[2] Weifang Med Univ, Grad Sch, Weifang 261042, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2015年 / 8卷 / 09期
关键词
Gastric carcinoma; p53; beta; Delta; 133p53; isoforms; ACUTE MYELOID-LEUKEMIA; SEROUS OVARIAN-CANCER; P53; ISOFORMS; TUMOR-SUPPRESSOR; TRANSCRIPTIONAL ACTIVITY; MUTATION STATUS; CELL CARCINOMA; BREAST-CANCER; DELTA-40P53; DELTA-P53;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study aims to detect the mRNA of p53 beta and Delta 133p53 isoforms in three gastric carcinoma cell lines and tissues of superficial gastritis, atrophic gastritis, gastric carcinoma, or paracancerous area. Nested reverse transcription PCR was used to detect the mRNA of p53 beta and Delta 133p53 isoforms in tissues of superficial gastritis, chronic atrophic gastritis, gastric cancer cell lines (SGC-7901, MKN45, KATO III), gastric adenocarcinoma, and paracancerous lesion. The amplified products were shown by agarose gel electrophoresis. The expression difference among various tissues was analyzed by x(2) tests. The positive rates of Delta 133p53 mRNA were 73.3% (11/15) in gastric adenocarcinoma and 20% (3/15) in paracancerous tissue, whereas the positive rates of p53 beta mRNA were 20% (3/15) in gastric adenocarcinoma and 66.7% (10/15) in paracancerous tissue. The difference between adenocarcinoma and paracancerous tissues was significant (P<0.05). The positive rates of Delta 133p53 mRNA were 25% (5/20), 50% (15/30), and 75% (15/20), respectively, in superficial gastritis, atrophic gastritis, and gastric adenocarcinoma; the positive rates of p53 beta mRNA were 65% (13/20), 33.3% (10/30), and 25% (5/20), respectively, in superficial gastritis, atrophic gastritis, and gastric adenocarcinoma. The difference between adenocarcinoma and superficial gastritis samples was significant (P<0.05). Both p53 beta and Delta 133p53 mRNAs were positive in MKN45; only p53 beta mRNA was detected in SGC7901; neither p53 beta nor Delta 133p53 mRNA was detected in KATO III. Delta 133p53 and p53 beta, which are possible indicators for the diagnosis and biological therapy of gastric carcinoma, were expressed differentially in different gastric tissues.
引用
收藏
页码:10468 / 10474
页数:7
相关论文
共 50 条
  • [1] The Δ133p53 Isoforms, Tuners of the p53 Pathway
    Joruiz, Sebastien M.
    Beck, Jessica A.
    Horikawa, Izumi
    Harris, Curtis C.
    CANCERS, 2020, 12 (11) : 1 - 20
  • [2] Influenza A Viruses Control Expression of Proviral Human p53 Isoforms p53β and Δ133p53α
    Terrier, Olivier
    Marcel, Virginie
    Cartet, Gaelle
    Lane, David P.
    Lina, Bruno
    Rosa-Calatrava, Manuel
    Bourdon, Jean-Christophe
    JOURNAL OF VIROLOGY, 2012, 86 (16) : 8452 - 8460
  • [3] p53 isoforms Δ133p53 and p53β are endogenous regulators of replicative cellular senescence
    Kaori Fujita
    Abdul M. Mondal
    Izumi Horikawa
    Giang H. Nguyen
    Kensuke Kumamoto
    Jane J. Sohn
    Elise D. Bowman
    Ewy A. Mathe
    Aaron J. Schetter
    Sharon R. Pine
    Helen Ji
    Borivoj Vojtesek
    Jean-Christophe Bourdon
    David P. Lane
    Curtis C. Harris
    Nature Cell Biology, 2009, 11 : 1135 - 1142
  • [4] p53 isoforms Δ133p53 and p53β are endogenous regulators of replicative cellular senescence
    Fujita, Kaori
    Mondal, Abdul M.
    Horikawa, Izumi
    Nguyen, Giang H.
    Kumamoto, Kensuke
    Sohn, Jane J.
    Bowman, Elise D.
    Mathe, Ewy A.
    Schetter, Aaron J.
    Pine, Sharon R.
    Ji, Helen
    Vojtesek, Borivoj
    Bourdon, Jean-Christophe
    Lane, David P.
    Harris, Curtis C.
    NATURE CELL BIOLOGY, 2009, 11 (09) : 1135 - U208
  • [5] p53 isoforms Δ133p53 and p53β are endogenous regulators of replicative cellular senescence
    Fujita, Kaori
    Mondal, Abdul M.
    Horikawa, Izumi
    Nguyen, Giang H.
    Kumamoto, Kensuke
    Sohn, Jane J.
    Bowman, Elise D.
    Mathe, A. Mathe
    Schetter, Aaron J.
    Pine, Sharon R.
    Ji, Helen
    Vojtesek, Borivoj
    Bourdon, Jean-Christophe
    Lane, David P.
    Harris, Curtis C.
    CANCER RESEARCH, 2010, 70
  • [6] Interaction of p53 with the Δ133p53α and Δ160p53α isoforms regulates p53 conformation and transcriptional activity
    Tomas, Fanny
    Roux, Pierre
    Gire, Veronique
    CELL DEATH & DISEASE, 2024, 15 (11):
  • [7] p53 isoforms, Δ133p53 and p53β, regulate aging-associated T lymphocyte senescence.
    Mondal, Abdul Matin
    Horikawa, Lzumi
    Pine, Sharon R.
    Fujita, Kaori
    Vojtesek, Borivoj
    Bourdon, Jean-Christophe
    Vera, Elsa
    Lane, David P.
    Blasco, Maria A.
    Harris, Curtis C.
    CANCER RESEARCH, 2011, 71
  • [8] The p53 isoform, Δ133p53α, stimulates angiogenesis and tumour progression
    Bernard, H.
    Garmy-Susini, B.
    Ainaoui, N.
    Van Den Berghe, L.
    Peurichard, A.
    Javerzat, S.
    Bikfalvi, A.
    Lane, D. P.
    Bourdon, J. C.
    Prats, A-C
    ONCOGENE, 2013, 32 (17) : 2150 - 2160
  • [9] The p53 isoform, Δ133p53α, stimulates angiogenesis and tumour progression
    H Bernard
    B Garmy-Susini
    N Ainaoui
    L Van Den Berghe
    A Peurichard
    S Javerzat
    A Bikfalvi
    D P Lane
    J C Bourdon
    A-C Prats
    Oncogene, 2013, 32 : 2150 - 2160
  • [10] Functional interplay between p53 and Δ133p53 in adaptive stress response
    Gong, Lu
    Pan, Xiao
    Abali, Gamze K.
    Little, John B.
    Yuan, Zhi-Min
    CELL DEATH AND DIFFERENTIATION, 2020, 27 (05): : 1618 - 1632