Nuclear ING2 expression is reduced in osteosarcoma

被引:9
|
作者
Han, Xiao-Rui [1 ]
Bai, Xi-Zhuang [1 ]
Sun, Yu [1 ]
Yang, Yan [1 ]
机构
[1] China Med Univ, Affiliated Hosp 1, Dept Joint Surg & Sports Med, Shenyang 110001, Liaoning, Peoples R China
关键词
inhibitor of growth 2; osteosarcoma; cell cycle; apoptosis; senescence; HUMAN-CELLS; PHD-FINGER; PROTEIN; GENE; P53; ACETYLATION; CARCINOMA;
D O I
10.3892/or.2014.3458
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma is a high-grade malignant bone tumor. Loss of inhibitor of growth 2 (ING2) expression has been demonstrated in numerous types of cancers. However, no study has shown the relationship between ING2 expression and osteosarcoma. In the present study, we confirmed that the levels of ING2 mRNA and protein were lower in cancer tissues than these levels in normal tissues. Loss of nuclear ING2 protein was significantly associated with a decreased survival time of patients. Osteosarcoma cells were transfected with ING2 protein without a nuclear localization signal or intact ING2 protein to examine the effects of exogenous expression of ING2 in vitro. Compared to the control cells, intact ING2-expressing cells exhibited increased apoptosis, G1 phase arrest and senescence. Taken together, these results suggest that ING2 acts as a tumor suppressor in osteosarcoma.
引用
收藏
页码:1967 / 1972
页数:6
相关论文
共 50 条
  • [41] ING2 tumor suppressive protein translocates into mitochondria and is involved in cellular metabolism homeostasis
    Ricordel, Charles
    Chaillot, Laura
    Blondel, Alice
    Archambeau, Jerome
    Jouan, Florence
    Mouche, Audrey
    Tiercin, Marie
    Burel, Agnes
    Lena, Herve
    Desrues, Benoit
    Guillaudeux, Thierry
    Pedeux, Remy
    ONCOGENE, 2021, 40 (24) : 4111 - 4123
  • [42] ING2 tumor suppressive protein translocates into mitochondria and is involved in cellular metabolism homeostasis
    Charles Ricordel
    Laura Chaillot
    Alice Blondel
    Jérôme Archambeau
    Florence Jouan
    Audrey Mouche
    Marie Tiercin
    Agnès Burel
    Hervé Lena
    Benoît Desrues
    Thierry Guillaudeux
    Rémy Pedeux
    Oncogene, 2021, 40 : 4111 - 4123
  • [43] ING2 as a novel mediator of transforming growth factor-β-dependent responses in epithelial cells
    Sarker, Krishna P.
    Kataoka, Hiromi
    Chan, Angela
    Netherton, Stuart J.
    Pot, Isabelle
    Huynh, Mai Anh
    Feng, Xiaolan
    Bonni, Azad
    Riabowol, Karl
    Bonni, Shirin
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (19) : 13269 - 13279
  • [44] Targeted Disruption of Ing2 Results in Defective Spermatogenesis and Development of Soft-Tissue Sarcomas
    Saito, Motonobu
    Kumamoto, Kensuke
    Robles, Ana I.
    Horikawa, Izumi
    Furusato, Bungo
    Okamura, Shu
    Goto, Akiteru
    Yamashita, Taro
    Nagashima, Makoto
    Lee, Tin-Lap
    Baxendale, Vanessa J.
    Rennert, Owen M.
    Takenoshita, Seiichi
    Yokota, Jun
    Sesterhenn, Isabell A.
    Trivers, Glenwood E.
    Hussain, S. Perwez
    Harris, Curtis C.
    PLOS ONE, 2010, 5 (11):
  • [45] Multiple variants of the ING1 and ING2 tumor suppressors are differentially expressed and thyroid hormone-responsive in Xenopus laevis
    Wagner, MJ
    Helbing, CC
    GENERAL AND COMPARATIVE ENDOCRINOLOGY, 2005, 144 (01) : 38 - 50
  • [46] Antithetic hTERT Regulation by Androgens in Prostate Cancer Cells: hTERT Inhibition Is Mediated by the ING1 and ING2 Tumor Suppressors
    Bartsch, Sophie
    Mirzakhani, Kimia
    Neubert, Laura
    Stenzel, Alexander
    Ehsani, Marzieh
    Esmaeili, Mohsen
    Pungsrinont, Thanakorn
    Kacal, Merve
    Rasa, Seyed Mohammad Mahdi
    Kallenbach, Julia
    Damodaran, Divya
    Ribaudo, Federico
    Grimm, Marc-Oliver
    Neri, Francesco
    Baniahmad, Aria
    CANCERS, 2021, 13 (16)
  • [47] HECT ubiquitin ligase Smurf1 targets the tumor suppressor ING2 for ubiquitination and degradation
    Nie, Jing
    Liu, Lin
    Wu, Min
    Xing, Guichun
    He, Shan
    Yin, Yuxin
    Tian, Chunyan
    He, Fuchu
    Zhang, Lingqiang
    FEBS LETTERS, 2010, 584 (14) : 3005 - 3012
  • [48] The Tumor Suppressive Protein ING2 is Required for DNA Damage Response Proteins Recruitment and Promotes NHEJ
    Guerillon, C.
    Larrieu, D.
    Mourcin, F.
    Brambilla, C.
    Sengupta, S.
    Pedeux, R.
    EUROPEAN JOURNAL OF CANCER, 2012, 48 : S126 - S126
  • [49] Exploiting ING2 Epigenetic Modulation as a Therapeutic Opportunity for Non-Small Cell Lung Cancer
    Blondel, Alice
    Benberghout, Amine
    Pedeux, Remy
    Ricordel, Charles
    CANCERS, 2019, 11 (10)
  • [50] ING2 loss sensitizes KRAS-mutated NSCLC to WEE1 inhibition through regulation of CHK1 expression.
    Ricordel, Charles
    Thalappilly, Subash
    Archambeau, Jerome
    Chan, Angela
    Nixon, Nancy
    Desrues, Benoit
    Bebb, Gwyn
    Riabowol, Karl
    Pedeux, Remy
    MOLECULAR CANCER RESEARCH, 2020, 18 (05) : 57 - 57