Targeting MDM4 as a Novel Therapeutic Approach for Hematologic Malignancies

被引:2
作者
Cao, Lei [1 ]
Fan, Lei [1 ]
Xu, Wei [1 ]
Li, Jian-Yong [1 ]
机构
[1] Nanjing Med Univ, Jiangsu Prov Hosp, Affiliated Hosp 1, Dept Hematol, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomarker; hematologic malignancies; MDM2; MDM4; p53; therapeutic approach; ACUTE MYELOID-LEUKEMIA; BREAST-CANCER CELLS; CHRONIC LYMPHOCYTIC-LEUKEMIA; TUMOR-SUPPRESSOR ACTIVITY; UBIQUITIN LIGASE ACTIVITY; ESTROGEN-RECEPTOR-ALPHA; ACTIVITY IN-VIVO; P53; ACTIVITY; ACTIVATE P53; DNA-DAMAGE;
D O I
10.2174/156800961509151110124616
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mouse double minute 4 (MDM4) as a member of MDM family, is an oncogene emerging as an imperative negative regulator of p53. Tumor suppressor protein p53 plays a crucial role in cell cycle arrest, apoptosis and homeostasis. It has been reported that frequent inactivation of p53 was observed in numerous human cancers including hematologic malignancies. MDM4, the newly discovered modulator of p53 protein, is frequently amplified in various solid tumors such as cutaneous melanoma, retinoblastoma and hematological malignances such as chronic lymphocytic leukemia, acute myeloid leukemia and mantle cell lymphoma. Multiple evidences implicate that over-expression of MDM4 is associated with tumor progression and poor prognosis which can be reversed by knockdown of MDM4 expression or restoration of p53 function, and support the rationale for the design of future MDM4-specific therapeutics. This article discusses and focuses on using MDM4 as a novel biomarker as well as a therapeutic target for hematologic malignancies.
引用
收藏
页码:769 / 780
页数:12
相关论文
共 115 条
  • [1] Mdm2 binds to Nbs1 at sites of DNA damage and regulates double strand break repair
    Alt, JR
    Bouska, A
    Fernandez, MR
    Cerny, RL
    Xiao, H
    Eischen, CM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (19) : 18771 - 18781
  • [2] Mdm2 and Mdm4 loss regulates distinct p53 activities
    Barboza, Juan A.
    Iwakuma, Tomoo
    Terzian, Tamara
    El-Naggar, Adel K.
    Lozano, Guillermina
    [J]. MOLECULAR CANCER RESEARCH, 2008, 6 (06) : 947 - 954
  • [3] Bardot B., 2014, ONCOGENE
  • [4] Significance of HDMX-S (or MDM4) mRNA splice variant overexpression and HDMX gene amplification on primary soft tissue sarcoma prognosis
    Bartel, F
    Schulz, J
    Böhnke, A
    Blümke, K
    Kappler, M
    Bache, M
    Schmidt, H
    Würl, P
    Taubert, H
    Hauptmann, S
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2005, 117 (03) : 469 - 475
  • [5] On the Mechanism of Action of SJ-172550 in Inhibiting the Interaction of MDM4 and p53
    Bista, Michal
    Smithson, David
    Pecak, Aleksandra
    Salinas, Gabriella
    Pustelny, Katarzyna
    Min, Jaeki
    Pirog, Artur
    Finch, Kristin
    Zdzalik, Michal
    Waddell, Brett
    Wladyka, Benedykt
    Kedracka-Krok, Sylwia
    Dyer, Michael A.
    Dubin, Grzegorz
    Guy, R. Kiplin
    [J]. PLOS ONE, 2012, 7 (06):
  • [6] Fragment-Based Library Generation for the Discovery of a Peptidomimetic p53-Mdm4 Inhibitor
    Boltjes, Andre
    Huang, Yijun
    van de Velde, Rob
    Rijkee, Laurie
    Wolf, Siglinde
    Gaugler, James
    Lesniak, Katarzyna
    Guzik, Katarzyna
    Holak, Tad A.
    Domling, Alexander
    [J]. ACS COMBINATORIAL SCIENCE, 2014, 16 (08) : 393 - 396
  • [7] Stapled Peptides with Improved Potency and Specificity That Activate p53
    Brown, Christopher J.
    Quah, Soo T.
    Jong, Janice
    Goh, Amanda M.
    Chiam, Poh C.
    Khoo, Kian H.
    Choong, Meng L.
    Lee, May A.
    Yurlova, Larisa
    Zolghadr, Kourosh
    Joseph, Thomas L.
    Verma, Chandra S.
    Lane, David P.
    [J]. ACS CHEMICAL BIOLOGY, 2013, 8 (03) : 506 - 512
  • [8] Stapled α-helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53-dependent cancer therapy
    Chang, Yong S.
    Graves, Bradford
    Guerlavais, Vincent
    Tovar, Christian
    Packman, Kathryn
    To, Kwong-Him
    Olson, Karen A.
    Kesavan, Kamala
    Gangurde, Pranoti
    Mukherjee, Aditi
    Baker, Theresa
    Darlak, Krzysztof
    Elkin, Carl
    Filipovic, Zoran
    Qureshi, Farooq Z.
    Cai, Hongliang
    Berry, Pamela
    Feyfant, Eric
    Shi, Xiangguo E.
    Horstick, James
    Annis, D. Allen
    Manning, Anthony M.
    Fotouhi, Nader
    Nash, Huw
    Vassilev, Lyubomir T.
    Sawyer, Tomi K.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (36) : E3445 - E3454
  • [9] NUMB controls p53 tumour suppressor activity
    Colaluca, Ivan N.
    Tosoni, Daniela
    Nuciforo, Paolo
    Senic-Matuglia, Francesca
    Galimberti, Viviana
    Viale, Giuseppe
    Pece, Salvatore
    Di Fiore, Pier Paolo
    [J]. NATURE, 2008, 451 (7174) : 76 - U11
  • [10] MDM4 (MDMX) is overexpressed in chronic lymphocytic leukaemia (CLL) and marks a subset of p53wild-type CLL with a poor cytotoxic response to Nutlin-3
    Dal Bo, Michele
    Secchiero, Paola
    Degan, Massimo
    Marconi, Daniela
    Bomben, Riccardo
    Pozzato, Gabriele
    Gaidano, Gianluca
    Del Poeta, Giovanni
    Forconi, Francesco
    Zauli, Giorgio
    Gattei, Valter
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2010, 150 (02) : 237 - 239