Cisplatin Sensitivity Mediated by WEE1 and CHK1 Is Mediated by miR-155 and the miR-15 Family

被引:81
|
作者
Pouliot, Lynn M. [1 ,2 ]
Chen, Yu-Chi [3 ]
Bai, Jennifer [1 ]
Guha, Rajarshi [3 ]
Martin, Scott E. [3 ]
Gottesman, Michael M. [1 ]
Hall, Matthew D. [1 ]
机构
[1] NCI, Cell Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] Georgetown Univ, Dept Microbiol & Immunol, Washington, DC USA
[3] NIH, RNAi Screening Facil, Natl Ctr Adv Translat Sci, Rockville, MD USA
基金
美国国家卫生研究院;
关键词
P53-DEFICIENT TUMOR-CELLS; DNA-DAMAGING AGENTS; MULTIDRUG-RESISTANCE; CHECKPOINT KINASE-1; REDUCED EXPRESSION; OVARIAN-CANCER; MICRORNA; PROTEINS; TARGET; ACCUMULATION;
D O I
10.1158/0008-5472.CAN-12-1400
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Resistance to platinum-based therapies arises by multiple mechanisms, including by alterations to cell-cycle kinases that mediate G(2)-M phase arrest. In this study, we conducted parallel high-throughput screens for microRNAs (miRNA) that could restore sensitivity to cisplatin-resistant cells, and we screened for kinases targeted by miRNAs that mediated cisplatin resistance. Overexpression of the cell-cycle kinases WEE1 and CHK1 occurred commonly in cisplatin-resistant cells. miRNAs in the miR-15/16/195/424/497 family were found to sensitize cisplatin-resistant cells to apoptosis by targeting WEE1 and CHK1. Loss-of-function and gain-of-function studies showed that miR-15 family members controlled the expression of WEE1 and CHK1. Supporting these results, we found that in the presence of cisplatin altering expression of miR-16 or related genes altered cell cycle distribution. Our findings reveal critical regulation of miRNAs and their cell-cycle-associated kinase targets in mediating resistance to cisplatin. Cancer Res; 72(22); 5945-55. (C) 2012 AACR.
引用
收藏
页码:5945 / 5955
页数:11
相关论文
共 50 条
  • [1] Loss of miR-155 upregulates WEE1 in metastatic melanoma
    DiSano, Julie A.
    Huffnagle, Ian
    Gowda, Raghavendra
    Spiegelman, Vladimir S.
    Robertson, Gavin P.
    Pameijer, Colette R.
    MELANOMA RESEARCH, 2019, 29 (02) : 216 - 219
  • [2] Combined inhibition of Chk1 and Wee1 kinases for cancer treatment
    Hauge, S.
    Hasvold, G.
    Joel, M.
    Naucke, C.
    Rodland, G. E.
    Syljuasen, R. G.
    RADIOTHERAPY AND ONCOLOGY, 2016, 119 : S478 - S478
  • [3] miR-16 and miR-26a target checkpoint kinases Wee1 and Chk1 in response to p53 activation by genotoxic stress
    L Lezina
    N Purmessur
    A V Antonov
    T Ivanova
    E Karpova
    K Krishan
    M Ivan
    V Aksenova
    D Tentler
    A V Garabadgiu
    G Melino
    N A Barlev
    Cell Death & Disease, 2013, 4 : e953 - e953
  • [4] miR-16 and miR-26a target checkpoint kinases Wee1 and Chk1 in response to p53 activation by genotoxic stress
    Lezina, L.
    Purmessur, N.
    Antonov, A. V.
    Ivanova, T.
    Karpova, E.
    Krishan, K.
    Ivan, M.
    Aksenova, V.
    Tentler, D.
    Garabadgiu, A. V.
    Melino, G.
    Barlev, N. A.
    CELL DEATH & DISEASE, 2013, 4 : e953 - e953
  • [5] A siRNA high-throughput screening identified Wee1 as determinant of Chk1 inhibitor sensitivity
    Carrassa, Laura
    Chila, Rosaria
    Lupi, Monica
    Ricci, Francesca
    Mazzoletti, Marco
    Celenza, Cinzia
    Broggini, Massimo
    Damia, Giovanna
    CANCER RESEARCH, 2012, 72
  • [6] Therapeutic targeting of the DNA damage mediators CHK1 and Wee1 in neuroblastoma
    Russell, Mike
    Levin, Kirill
    Rader, JulieAnn
    Toniatti, Carlo
    Maris, John M.
    Cole, Kristina A.
    CANCER RESEARCH, 2012, 72
  • [7] Combined inhibition of Wee1 and Chk1 as a therapeutic strategy in multiple myeloma
    Bruyer, Angelique
    Dutrieux, Laure
    de Boussac, Hugues
    Martin, Thibaut
    Chemlal, Djamila
    Robert, Nicolas
    Requirand, Guilhem
    Cartron, Guillaume
    Vincent, Laure
    Herbaux, Charles
    Lutzmann, Malik
    Bret, Caroline
    Pasero, Philippe
    Moreaux, Jerome
    Ovejero, Sara
    FRONTIERS IN ONCOLOGY, 2023, 13
  • [8] Synergism Through WEE1 and CHK1 Inhibition in Acute Lymphoblastic Leukemia
    Di Rora, Andrea Ghelli Luserna
    Bocconcelli, Matteo
    Ferrari, Anna
    Terragna, Carolina
    Bruno, Samantha
    Imbrogno, Enrica
    Beeharry, Neil
    Robustelli, Valentina
    Ghetti, Martina
    Napolitano, Roberta
    Chirumbolo, Gabriella
    Marconi, Giovanni
    Papayannidis, Cristina
    Paolini, Stefania
    Sartor, Chiara
    Simonetti, Giorgia
    Yen, Timothy J.
    Martinelli, Giovanni
    CANCERS, 2019, 11 (11)
  • [9] Inhibition of Chk1 and Wee1 as a new therapeutic approach in Mantle Cell Lymphoma
    Carrassa, Laura
    Chila, Rosaria
    Basana, Alessandra
    Ricci, Francesca
    Guffanti, Federica
    Lupi, Monica
    Rinaldi, Andrea
    Cascione, Luciano
    Bertoni, Francesco
    Broggini, Massimo
    Damia, Giovanna
    CANCER RESEARCH, 2014, 74 (19)
  • [10] Chk1 inhibition and Wee1 inhibition combine synergistically to impede cellular proliferation
    Davies, Kurtis D.
    Cable, P. LouAnn
    Garrus, Jennifer E.
    Sullivan, Francis X.
    von Carlowitz, Ira
    Le Huerou, Yvan
    Wallace, Eli
    Woessner, Richard D.
    Gross, Stefan
    CANCER BIOLOGY & THERAPY, 2011, 12 (09) : 788 - 796