Progress Toward Epigenetic Targeted Therapies for Childhood Cancer

被引:0
作者
Liapodimitri, Athanasia [1 ]
Tetens, Ashley R. [1 ]
Craig-Schwartz, Jordyn [1 ]
Lunsford, Kayleigh [1 ]
Skalitzky, Kegan O. [1 ]
Koldobskiy, Michael A. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Oncol, Div Pediat Oncol, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Sch Med, Baltimore, MD 21287 USA
关键词
epigenetics; pediatric cancer; DNA methylation; histone modifications; epigenetic therapy; ACUTE MYELOID-LEUKEMIA; HISTONE DEACETYLASE INHIBITOR; ACUTE LYMPHOBLASTIC-LEUKEMIA; INTRINSIC PONTINE GLIOMA; T-CELL LYMPHOMA; GENE-EXPRESSION; PHASE-II; THERAPEUTIC TARGET; SOMATIC MUTATIONS; CHEMICAL PROBE;
D O I
10.3390/cancers16244149
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Among the most significant discoveries from cancer genomics efforts has been the critical role of epigenetic dysregulation in cancer development and progression. Studies across diverse cancer types have revealed frequent mutations in genes encoding epigenetic regulators, alterations in DNA methylation and histone modifications, and a dramatic reorganization of chromatin structure. Epigenetic changes are especially relevant to pediatric cancers, which are often characterized by a low rate of genetic mutations. The inherent reversibility of epigenetic lesions has led to an intense interest in the development of epigenetic targeted therapies. Additionally, the recent appreciation of the interplay between the epigenome and immune regulation has sparked interest in combination therapies and synergistic immunotherapy approaches. Further, the recent appreciation of epigenetic variability as a driving force in cancer evolution has suggested new roles for epigenetic therapies in limiting plasticity and resistance. Here, we review recent progress and emerging directions in the development of epigenetic targeted therapeutics and their promise across the landscape of childhood cancers.
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共 243 条
[1]   Genetic characterization of TET1, TET2, and TET3 alterations in myeloid malignancies [J].
Abdel-Wahab, Omar ;
Mullally, Ann ;
Hedvat, Cyrus ;
Garcia-Manero, Guillermo ;
Patel, Jay ;
Wadleigh, Martha ;
Malinge, Sebastien ;
Yao, JinJuan ;
Kilpivaara, Outi ;
Bhat, Rukhmi ;
Huberman, Kety ;
Thomas, Sabrena ;
Dolgalev, Igor ;
Heguy, Adriana ;
Paietta, Elisabeth ;
Le Beau, Michelle M. ;
Beran, Miloslav ;
Tallman, Martin S. ;
Ebert, Benjamin L. ;
Kantarjian, Hagop M. ;
Stone, Richard M. ;
Gilliland, D. Gary ;
Crispino, John D. ;
Levine, Ross L. .
BLOOD, 2009, 114 (01) :144-147
[2]   The KDM4/JMJD2 histone demethylases are required for hematopoietic stem cell maintenance [J].
Agger, Karl ;
Nishimura, Koutarou ;
Miyagi, Satoru ;
Messling, Jan-Erik ;
Rasmussen, Kasper Dindler ;
Helin, Kristian .
BLOOD, 2019, 134 (14) :1154-1158
[3]   Targeting EZH2-mediated methylation of histone 3 inhibits proliferation of pediatric acute monocytic leukemia cells in vitro [J].
Al-Ghabkari, Abdulhameed ;
Narendran, Aru .
CANCER BIOLOGY & THERAPY, 2021, 22 (04) :333-344
[4]   Inhibition of EZH2 suppresses self-renewal and induces radiation sensitivity in atypical rhabdoid teratoid tumor cells [J].
Alimova, Irina ;
Birks, Diane K. ;
Harris, Peter S. ;
Knipstein, Jeffrey A. ;
Venkataraman, Sujatha ;
Marquez, Victor E. ;
Foreman, Nicholas K. ;
Vibhakar, Rajeev .
NEURO-ONCOLOGY, 2013, 15 (02) :149-160
[5]   TET family dioxygenases and DNA demethylation in stem cells and cancers [J].
An, Jungeun ;
Rao, Anjana ;
Ko, Myunggon .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2017, 49 :e323-e323
[6]   Acute loss of TET function results in aggressive myeloid cancer in mice [J].
An, Jungeun ;
Gonzalez-Avalos, Edahi ;
Chawla, Ashu ;
Jeong, Mira ;
Lopez-Moyado, Isaac F. ;
Li, Wei ;
Goodell, Margaret A. ;
Chavez, Lukas ;
Ko, Myunggon ;
Rao, Anjana .
NATURE COMMUNICATIONS, 2015, 6
[7]   Evolution of Neoantigen Landscape during Immune Checkpoint Blockade in Non-Small Cell Lung Cancer [J].
Anagnostou, Valsamo ;
Smith, Kellie N. ;
Forde, Patrick M. ;
Niknafs, Noushin ;
Bhattacharya, Rohit ;
White, James ;
Zhang, Theresa ;
Adleff, Vilmos ;
Phallen, Jillian ;
Wali, Neha ;
Hruban, Carolyn ;
Guthrie, Violeta B. ;
Rodgers, Kristen ;
Naidoo, Jarushka ;
Kang, Hyunseok ;
Sharfman, William ;
Georgiades, Christos ;
Verde, Franco ;
Illei, Peter ;
Li, Qing Kay ;
Gabrielson, Edward ;
Brock, Malcolm V. ;
Zahnow, Cynthia A. ;
Baylin, Stephen B. ;
Scharpf, Robert B. ;
Brahmer, Julie R. ;
Karchin, Rachel ;
Pardoll, Drew M. ;
Velculescu, Victor E. .
CANCER DISCOVERY, 2017, 7 (03) :264-276
[8]   Re-programing Chromatin with a Bifunctional LSD1/HDAC Inhibitor Induces Therapeutic Differentiation in DIPG [J].
Anastas, Jamie N. ;
Zee, Barry M. ;
Kalin, Jay H. ;
Kim, Mirhee ;
Guo, Robyn ;
Alexandrescu, Sanda ;
Blanco, Mario Andres ;
Giera, Stefanie ;
Gillespie, Shawn M. ;
Das, Jayanta ;
Wu, Muzhou ;
Nocco, Sarah ;
Bonal, Dennis M. ;
Quang-De Nguyen ;
Suva, Mario L. ;
Bernstein, Bradley E. ;
Alani, Rhoda ;
Golub, Todd R. ;
Cole, Philip A. ;
Filbin, Mariella G. ;
Shi, Yang .
CANCER CELL, 2019, 36 (05) :528-+
[9]   Pharmacologic inhibition of lysine-specific demethylase 1 as a therapeutic and immune-sensitization strategy in pediatric high-grade glioma [J].
Bailey, Cavan P. ;
Figueroa, Mary ;
Gangadharan, Achintyan ;
Yang, Yanwen ;
Romero, Megan M. ;
Kennis, Bridget A. ;
Yadavilli, Sridevi ;
Henry, Verlene ;
Collier, Tiara ;
Monje, Michelle ;
Lee, Dean A. ;
Wang, Linghua ;
Nazarian, Javad ;
Gopalakrishnan, Vidya ;
Zaky, Wafik ;
Becher, Oren J. ;
Chandra, Joya .
NEURO-ONCOLOGY, 2020, 22 (09) :1302-1314
[10]   The heterogeneity of pediatric MLL-rearranged acute myeloid leukemia [J].
Balgobind, B. V. ;
Zwaan, C. M. ;
Pieters, R. ;
Van den Heuvel-Eibrink, M. M. .
LEUKEMIA, 2011, 25 (08) :1239-1248