Landscape of G-quadruplex DNA structural regions in breast cancer.


Journal

Nature genetics
ISSN: 1546-1718
Titre abrégé: Nat Genet
Pays: United States
ID NLM: 9216904

Informations de publication

Date de publication:
09 2020
Historique:
received: 18 06 2019
accepted: 25 06 2020
pubmed: 5 8 2020
medline: 30 10 2020
entrez: 5 8 2020
Statut: ppublish

Résumé

Response and resistance to anticancer therapies vary due to intertumor and intratumor heterogeneity

Identifiants

pubmed: 32747825
doi: 10.1038/s41588-020-0672-8
pii: 10.1038/s41588-020-0672-8
doi:

Substances chimiques

Transcription Factors 0
DNA 9007-49-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

878-883

Subventions

Organisme : Wellcome Trust
ID : 209441/Z/17/Z
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C9681/A29214
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C14303/A17197
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C9681/A18618
Pays : United Kingdom

Références

Flavahan, W. A., Gaskell, E. & Bernstein, B. E. Epigenetic plasticity and the hallmarks of cancer. Science 357, eaal2380 (2017).
doi: 10.1126/science.aal2380
Curtis, C. et al. The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups. Nature 486, 346–352 (2012).
doi: 10.1038/nature10983
Rhodes, D. & Lipps, H. J. G-quadruplexes and their regulatory roles in biology. Nucleic Acids Res. 43, 8627–8637 (2015).
doi: 10.1093/nar/gkv862
Varshney, D., Spiegel, J., Zyner, K., Tannahill, D. & Balasubramanian, S. The regulation and functions of DNA and RNA G-quadruplexes. Nat. Rev. Mol. Cell Biol. https://doi.org/10.1038/s41580-020-0236-x (2020).
Marsico, G. et al. Whole genome experimental maps of DNA G-quadruplexes in multiple species. Nucleic Acids Res. 47, 3862–3874 (2019).
doi: 10.1093/nar/gkz179
Hänsel-Hertsch, R. et al. G-quadruplex structures mark human regulatory chromatin. Nat. Genet. 48, 1267–1272 (2016).
doi: 10.1038/ng.3662
Hänsel-Hertsch, R., Spiegel, J., Marsico, G., Tannahill, D. & Balasubramanian, S. Genome-wide mapping of endogenous G-quadruplex DNA structures by chromatin immunoprecipitation and high-throughput sequencing. Nat. Protoc. 13, 551–564 (2018).
doi: 10.1038/nprot.2017.150
Hänsel-Hertsch, R., Di Antonio, M. & Balasubramanian, S. DNA G-quadruplexes in the human genome: detection, functions and therapeutic potential. Nat. Rev. Mol. Cell Biol. 18, 279–284 (2017).
doi: 10.1038/nrm.2017.3
Paeschke, K., Capra, J. A. & Zakian, V. A. DNA replication through G-quadruplex motifs is promoted by the Saccharomyces cerevisiae Pif1 DNA helicase. Cell 145, 678–691 (2011).
doi: 10.1016/j.cell.2011.04.015
Cheung, I., Schertzer, M., Rose, A. & Lansdorp, P. M. Disruption of dog-1 in Caenorhabditis elegans triggers deletions upstream of guanine-rich DNA. Nat. Genet. 31, 405–409 (2002).
doi: 10.1038/ng928
Georgakopoulos-Soares, I., Morganella, S., Jain, N., Hemberg, M. & Nik-Zainal, S. Noncanonical secondary structures arising from non-B DNA motifs are determinants of mutagenesis. Genome Res. 28, 1264–1271 (2018).
doi: 10.1101/gr.231688.117
Lensing, S. V. et al. DSBCapture: in situ capture and sequencing of DNA breaks. Nat. Methods 13, 855–857 (2016).
doi: 10.1038/nmeth.3960
Bouwman, B. A. M. & Crosetto, N. Endogenous DNA double-strand breaks during DNA transactions: emerging insights and methods for genome-wide profiling. Genes (Basel) 9, 632 (2018).
doi: 10.3390/genes9120632
De, S. & Michor, F. DNA secondary structures and epigenetic determinants of cancer genome evolution. Nat. Struct. Mol. Biol. 18, 950–955 (2011).
doi: 10.1038/nsmb.2089
Chambers, V. S. et al. High-throughput sequencing of DNA G-quadruplex structures in the human genome. Nat. Biotechnol. 33, 1–7 (2015).
doi: 10.1038/nbt.3295
Pereira, B. et al. The somatic mutation profiles of 2,433 breast cancers refine their genomic and transcriptomic landscapes. Nat. Commun. 7, 11479 (2016).
doi: 10.1038/ncomms11479
Bruna, A. et al. A biobank of breast cancer explants with preserved intra-tumor heterogeneity to screen anticancer compounds. Cell 167, 260–274.e22 (2016).
doi: 10.1016/j.cell.2016.08.041
Rueda, O. M. et al. Dynamics of breast-cancer relapse reveal late-recurring ER-positive genomic subgroups. Nature 567, 399–404 (2019).
doi: 10.1038/s41586-019-1007-8
Orlando, D. A. et al. Quantitative ChIP–Seq normalization reveals global modulation of the epigenome. Cell Rep. 9, 1163–1170 (2014).
doi: 10.1016/j.celrep.2014.10.018
Scheinin, I. et al. DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly. Genome Res. 24, 2022–2032 (2014).
doi: 10.1101/gr.175141.114
Mao, S.-Q. et al. DNA G-quadruplex structures mold the DNA methylome. Nat. Struct. Mol. Biol. 25, 951–957 (2018).
doi: 10.1038/s41594-018-0131-8
Zaret, K. S. & Carroll, J. S. Pioneer transcription factors: establishing competence for gene expression. Genes Dev. 25, 2227–2241 (2011).
doi: 10.1101/gad.176826.111
Gertz, J. et al. Distinct properties of cell-type-specific and shared transcription factor binding sites. Mol. Cell 52, 25–36 (2013).
doi: 10.1016/j.molcel.2013.08.037
Oki, S. et al. ChIP‐Atlas: a data‐mining suite powered by full integration of public ChIP–seq data. EMBO Rep. 19, e46255 (2018).
doi: 10.15252/embr.201846255
Rodriguez, R. et al. A novel small molecule that alters shelterin integrity and triggers a DNA-damage response at telomeres. J. Am. Chem. Soc. 130, 15758–15759 (2008).
doi: 10.1021/ja805615w
Xu, H. et al. CX-5461 is a DNA G-quadruplex stabilizer with selective lethality in BRCA1/2 deficient tumours. Nat. Commun. 8, 14432 (2017).
doi: 10.1038/ncomms14432
Biffi, G., Tannahill, D., Miller, J., Howat, W. J. & Balasubramanian, S. Elevated levels of G-quadruplex formation in human stomach and liver cancer tissues. PLoS One 9, e102711 (2014).
doi: 10.1371/journal.pone.0102711
McLuckie, K. I. E. et al. G-quadruplex DNA as a molecular target for induced synthetic lethality in cancer cells. J. Am. Chem. Soc. 135, 9640–9643 (2013).
doi: 10.1021/ja404868t
Zimmer, J. et al. Targeting BRCA1 and BRCA2 deficiencies with G-quadruplex-interacting compounds. Mol. Cell 61, 449–460 (2016).
doi: 10.1016/j.molcel.2015.12.004
Schmidt, D. et al. ChIP–seq: using high-throughput sequencing to discover protein–DNA interactions. Methods 48, 240–248 (2009).
doi: 10.1016/j.ymeth.2009.03.001
Biffi, G., Tannahill, D., McCafferty, J. & Balasubramanian, S. Quantitative visualization of DNA G-quadruplex structures in human cells. Nat. Chem. 5, 182–186 (2013).
doi: 10.1038/nchem.1548
Li, H. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. Preprint at https://arxiv.org/abs/1303.3997 (2013).
Robinson, M. D., McCarthy, D. J. & Smyth, G. K. edgeR: a bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics 26, 139–140 (2010).
doi: 10.1093/bioinformatics/btp616
Khan, A. & Mathelier, A. Intervene: a tool for intersection and visualization of multiple gene or genomic region sets. BMC Bioinformatics 18, 287 (2017).
doi: 10.1186/s12859-017-1708-7
Chin, S.-F. et al. Shallow whole genome sequencing for robust copy number profiling of formalin-fixed paraffin-embedded breast cancers. Exp. Mol. Pathol. 104, 161–169 (2018).
doi: 10.1016/j.yexmp.2018.03.006
Huang, W., Loganantharaj, R., Schroeder, B., Fargo, D. & Li, L. PAVIS: a tool for peak annotation and visualization. Bioinformatics 29, 3097–3099 (2013).
doi: 10.1093/bioinformatics/btt520
Le, D. D., Di Antonio, M., Chan, L. K. M. & Balasubramanian, S. G-quadruplex ligands exhibit differential G-tetrad selectivity. Chem. Commun. (Camb.) 51, 8048–8050 (2015).
doi: 10.1039/C5CC02252E

Auteurs

Robert Hänsel-Hertsch (R)

Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany.
Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne and University Hospital Cologne, Cologne, Germany.
Institute of Human Genetics, University Hospital Cologne, Cologne, Germany.
Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.

Angela Simeone (A)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.

Abigail Shea (A)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.

Winnie W I Hui (WWI)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.

Katherine G Zyner (KG)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.

Giovanni Marsico (G)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.
Inivata, Babraham Research Campus, Cambridge, UK.

Oscar M Rueda (OM)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.

Alejandra Bruna (A)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.
The Institute of Cancer Research, London, UK.

Alistair Martin (A)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.

Xiaoyun Zhang (X)

Department of Chemistry, University of Cambridge, Cambridge, UK.

Santosh Adhikari (S)

Department of Chemistry, University of Cambridge, Cambridge, UK.

David Tannahill (D)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.

Carlos Caldas (C)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.
Cambridge Breast Cancer Research Unit, Cambridge University Hospital NHS Foundation Trust, Cambridge, UK.
Cancer Research UK Cambridge Centre, NIHR Cambridge Biomedical Research Centre and Cambridge Experimental Cancer Medicine Centre, Cambridge University Hospital NHS Foundation Trust, Cambridge, UK.

Shankar Balasubramanian (S)

Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK. sb10031@cam.ac.uk.
Department of Chemistry, University of Cambridge, Cambridge, UK. sb10031@cam.ac.uk.
School of Clinical Medicine, University of Cambridge, Cambridge, UK. sb10031@cam.ac.uk.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH