This competing renewal of an NCI MERIT Award follows an extremely productive period with over 50 high- impact publications. We now plan to follow up on 3 sets of major cancer epigenetics discoveries of the past 3 years, joining forces with a leader in mutational analysis of cancer progression to explore the relationship and mechanistic links between genetic and epigenetic change in pancreatic cancer progression. The first of these discoveries is that most altered DNA methylation in cancer is not at CpG islands but at nearby regions we termed "CpG island shores," and that most of the disrupted methylation in cancer involves the same sequences that normally distinguish tissues during normal development. The second discovery came from whole-genome bisulfite sequencing (WGBS) of cancer and matched normal tissue and revealed that: (i) the island and shore methylation involves loss of stability of boundaries between high and low methylation at CpG islands;and (ii) previously unknown large contiguous hypomethylated blocks involving 1/3 of single copy genes, leading to hypervariable gene expression. The third discovery was of large organized chromatin lysine (K) modifications or "LOCKs" that regulate heterochromatin during normal development, and that these chromatin LOCKs correspond to the large hypomethylated blocks in cancer. Furthermore, the LOCKs are dynamically reprogrammed during epithelial-mesenchymal transition (EMT), which is critical for cancer progression. We will follow up these discoveries in three Aims: (1) We will determine the extent to which classes of altered DNA methylation correspond to clonal evolution in human cancer, using pancreatic cancer as a model. We will identify methylation founders, drivers and passengers, performing low-pass whole genome bisulfite sequencing (WGBS) initially on 100 samples from 10 patients, in sections of pancreatic tumors and matched metastases representing subclonal evolution and progression, which have also been subjected to DNA sequencing for mutations. We will also investigate epigenetic mediators of mutation in pancreatic cancer, using statistical mediation analysis. (2) We will investigate the relationship between chromatin and DNA methylation during neoplastic transformation and malignant progression, including EMT. We will perform ChIPSeq for chromatin LOCKs on pancreatic cancers on 100 samples from Aim 1, as well as capture bisulfite sequencing on 500 samples from 100 patients, and motif analysis to identify proteins regulating epigenetic disruption and epigenetic mediation of mutation. (3) We will perform functional analysis of epigenetic targets and mediators from Aim 2, including microfluidic modeling and in situ analysis. With expert collaborators, we have included methods to analyze migrating mesenchymal-like cells, complemented with a new approach to in situ gene-specific chromatin analysis, comparing stable EMT-like and well-differentiated metastases from the same cancers of the same patients. Overall, the work in this grant addresses some of the deepest problems in cancer epigenetics, identifying both sequences and trans-acting factors that control epigenetic instability during cancer progression.

Public Health Relevance

This competing renewal of an NCI MERIT Award addresses the role in cancer of the epigenome, or changes controlling gene expression other than the DNA sequence itself. The work will identify epigenetic drivers of tumor progression, focusing on pancreatic cancer, identifying disruptions in DNA sequences and trans-acting regulatory factors that cause epigenetic instability, contributing to cancer metastasis and resistance to treatment. The work in this grant can help to define a new paradigm for cancer diagnosis and treatment targeted to the epigenome.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA054358-20A1
Application #
8580450
Study Section
Cancer Genetics Study Section (CG)
Program Officer
Okano, Paul
Project Start
1991-05-01
Project End
2018-06-30
Budget Start
2013-08-15
Budget End
2014-06-30
Support Year
20
Fiscal Year
2013
Total Cost
$448,307
Indirect Cost
$171,574
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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Hansen, Kasper D; Sabunciyan, Sarven; Langmead, Ben et al. (2014) Large-scale hypomethylated blocks associated with Epstein-Barr virus-induced B-cell immortalization. Genome Res 24:177-84
Prusevich, Polina; Kalin, Jay H; Ming, Shonoi A et al. (2014) A selective phenelzine analogue inhibitor of histone demethylase LSD1. ACS Chem Biol 9:1284-93
Feinberg, Andrew P (2013) A third-generation method reveals cell lineage ancestry. Nat Methods 10:117-8
Lennerz, Jochen K; Timmerman, Robert J; Grange, Dorothy K et al. (2010) Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield. J Mol Diagn 12:576-88
Mummert, Stephanie K; Lobanenkov, Victor A; Feinberg, Andrew P (2005) Association of chromosome arm 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor. Genes Chromosomes Cancer 43:155-61
Feinberg, A P (2005) A genetic approach to cancer epigenetics. Cold Spring Harb Symp Quant Biol 70:335-41
Wangler, Michael F; Chang, Aimee S; Moley, Kelle H et al. (2005) Factors associated with preterm delivery in mothers of children with Beckwith-Wiedemann syndrome: a case cohort study from the BWS registry. Am J Med Genet A 134A:187-91
Chang, Aimee S; Moley, Kelle H; Wangler, Michael et al. (2005) Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients. Fertil Steril 83:349-54
Niemitz, Emily L; DeBaun, Michael R; Fallon, Jonathan et al. (2004) Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome. Am J Hum Genet 75:844-9

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