Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (H3K27ac Cut&Tag)

ABSTRACT: Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (H3K27ac Cut&Tag)

PROVIDER: PRJNA1003429 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Similar Datasets

Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming [CUT&Tag]

Project description:Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming [CUT&Tag]

| PRJNA1260415 | ENA

Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming

Project description:Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming

| PRJNA1003417 | ENA

Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (CRISPR)

Project description:Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (CRISPR)

| PRJNA1005615 | ENA

Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (H3K27ac Cut&Tag)

Project description:Metabolites are essential substrates for epigenetic modifications. Although nuclear acetyl-CoA constitutes a small fraction of the whole cell pool, it regulates cell fate by locally providing histone acetylation substrate. Here, we report a nucleus-specific acetyl-CoA regulatory mechanism that can be modulated to achieve therapeutic cancer cell reprogramming. Combining phenotypic chemical screen, genome-wide CRISPR screen, and proteomics, we identified that the nucleus-localized pyruvate dehydrogenase complex (nPDC) is constitutively inhibited by the nuclear protein ELMSAN1 through direct interaction. Pharmacologic inhibition of the ELMSAN1-nPDC interaction derepressed nPDC activity, enhancing nuclear acetyl-CoA generation and reprograming cancer cells to a postmitotic state with diminished cell-of-origin signatures. Reprogramming was synergistically enhanced by histone deacetylase 1/2 inhibition, resulting in inhibited tumor growth, durably suppressed tumor-initiating ability, and improved survival in multiple cancer types in vivo, including therapy-resistant sarcoma patient-derived xenografts and carcinoma cell line xenografts. Our findings highlight the potential of targeting ELMSAN1-nPDC as epigenetic cancer therapy.

2025-05-09 | GSE240353 | GEO

Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming [ATAC-Seq]

Project description:Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming [ATAC-Seq]

| PRJNA1260417 | ENA

Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (ATAC-seq)

Project description:Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (ATAC-seq)

| PRJNA1003428 | ENA

Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (RNA-seq_1)

Project description:Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (RNA-seq_1)

| PRJNA1003427 | ENA

Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (RNA-seq_2)

Project description:Derepressing nuclear pyruvate dehydrogenase induces therapeutic cancer cell reprogramming (RNA-seq_2)