Evidence map›Paper›PMID 41106207›Full record

ArticleDrug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy2026

Combined HDAC and eIF4A inhibition: A novel epigenetic therapy for pancreatic ductal adenocarcinoma.

Maryam Safari, Luigi Scotto, Agnes Basseville, Thomas Litman, Haoran Xue, Lubov Petrukhin, Ping Zhou, Helen E Remotti, Amy Ku, Diana V Morales and 9 more

Abstract read
In one paragraph

Article in Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Maryam SafariDepartment of Medicine, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, NY, USA; Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA.
Luigi ScottoDepartment of Medicine, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, NY, USA.
Agnes BassevilleOmics Data Science Unit, Institut de Cancérologie de l'Ouest; F-, Angers 49055, France.
Thomas LitmanUniversity of Copenhagen, Copenhagen, Denmark.
Haoran XueDepartment of Chemistry and Biochemistry & The Baylor Synthesis and Drug-Lead Discovery Lab, Baylor University, Waco, TX, USA.
Lubov PetrukhinJames J Peters VA Medical Center; New York, NY, USA.
Ping ZhouJames J Peters VA Medical Center; New York, NY, USA.
Helen E RemottiDepartment of Pathology, Columbia University Irving Medical Center, New York, NY, USA.
Amy KuDepartment of Pathology, Columbia University Irving Medical Center, New York, NY, USA.
Diana V MoralesHerbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA.
Christopher DamociHerbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA.
Mingzhao ZhuDepartment of Chemistry and Biochemistry & The Baylor Synthesis and Drug-Lead Discovery Lab, Baylor University, Waco, TX, USA.
Ravikanth MaddipatiDepartment of Internal Medicine and Children's Research Institute, UT Southwestern Medical Center, Dallas, TX, USA.
Kenneth G HullDepartment of Chemistry and Biochemistry & The Baylor Synthesis and Drug-Lead Discovery Lab, Baylor University, Waco, TX, USA.
Robert W RobeyCenter for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Kenneth P OliveDepartment of Medicine, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, NY, USA; Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA.
Tito FojoDepartment of Medicine, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, NY, USA; James J Peters VA Medical Center; New York, NY, USA; Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA.
Daniel RomoDepartment of Chemistry and Biochemistry & The Baylor Synthesis and Drug-Lead Discovery Lab, Baylor University, Waco, TX, USA.
Susan E BatesDepartment of Medicine, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, NY, USA; James J Peters VA Medical Center; New York, NY, USA; Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA. Electronic address: seb2227@cumc.columbia.edu.

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
Pharmacophore-Directed  Retrosynthesis Applied to Bioactive Natural Products Informing Mechanism of Action StudiesR35GM134910 · NIGMS · BAYLOR UNIVERSITY · PI DANIEL ROMO · 2020 to 2026
$2.7M
Optogenetic engineering of tumor topography in native tissue environmentsDP2CA290967 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Ravikanth Maddipati · 2023 to 2026
$2.4M
NCI NIH HHS DP2 CA290967NCI NIH HHS P30 CA013696NIGMS NIH HHS R35 GM134910
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive and lethal malignancy. Emerging evidence suggests that epigenetic therapies have the potential to target key mechanisms driving PDAC progression and therapy resistance. Previous efforts to target KRAS-driven metabolic vulnerabilities, including dependence on enhanced fatty acid synthesis, have highlighted the potential for histone deacetylase (HDAC) inhibitors to deplete acetyl-CoA and induce DNA damage through histone acetylation, while resistance emerges at least in part due to the reversible nature of HDAC inhibitor-induced acetylation. In this work, we discovered that the combination of class I histone deacetylase (HDAC) inhibitors, such as romidepsin, with a novel RNA helicase eIF4A inhibitor, des-methyl pateamine A (DMPatA), induces robust and persistent hyperacetylation, significantly exceeding the levels and duration observed with HDAC inhibitor monotherapy. This combination synergistically reduces the viability of PDAC cells, even at low, nontoxic doses for both drugs. This unexpected synergistic effect triggers a cascade of cellular responses, including hypertranscription, metabolic stress, and augmented DNA damage. Sustained hyperacetylation represents a novel mechanism exploiting PDAC-specific vulnerabilities, simultaneously amplifying DNA damage and depleting acetyl-CoA levels critical for their aberrant proliferation. In vivo, the combination effectively suppresses tumor growth, showing no toxicity to normal tissues but sustained hyperacetylation in tumor tissue. The combination does not appear to induce known resistance mechanisms such as drug efflux; elevated MYC expression, rather than inducing resistance, sensitizes PDAC cells to treatment. These studies support translation of this synergistic combination to the clinic.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalDepsipeptidesEukaryotic Initiation Factor-4AHistone Deacetylase InhibitorsPancreatic NeoplasmsAcetylationAnimalsCell Line, TumorDNA DamageDrug SynergismEpigenesis, GeneticHumansMiceXenograft Model Antitumor AssaysDepsipeptidesEukaryotic Initiation Factor-4AHistone Deacetylase InhibitorsromidepsinAcetylationEIF4A InhibitorEpigenetic TherapyHDAC InhibitorPancreatic Cancer

Identifiers

PMID41106207
PMCPMC13322276

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.