Evidence map›Paper›PMID 41639146›Full record

ArticleScientific reports2026

Synergistic targeting of the ARID2-MYC axis by pomalidomide and panobinostat overcomes intrinsic IMiD resistance in multiple myeloma.

Junichi Yamamoto, Tomoko Asatsuma-Okumura, Takumi Ito, Yoshiko Iwai, Hiroshi Handa, Yuki Yamaguchi

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Junichi YamamotoSchool of Life Science and Technology, Institute of Science Tokyo, Yokohama, 226-8501, Japan. yamamoto.j.0c42@m.isct.ac.jp.
Tomoko Asatsuma-OkumuraDepartment of Cell Biology, Institute of Advanced Medical Sciences, Graduate School of Medicine, Nippon Medical School, Bunkyo, 113-8602, Japan.
Takumi ItoInstitute of Medical Science, Tokyo Medical University, Shinjuku, 160-8402, Japan.
Yoshiko IwaiDepartment of Cell Biology, Institute of Advanced Medical Sciences, Graduate School of Medicine, Nippon Medical School, Bunkyo, 113-8602, Japan.
Hiroshi HandaDepartment of Molecular Pharmacology, Center for Future Medical Research, Institute of Medical Science, Tokyo Medical University, Shinjuku, 160-8402, Japan.
Yuki YamaguchiSchool of Life Science and Technology, Institute of Science Tokyo, Yokohama, 226-8501, Japan.

Funding

Japan Society for the Promotion of Science 20K16314Japan Society for the Promotion of Science 23H04926Japan Society for the Promotion of Science 23K07807Japan Society for the Promotion of Science 24K02003
6 · The paper itself

Abstract

Multiple myeloma remains a therapeutic challenge despite recent advances with proteasome inhibitors, immunomodulatory drugs (IMiDs), and monoclonal antibodies. Among new approaches, the combination of IMiDs and histone deacetylase inhibitors has shown promise in relapsed or refractory multiple myeloma. Here, we elucidate the molecular basis of their synergy and its role in overcoming drug resistance in myeloma cells. We demonstrate that these agents converge to downregulate the master oncogene MYC, resulting in synergistic cytotoxicity. Importantly, this effect persists even in models intrinsically resistant to IMiDs, where the canonical IKZF1/3-IRF4/MYC axis is functionally uncoupled. In this context, the combination engages an alternative ARID2-MYC axis, mediated by the synergistic downregulation of the IMiD neosubstrate ARID2. This finding highlights the functional relevance of IMiD's inherent polypharmacology in circumventing primary resistance mechanisms at the cellular level. Together, our results identify the ARID2-containing PBAF complex as a critical vulnerability in resistant myeloma cells and provide a mechanistic rationale for designing combination strategies that co-target this complex, with the potential to enhance therapeutic efficacy by overcoming drug resistance.

Indexed as

Drug Resistance, NeoplasmHistone Deacetylase InhibitorsImmunologic FactorsMultiple MyelomaPanobinostatProto-Oncogene Proteins c-mycAdaptor Proteins, Signal TransducingAntineoplastic AgentsCell Line, TumorDrug Screening Assays, AntitumorDrug SynergismGenes, mycThalidomideTranscription FactorsUbiquitin-Protein LigasesAdaptor Proteins, Signal TransducingAntineoplastic AgentsARID2 protein, humanCRBN protein, humanHistone Deacetylase InhibitorsImmunologic FactorsMYC protein, humanPanobinostatpomalidomideProto-Oncogene Proteins c-mycThalidomideTranscription FactorsUbiquitin-Protein Ligases

Identifiers

PMID41639146
PMCPMC12923561

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.