Evidence map›Paper›PMID 38442309›Full record

ArticleBlood cancer discovery2024

Acquired Multidrug Resistance in AML Is Caused by Low Apoptotic Priming in Relapsed Myeloblasts.

Elyse A Olesinski, Karanpreet Singh Bhatia, Chuqi Wang, Marissa S Pioso, Xiao Xian Lin, Ahmed M Mamdouh, Shu Xuan Ng, Vedant Sandhu, Shaista Shabbir Jasdanwala, Binyam Yilma and 13 more

Open access · greenAbstract read
In one paragraph

Article in Blood cancer discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 8% of its field
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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Pandora's Box of AML: HowBiomedicines · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
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

23 authors at 5 institutions in 4 countries.

Elyse A Olesinski *Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-2717-9755
Karanpreet Singh Bhatia *Department of Pharmacy, National University of Singapore, Singapore.ORCID 0009-0001-9004-1257
Chuqi WangDepartment of Pharmacy, National University of Singapore, Singapore.ORCID 0009-0004-8973-5595
Marissa S PiosoDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-2938-6678
Xiao Xian LinDepartment of Pharmacy, National University of Singapore, Singapore.ORCID 0009-0001-4226-9994
Ahmed M MamdouhDepartment of Pharmacy, National University of Singapore, Singapore.ORCID 0009-0005-3849-4389
Shu Xuan NgDepartment of Pharmacy, National University of Singapore, Singapore.ORCID 0009-0006-4193-6552
Vedant SandhuDepartment of Pharmacy, National University of Singapore, Singapore.ORCID 0009-0009-5114-8439
Shaista Shabbir JasdanwalaDepartment of Pharmacy, National University of Singapore, Singapore.ORCID 0009-0005-9391-362X
Binyam YilmaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0009-0007-8845-5390
Stephan BohlDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0001-9379-3342
Jeremy A RyanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-3327-1283
Disha MalaniDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0001-9614-3281
Marlise R LuskinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-5781-4529
Olli KallioniemiInstitute for Molecular Medicine Finland FIMM, Hi-Life, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-3231-0332
Kimmo PorkkaHematology Research Unit Helsinki, University of Helsinki and Helsinki University Hospital Comprehensive Cancer Center, Department of Hematology, HUS, Helsinki, Finland.ORCID 0000-0003-4112-5902
Sophia AdamiaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0001-5704-6040
Wee Joo ChngCancer Science Institute of Singapore, National University of Singapore, Centre for Translational Medicine, Singapore.ORCID 0000-0003-2578-8335
Motomi OsatoCancer Science Institute of Singapore, National University of Singapore, Centre for Translational Medicine, Singapore.ORCID 0000-0003-3982-9054
David M WeinstockDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-8724-3907
Jacqueline S GarciaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0003-2118-6302
Anthony LetaiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-1993-9013
Shruti BhattDepartment of Pharmacy, National University of Singapore, Singapore.ORCID 0000-0002-2617-5082
National University of Singapore · SGHarvard University · USDana-Farber Cancer Institute · USScience for Life Laboratory · SEUniversity of Helsinki · FI

Funding

TYROSINE KINASE ONCOGENESIS IN MYELOID LEUKEMIAP01CA066996 · NCI · DANA-FARBER CANCER INSTITUTE · PI SCOTT A ARMSTRONG · 1996 to 2026
$52.5M
Targeting SYK Kinase in AMLP50CA206963 · NCI · DANA-FARBER CANCER INST · PI STEGMAIER, KIMBERLY · 2017 to 2021
$10.6M
Reading mitochondrial apoptotic signaling to identify active cancer therapeuticsR35CA242427 · NCI · DANA-FARBER CANCER INST · PI LETAI, ANTHONY G · 2019 to 2025
$7.0M
Targeting High-Risk Lymphoid NeoplasmsR35CA231958 · NCI · DANA-FARBER CANCER INST · PI WEINSTOCK, DAVID MARC · 2019 to 2021
$2.9M
Enhancing Venetoclax Activity in Chemoresistant Acute Myeloid LeukemiaK08CA245209 · NCI · DANA-FARBER CANCER INST · PI GARCIA, JACQUELINE SUEN · 2020 to 2024
$1.3M
NCI NIH HHS K08 CA245209NCI NIH HHS P01 CA066996NCI NIH HHS P50 CA206963NCI NIH HHS R35 CA231958NCI NIH HHS R35 CA242427
6 · The paper itself

Abstract

In many cancers, mortality is associated with the emergence of relapse with multidrug resistance (MDR). Thus far, the investigation of cancer relapse mechanisms has largely focused on acquired genetic mutations. Using acute myeloid leukemia (AML) patient-derived xenografts (PDX), we systematically elucidated a basis of MDR and identified drug sensitivity in relapsed AML. We derived pharmacologic sensitivity for 22 AML PDX models using dynamic BH3 profiling (DBP), together with genomics and transcriptomics. Using in vivo acquired resistant PDXs, we found that resistance to unrelated, narrowly targeted agents in distinct PDXs was accompanied by broad resistance to drugs with disparate mechanisms. Moreover, baseline mitochondrial apoptotic priming was consistently reduced regardless of the class of drug-inducing selection. By applying DBP, we identified drugs showing effective in vivo activity in resistant models. This study implies evasion of apoptosis drives drug resistance and demonstrates the feasibility of the DBP approach to identify active drugs for patients with relapsed AML. SIGNIFICANCE: Acquired resistance to targeted therapy remains challenging in AML. We found that reduction in mitochondrial priming and common transcriptomic signatures was a conserved mechanism of acquired resistance across different drug classes in vivo. Drugs active in vivo can be identified even in the multidrug resistant state by DBP.

Indexed as

ApoptosisDrug Resistance, MultipleDrug Resistance, NeoplasmLeukemia, Myeloid, AcuteAnimalsAntineoplastic AgentsGranulocyte Precursor CellsHumansMiceXenograft Model Antitumor AssaysAntineoplastic Agents

Identifiers

PMID38442309
PMCPMC11061585
OpenAlexW4392447594

What OpenQuestion holds

Textmetadata
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.