Evidence map›Paper›PMID 38232702›Full record

ArticleCell reports. Medicine2024

Mapping the proteogenomic landscape enables prediction of drug response in acute myeloid leukemia.

James C Pino, Camilo Posso, Sunil K Joshi, Michael Nestor, Jamie Moon, Joshua R Hansen, Chelsea Hutchinson-Bunch, Marina A Gritsenko, Karl K Weitz, Kevin Watanabe-Smith and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. A Network-Driven Framework for Drug Response Precision Prediction of Acute Myeloid Leukemia.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. 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

21 authors at 2 institutions in 1 country.

James C PinoEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Camilo PossoEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Sunil K JoshiKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Division of Hematology & Medical Oncology, Department of Medicine, Oregon Health & Science University, Portland, OR, USA.
Michael NestorEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Jamie MoonEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Joshua R HansenEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Chelsea Hutchinson-BunchEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Marina A GritsenkoEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Karl K WeitzEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Kevin Watanabe-SmithDivision of Oncological Sciences, Oregon Health & Science University, Portland, OR, USA.
Nicola LongDivision of Oncological Sciences, Oregon Health & Science University, Portland, OR, USA.
Jason E McDermottEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA; Department of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, OR, USA.
Brian J DrukerKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Division of Hematology & Medical Oncology, Department of Medicine, Oregon Health & Science University, Portland, OR, USA; Division of Oncological Sciences, Oregon Health & Science University, Portland, OR, USA.
Tao LiuEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Jeffrey W TynerKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Division of Hematology & Medical Oncology, Department of Medicine, Oregon Health & Science University, Portland, OR, USA; Department of Cell, Developmental, and Cancer Biology, Oregon Health & Science University, Portland, OR, USA.
Anupriya AgarwalKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Division of Hematology & Medical Oncology, Department of Medicine, Oregon Health & Science University, Portland, OR, USA; Division of Oncological Sciences, Oregon Health & Science University, Portland, OR, USA; Department of Cell, Developmental, and Cancer Biology, Oregon Health & Science University, Portland, OR, USA.
Elie TraerKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Division of Hematology & Medical Oncology, Department of Medicine, Oregon Health & Science University, Portland, OR, USA.
Paul D PiehowskiEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Cristina E TognonKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA; Division of Hematology & Medical Oncology, Department of Medicine, Oregon Health & Science University, Portland, OR, USA.
Karin D RodlandEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA; Department of Cell, Developmental, and Cancer Biology, Oregon Health & Science University, Portland, OR, USA. Electronic address: rodland@ohsu.edu.
Sara J C GoslineEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA. Electronic address: sara.gosline@pnnl.gov.
Pacific Northwest National Laboratory · USOregon Health & Science University · US

Funding

Tumor Intrinsic and Microenvironmental Mechanisms Driving Drug Combination Efficacy and Resistance in AMLU54CA224019 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Tothu Q Vu · 2017 to 2026
$13.9M
Center for Advanced Multi-Omic Characterization of CancerU24CA271012 · NCI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI Tao Liu · 2022 to 2026
$6.6M
Proteogenomic characterization of early and late resistance mechanisms in acute myeloid leukemiaU01CA271412 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI BRIAN J DRUKER, Paul D Piehowski · 2022 to 2026
$5.8M
PNNL Proteome Characterization CenterU24CA210955 · NCI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI LIU, TAO, SMITH, RICHARD D · 2016 to 2020
$5.3M
Inflammation-Driven Clonal Evolution in RUNX1 Carriers: Mechanisms and Therapeutic VulnerabilitiesR01HL155426 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Anupriya Agarwal · 2021 to 2026
$2.7M
Studying drug resistance in AML and PDAC using a novel heterotypic 3D organoid modelR01CA229875 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI AGARWAL, ANUPRIYA · 2019 to 2023
$1.6M
Defining the stromal landscape that sustains AML drug resistanceF30CA239335 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JOSHI, SUNIL KUMAR · 2019 to 2022
$187k
NCI NIH HHS F30 CA239335NCI NIH HHS R01 CA229875NCI NIH HHS U01 CA271412NHLBI NIH HHS R01 HL155426
6 · The paper itself

Abstract

Acute myeloid leukemia is a poor-prognosis cancer commonly stratified by genetic aberrations, but these mutations are often heterogeneous and fail to consistently predict therapeutic response. Here, we combine transcriptomic, proteomic, and phosphoproteomic datasets with ex vivo drug sensitivity data to help understand the underlying pathophysiology of AML beyond mutations. We measure the proteome and phosphoproteome of 210 patients and combine them with genomic and transcriptomic measurements to identify four proteogenomic subtypes that complement existing genetic subtypes. We build a predictor to classify samples into subtypes and map them to a "landscape" that identifies specific drug response patterns. We then build a drug response prediction model to identify drugs that target distinct subtypes and validate our findings on cell lines representing various stages of quizartinib resistance. Our results show how multiomics data together with drug sensitivity data can inform therapy stratification and drug combinations in AML.

Indexed as

Leukemia, Myeloid, AcuteProteogenomicsGenomicsHumansMutationProteomicsacute myeloid leukemiadrug responsegenomicslinear regressionmultiomicsnon-negative matrix factorizationproteomicstranscriptomics

Identifiers

PMID38232702
PMCPMC10829797
OpenAlexW4390921274

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.