Evidence map›Paper›PMID 40204951›Full record

ArticleCell death and differentiation2025

Re-appraising assays on permeabilized blood cancer cells testing venetoclax or other BH3 mimetic agents selectively targeting pro-survival BCL2 proteins.

Jia-Nan Gong, Tirta M Djajawi, Donia M Moujalled, Giovanna Pomilio, Tiffany Khong, Li-Ping Zhang, Pasquale L Fedele, Michael S Low, Mary Ann Anderson, Christopher D Riffkin and 11 more

Abstract read
In one paragraph

Article in Cell death and differentiation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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.

Jia-Nan GongWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia. gongjianan@cnilas.org.ORCID 0000-0003-4977-9775
Tirta M DjajawiWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Donia M MoujalledWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID 0000-0002-1076-3496
Giovanna PomilioWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Tiffany KhongAustralian Centre for Blood Diseases, Alfred Health-Monash University, Melbourne, VIC, Australia.
Li-Ping ZhangNHC Key Laboratory of Human Disease Comparative Medicine, The Institute of Laboratory Animal Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, National Human Diseases Animal Model Resource Center, National Center of Technology Innovation for Animal Model, Beijing, China.
Pasquale L FedeleWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Michael S LowWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Mary Ann AndersonWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Christopher D RiffkinWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Christine A WhiteWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID 0000-0001-8033-9140
Ping LanWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Guillaume LesseneWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID 0000-0002-1193-8147
Marco J HeroldWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID 0000-0001-7539-7581
Andreas StrasserWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID 0000-0002-5020-4891
Andrew SpencerAustralian Centre for Blood Diseases, Alfred Health-Monash University, Melbourne, VIC, Australia.
George GrigoriadisSchool of Clinical Sciences at Monash Health, Monash University, Clayton, VIC, Australia.
Andrew H WeiWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Mark F van DelftWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID 0000-0002-3866-4318
Andrew W RobertsWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia. roberts@wehi.edu.au.ORCID 0000-0002-7341-5720
David C S HuangWalter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia. huang_d@wehi.edu.au.ORCID 0000-0002-3101-4873

Funding

Department of Health | National Health and Medical Research Council (NHMRC) 1016701Department of Health | National Health and Medical Research Council (NHMRC) 1043149Department of Health | National Health and Medical Research Council (NHMRC) 1113133Leukemia and Lymphoma Society (Leukemia & Lymphoma Society) 7001-013Leukemia and Lymphoma Society (Leukemia & Lymphoma Society) 7015-18
6 · The paper itself

Abstract

BH3 mimetic drugs that selectively target the pro-survival BCL2 proteins are highly promising for cancer treatment, most notably for treating blood cancers. Venetoclax, which inhibits BCL2, is now approved for treating chronic lymphocytic leukemia (CLL) and acute myeloid leukemia (AML). Preferably, robust and validated assays would identify patients most likely to benefit from therapy with venetoclax itself or with inhibitors of other pro-survival proteins. A sophisticated method that has been developed is the BH3 profiling assay. In this assay, permeabilized, instead of intact, cells are treated for a few hours with inhibitors of the pro-survival BCL2 proteins, and the resultant mitochondrial depolarization measured. Sensitivity to a specific inhibitor (e.g., venetoclax or other BH3 mimetics) is then used to infer the reliance of a tumor (e.g., CLL) on one or more pro-survival BCL2 proteins. However, we found that this methodology cannot reliably identify such dependencies. In part, this is because almost all cells express multiple pro-survival BCL2 proteins that restrain BAX and BAK which must be inhibited before mitochondrial depolarization and apoptosis can proceed. Using genetic and pharmacological tools across multiple cell line models of blood cancer, we demonstrated that selective BCL2 inhibitors have important flow-on effects that includes the redistribution of BH3-only proteins to ancillary pro-survival proteins not directly engaged by the inhibitor. These secondary effects, critical to the biological action of selective inhibitors, were not accurately recapitulated in permeabilized cells, probably due to the limited time frame possible in such assays or the altered biophysical conditions when cells are permeabilized. While we could consistently define the sensitivity of a tumor cell to a particular BH3 mimetic drugs using intact cells, this was not reliable with permeabilized cells. These studies emphasize the need to carefully evaluate assays on permeabilized cells undertaken with inhibitors of the pro-survival BCL2 proteins.

Indexed as

Antineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicProto-Oncogene Proteins c-bcl-2SulfonamidesApoptosisbcl-2-Associated X ProteinCell Line, TumorCell SurvivalHumansAntineoplastic Agentsbcl-2-Associated X ProteinBCL2 protein, humanBridged Bicyclo Compounds, HeterocyclicProto-Oncogene Proteins c-bcl-2Sulfonamidesvenetoclax

Identifiers

PMID40204951
PMCPMC12325916

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Registered trials

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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.