Evidence map›Paper›PMID 42608470›Full record

ArticleOncogene2026

The Inv(16) Oncogene CBFB::MYH11 is Required for the Survival of Leukemia Cells in the Blood and Spleen, but not the Bone Marrow.

Sipra Panda, Yiqian Wang, Venkatasai Rahul Dogiparthi, Michelle Becker, Arjun Dhir, Calvin Lam, Cecilia Rivas, Lemlem Alemu, Lisa Garrett, Peng Xiao and 3 more

Abstract read
In one paragraph

Article in Oncogene, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Sipra PandaDepartment of Biochemistry and Molecular Biology, Omaha, NE, USA.ORCID http://orcid.org/0000-0001-7145-6273
Yiqian WangDepartment of Biochemistry and Molecular Biology, Omaha, NE, USA.
Venkatasai Rahul DogiparthiFred and Pamela Buffett Cancer Center, Omaha, NE, USA.
Michelle BeckerDepartment of Biochemistry and Molecular Biology, Omaha, NE, USA.
Arjun DhirDepartment of Biochemistry and Molecular Biology, Omaha, NE, USA.
Calvin LamDepartment of Biochemistry and Molecular Biology, Omaha, NE, USA.
Cecilia RivasTransgenic Mouse Core, Bethesda, MD, USA.
Lemlem AlemuTranslational and Functional Genomics Branch, National Human Genome Research Institute, NIH, Bethesda, MD, USA.
Lisa GarrettTransgenic Mouse Core, Bethesda, MD, USA.
Peng XiaoDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
Samantha A SwensonDepartment of Biochemistry and Molecular Biology, Omaha, NE, USA.ORCID http://orcid.org/0000-0002-5650-3841
Kyle J HewittFred and Pamela Buffett Cancer Center, Omaha, NE, USA.
R Katherine HydeDepartment of Biochemistry and Molecular Biology, Omaha, NE, USA. kate.hyde@unmc.edu.ORCID http://orcid.org/0000-0003-2808-1749

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI James Eudy · 1985 to 2026
$55.0M
Target Validation CoreP20GM121316 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ADRIAN R BLACK · 2018 to 2026
$23.5M
The Role of the CBFB-MYH11 Complex in Leukemia MaintenanceR01CA244900 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HYDE, RICIA KATHERINE · 2020 to 2024
$1.9M
TRAINING PROGRAM IN VIRAL ONCOLOGYT32CA009467 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HUNTER, ERIC · 1985 to 2002
$691k
NCI NIH HHS P30 CA036727NCI NIH HHS R01 CA244900NCI NIH HHS T32 CA009467NIGMS NIH HHS P20 GM121316U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P30 CA036727U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01 CA244900U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) T32 CA009467U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) P20 GM121316
6 · The paper itself

Abstract

Inversion of chromosome 16 [inv(16)] generates the fusion gene CBFB::MYH11 (CM) and is one of the most common chromosomal rearrangements in Acute Myeloid Leukemia (AML). Expression of CM is required for leukemia initiation. Patients with inv(16) at diagnosis invariably have the rearrangement at relapse, leading to the assumption that CM is also required after leukemic transformation. However, a role for CM in leukemia maintenance has yet to be shown experimentally. To address this, we used an inducible CM knockdown (KD) mouse model and found that decreased CM eliminated leukemia cells from the peripheral blood and spleen, but not the bone marrow, despite all populations exhibiting significantly decreased CM mRNA and protein. The surviving CM KD cells in the bone marrow showed decreased apoptosis and proliferation, and increased expression of autophagy related genes. Surprisingly, with prolonged KD of CM, ~40% of mice re-established disease despite maintaining decreased CM. Our work indicates that CM is required for leukemia survival in the spleen and peripheral blood, but in the bone marrow CM KD leukemia cells can survive and re-establish disease independent of the fusion protein. These findings imply that targeting CM alone has potential to reduce leukemic burden but not cure the disease.

Indexed as

Bone MarrowChromosome InversionChromosomes, Human, Pair 16Core Binding Factor beta SubunitLeukemia, Myeloid, AcuteOncogene Proteins, FusionSpleenAnimalsApoptosisCell ProliferationCell SurvivalHumansMiceCBFbeta-MYH11 fusion proteinCore Binding Factor beta SubunitOncogene Proteins, Fusion

Identifiers

PMID42608470
PMCPMC13600926

What OpenQuestion holds

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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.