Evidence map›Paper›PMID 39383379›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2024

Synergistic effect of venetoclax and ibrutinib on ibrutinib-resistant ABC-type DLBCL cells.

Fengbo Jin, Limei He, Yingying Chen, Wanlu Tian, Lixia Liu, Ling Ge, Wei Qian, Leiming Xia, Mingzhen Yang

Abstract read
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2024. 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

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

9 authors.

Fengbo JinDepartment of Hematopathology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.ORCID http://orcid.org/0000-0001-6545-9400
Limei HeDepartment of Hematopathology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.ORCID http://orcid.org/0009-0001-5781-000X
Yingying ChenDepartment of Hematopathology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.ORCID http://orcid.org/0009-0000-5583-6241
Wanlu TianDepartment of Hematopathology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.ORCID http://orcid.org/0009-0003-4539-9107
Lixia LiuDepartment of Hematopathology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.ORCID http://orcid.org/0009-0008-8588-1383
Ling GeDepartment of Hematopathology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.ORCID http://orcid.org/0009-0004-2556-693X
Wei QianDepartment of Hematopathology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.ORCID http://orcid.org/0009-0009-4216-1949
Leiming XiaDepartment of Hematopathology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.ORCID http://orcid.org/0000-0002-6760-0153
Mingzhen YangDepartment of Hematopathology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.ORCID http://orcid.org/0000-0002-9667-1583

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the widespread use of R-CHOP therapy in diffuse large B-cell lymphoma (DLBCL), the therapeutic efficacy for this disease remains suboptimal, primarily due to the heterogeneity of refractory and/or relapsed diseases. To address this challenge, optimization of DLBCL treatment regimens has focused on the strategy of combining an additional drug "X" with R-CHOP to enhance efficacy. However, the failure of R-CHOP combined with the BTK inhibitor ibrutinib in treating ABC-type DLBCL patients has raised significant concerns regarding ibrutinib resistance. While some studies suggest that venetoclax may synergize with ibrutinib to kill ibrutinib-resistant cells, the underlying mechanisms remain unclear. Our study aimed to validate the enhanced tumor-suppressive effect of combining ibrutinib with venetoclax against ibrutinib-resistant cells and elucidate its potential mechanisms. Our experimental results demonstrated that ibrutinib-resistant cells exhibited significant cytotoxicity to the combination therapy of ibrutinib and venetoclax, inducing cell apoptosis through activation of the mitochondrial pathway and inhibition of aerobic respiration. Furthermore, we validated the inhibitory effect of this combination therapy on tumor growth in in vivo models. Therefore, our study proposes that the combination therapy of ibrutinib and venetoclax is a promising treatment strategy that can be applied in clinical practice for ABC-type DLBCL, offering a new solution to overcome the urgent challenge of ibrutinib resistance.

Indexed as

AdenineApoptosisBridged Bicyclo Compounds, HeterocyclicDrug Resistance, NeoplasmDrug SynergismLymphoma, Large B-Cell, DiffusePiperidinesPyrazolesPyrimidinesSulfonamidesAnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsCell Line, TumorHumansMiceAdenineAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicibrutinibPiperidinesPyrazolesPyrimidinesSulfonamidesvenetoclax

Identifiers

PMID39383379
PMCPMC11463907

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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.