Evidence map›Paper›PMID 36053810›Full record

ArticleMolecular oncology2022

Apatinib enhances chemosensitivity of ABT-199 in diffuse large B-cell lymphoma.

Yuanfei Shi, Jing Ye, Huafei Shen, Yi Xu, Rui Wan, Xiujin Ye, Jie Jin, Wanzhuo Xie

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2022. 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
0.6field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Caryophyllene Oxide, a Bicyclic Terpenoid Isolated fromInternational journal of molecular sciences · 2024
    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

8 authors at 3 institutions in 1 country.

Yuanfei ShiDepartment of Hematology, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Jing YeSports Medicine Department, Beijing Key Laboratory of Sports Injuries, Peking University Third Hospital, Beijing, China.
Huafei ShenDepartment of Hematology, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Yi XuDepartment of Hematology, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Rui WanDepartment of Intensive Care Unit, Taihe Hospital, Hubei University of Medicine, Shiyan, China.
Xiujin YeDepartment of Hematology, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Jie JinDepartment of Hematology, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Wanzhuo XieDepartment of Hematology, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.ORCID 0000-0002-0863-1814
First Affiliated Hospital Zhejiang University · CNHubei University of Medicine · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the effect of Apatinib (an inhibitor targeting VEGFR-2) enhances chemosensitivity of ABT-199 on diffuse large B-cell lymphoma (DLBCL). Viability assay and flow cytometric assay for determining apoptosis, cell cycle, mitochondrial membrane potential, reactive oxygen species and immunoblotting were used to explore the combination effect in DLBCL cell lines, DLBCL patient samples, and DLBCL mouse models. RNA sequencing assay helped identify mechanisms of ABT-199 plus Apatinib. The results show that ABT-199 combined with Apatinib inhibited cell proliferation, reduced colony-forming capacity, and induced apoptosis and cell cycle arrest in DLBCL cells. Mechanistically, the combination therapy inhibited tumour cell growth and promoted tumour cell death by regulating EDN1 and MAPK-related pathways and activating the intrinsic apoptotic pathway. The effect of the combination therapy was also validated in primary DLBCL blasts and xenograft mouse models. Our findings indicate that Apatinib enhances the chemosensitivity of ABT-199 and might serve as a promising therapeutic strategy for DLBCL.

Indexed as

Lymphoma, Large B-Cell, DiffuseVascular Endothelial Growth Factor Receptor-2AnimalsApoptosisBridged Bicyclo Compounds, HeterocyclicCell Line, TumorCell ProliferationHumansMicePyridinesReactive Oxygen SpeciesSulfonamidesXenograft Model Antitumor AssaysapatinibBridged Bicyclo Compounds, HeterocyclicPyridinesReactive Oxygen SpeciesSulfonamidesVascular Endothelial Growth Factor Receptor-2venetoclaxABT-199ApatinibDLBCLEDN1MAPKVEGFR-2

Identifiers

PMID36053810
PMCPMC9580892
OpenAlexW4293387989

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.