Evidence map›Paper›PMID 34035227›Full record

ArticleCell death discovery2021

CD52 is a novel target for the treatment of FLT3-ITD-mutated myeloid leukemia.

Sivasundaram Karnan, Ichiro Hanamura, Akinobu Ota, Souichi Takasugi, Ayano Nakamura, Miyuki Takahashi, Kaori Uchino, Satsuki Murakami, Md Wahiduzzaman, Lam Quang Vu and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

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  8. Cytotoxicity ofMolecules (Basel, Switzerland) · 2022
    Article
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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 1 institution in 1 country.

Sivasundaram Karnan *Department of Biochemistry, Aichi Medical University, Nagakute, Aichi, Japan.
Ichiro Hanamura *Division of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute, Aichi, Japan. hanamura@aichi-med-u.ac.jp.
Akinobu OtaDepartment of Biochemistry, Aichi Medical University, Nagakute, Aichi, Japan.ORCID http://orcid.org/0000-0002-6296-2921
Souichi TakasugiDivision of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Ayano NakamuraDivision of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Miyuki TakahashiDivision of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Kaori UchinoDivision of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute, Aichi, Japan.ORCID http://orcid.org/0000-0003-2983-2129
Satsuki MurakamiDivision of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Md WahiduzzamanDepartment of Biochemistry, Aichi Medical University, Nagakute, Aichi, Japan.
Lam Quang VuDivision of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Md Lutfur RahmanDepartment of Biochemistry, Aichi Medical University, Nagakute, Aichi, Japan.
Muhammad Nazmul HasanDepartment of Biochemistry, Aichi Medical University, Nagakute, Aichi, Japan.ORCID http://orcid.org/0000-0003-2536-7557
Toshinori HyodoDepartment of Biochemistry, Aichi Medical University, Nagakute, Aichi, Japan.
Hiroyuki KonishiDepartment of Biochemistry, Aichi Medical University, Nagakute, Aichi, Japan.ORCID http://orcid.org/0000-0003-1131-4905
Shinobu TsuzukiDepartment of Biochemistry, Aichi Medical University, Nagakute, Aichi, Japan.
Kazuhiro YoshikawaResearch Creation Support Center, Aichi Medical University, Nagakute, Aichi, Japan.
Susumu SuzukiResearch Creation Support Center, Aichi Medical University, Nagakute, Aichi, Japan.
Ryuzo UedaDepartment of Tumor Immunology, Aichi Medical University, Nagakute, Aichi, Japan.
Masayuki EjiriDepartment of Pharmacy, Aichi Medical University, Nagakute, Aichi, Japan.
Yoshitaka HosokawaDepartment of Biochemistry, Aichi Medical University, Nagakute, Aichi, Japan.
Akiyoshi TakamiDivision of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute, Aichi, Japan.ORCID http://orcid.org/0000-0002-1822-9976
Aichi Medical University · JP

Funding

Ministry of Education, Culture, Sports, Science and Technology (MEXT) 18K07277Ministry of Education, Culture, Sports, Science and Technology (MEXT) 18K08342Ministry of Education, Culture, Sports, Science and Technology (MEXT) 19K08825Ministry of Education, Culture, Sports, Science and Technology (MEXT) 19K09292
6 · The paper itself

Abstract

Internal tandem duplication (ITD) of FMS-like tyrosine kinase 3 (FLT3) confers poor prognosis and is found in approximately 25% of cases of acute myeloid leukemia (AML). Although FLT3 inhibitors have shown clinical benefit in patients with AML harboring FLT3-ITD, the therapeutic effect is limited. Here, to explore alternative therapeutics, we established a cellular model of monoallelic FLT3

Identifiers

PMID34035227
PMCPMC8149417
OpenAlexW3165268477

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.