Evidence map›Paper›PMID 33841673›Full record

ArticleAmerican journal of translational research2021

Anlotinib suppresses MLL-rearranged acute myeloid leukemia cell growth by inhibiting SETD1A/AKT-mediated DNA damage response.

Jinzhu Chen, Juan Feng, Zhihong Fang, Jing Ye, Qinwei Chen, Qiuling Chen, Kai Chen, Xiaoming Xiong, Guowei Li, Haihan Song and 1 more

Abstract read
In one paragraph

Article in American journal of translational research, 2021. 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. Review
  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

11 authors.

Jinzhu ChenDepartment of Hematology, The First Hospital of Longhai 363199 Fujian, P. R. China.
Juan FengDepartment of Hematology, The First Affiliated Hospital of Xiamen University and Institute of Hematology, School of Medicine, Xiamen University Xiamen 361003, P. R. China.
Zhihong FangDepartment of Hematology, The First Affiliated Hospital of Xiamen University and Institute of Hematology, School of Medicine, Xiamen University Xiamen 361003, P. R. China.
Jing YeDepartment of Hematology, The First Affiliated Hospital of Xiamen University and Institute of Hematology, School of Medicine, Xiamen University Xiamen 361003, P. R. China.
Qinwei ChenDepartment of Hematology, The First Affiliated Hospital of Xiamen University and Institute of Hematology, School of Medicine, Xiamen University Xiamen 361003, P. R. China.
Qiuling ChenDepartment of Hematology, The First Affiliated Hospital of Xiamen University and Institute of Hematology, School of Medicine, Xiamen University Xiamen 361003, P. R. China.
Kai ChenThe First People's Hospital of Foshan (The Affiliated Foshan Hospital of Sun Yat-sen University) Foshan 528000, Guangdong, P. R. China.
Xiaoming XiongDepartment of Hematology, The First Hospital of Longhai 363199 Fujian, P. R. China.
Guowei LiDepartment of Hematology, Huizhou Municipal Central Hospital Huizhou 516001, P. R. China.
Haihan SongDepartment of Immunology, DICAT Biomedical Computation Centre Vancouver, BC, Canada.
Bing XuDepartment of Hematology, The First Affiliated Hospital of Xiamen University and Institute of Hematology, School of Medicine, Xiamen University Xiamen 361003, P. R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leukemias driven by chromosomal translocation of the mixed-lineage leukemia (MLL) gene are highly prevalent in hematological malignancy. The poor survival rate and lack of effective targeted therapy for patients with MLL-rearranged (MLL-r) leukemias emphasize an urgent need for improved knowledge and novel therapeutic approaches for these malignancies. The present study aimed to investigate the potential effectiveness and mechanism of Anlotinib, a novel receptor tyrosine kinase inhibitor, in MLL-r acute myeloid leukemia (AML). The findings revealed that Anlotinib significantly inhibited the growth of MLL-r AML cells in both

Indexed as

AnlotinibDNA damageMLL-rearranged acute myeloid leukemiaSETD1A/AKT

Identifiers

PMID33841673
PMCPMC8014360

What OpenQuestion holds

Textmetadata
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.