Evidence map›Paper›PMID 27709797›Full record

ArticleCancer medicine2016

Homoharringtonine combined with aclarubicin and cytarabine synergistically induces apoptosis in t(8;21) leukemia cells and triggers caspase-3-mediated cleavage of the AML1-ETO oncoprotein.

Jiang Cao, Hao Feng, Ning-Ning Ding, Qing-Yun Wu, Chong Chen, Ming-Shan Niu, Wei Chen, Ting-Ting Qiu, Hong-Hu Zhu, Kai-Lin Xu

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. [How I treat acute myeloid leukemia with t (8;21)].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2017
    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

10 authors at 3 institutions in 1 country.

Jiang CaoDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College, XuZhou, 221002, China.
Hao FengDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College, XuZhou, 221002, China.
Ning-Ning DingDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College, XuZhou, 221002, China.
Qing-Yun WuDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College, XuZhou, 221002, China.
Chong ChenDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College, XuZhou, 221002, China.
Ming-Shan NiuDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College, XuZhou, 221002, China.
Wei ChenDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College, XuZhou, 221002, China.
Ting-Ting QiuDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College, XuZhou, 221002, China.
Hong-Hu ZhuDepartment of Hematology, Peking University People's Hospital, Beijing, 100044, China.
Kai-Lin XuDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical College, XuZhou, 221002, China.
Xuzhou Medical College · CNAffiliated Hospital of Xuzhou Medical College · CNPeking University People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homoharringtonine combined with aclarubicin and cytarabine (HAA) is a highly effective treatment for acute myeloid leukemia (AML), especially for t(8;21) AML. However, the underlying mechanisms by which HAA kills t(8;21) AML cells remain unclear. In this study, SKNO-1 and Kasumi-1 cells with t(8;21) were used. Compared with individual or pairwise administration of homoharringtonine, aclarubicin, or cytarabine, HAA showed the strongest inhibition of growth and induction of apoptosis in SKNO-1 and Kasumi-1 cells. HAA caused cleavage of the AML1-ETO (AE) oncoprotein to form truncated AE (ΔAE). Pretreatment with the caspase-3 inhibitor caspase-3 inhibitor Q-DEVD-OPh (QDO) not only suppressed HAA-induced apoptosis but also abrogated the cleavage of AE and generation of ΔAE. These results suggest that HAA synergistically induces apoptosis in t(8;21) leukemia cells and triggers caspase-3-mediated cleavage of the AML1-ETO oncoprotein, thus providing direct evidence for the strong activity of HAA toward t(8;21) AML.

Indexed as

Translocation, GeneticAclarubicinAntineoplastic AgentsApoptosisCaspase 3Cell Line, TumorCell ProliferationChromosomes, Human, Pair 21Chromosomes, Human, Pair 8Core Binding Factor Alpha 2 SubunitCytarabineDrug SynergismHarringtoninesHomoharringtonineHumansLeukemiaAclarubicinAML1-ETO fusion protein, humanAntineoplastic AgentsCaspase 3Core Binding Factor Alpha 2 SubunitCytarabineHarringtoninesHomoharringtonineOncogene Proteins, FusionRUNX1 Translocation Partner 1 ProteinAcute myeloid leukemiaAML1-ETOhomoharringtonine combined with aclarubicin and cytarabinesynergistic

Identifiers

PMID27709797
PMCPMC5119976
OpenAlexW2528032015

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.