Evidence map›Paper›PMID 17197433›Full record

ArticleBlood2007

Oridonin, a diterpenoid extracted from medicinal herbs, targets AML1-ETO fusion protein and shows potent antitumor activity with low adverse effects on t(8;21) leukemia in vitro and in vivo.

Guang-Biao Zhou, Hui Kang, Lan Wang, Li Gao, Ping Liu, Jun Xie, Feng-Xiang Zhang, Xiang-Qin Weng, Zhi-Xiang Shen, Jue Chen and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

101 citing papers in PubMed, 197 citations in OpenAlex.

  1. Efficacy of rabdosia rubescens in the treatment of gingivitis.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2009
    Trial
  2. Article
  3. Review
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  6. Review
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  8. Oridonin fromFood science & nutrition · 2024
    Review
  9. Synthetic Derivatives of NaturalInternational journal of molecular sciences · 2024
    Article
  10. Article
  11. Article
  12. Article
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  14. Article
  15. [Juglone induces proliferation inhibition and apoptosis of cervical cancer cellsNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
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  19. Article
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41 more citing papers are in PubMed but not listed here.

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

16 authors at 6 institutions in 2 countries.

Guang-Biao ZhouState Key Laboratory of Medical Genomics and Shanghai Institute of Hematology, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Shanghai 200025, China. zhou_guangbiao@gibh.org
Hui Kang
Lan Wang
Li Gao
Ping Liu
Jun Xie
Feng-Xiang Zhang
Xiang-Qin Weng
Zhi-Xiang Shen
Jue Chen
Long-Jun Gu
Ming Yan
Dong-Er Zhang
Sai-Juan Chen
Zhen-Yi Wang
Zhu Chen
Shanghai Jiao Tong University · CNShanghai Institute of Hematology · CNScripps Research Institute · USChinese Academy of Sciences · CNGuangzhou Institutes of Biomedicine and Health · CNShanghai Children's Medical Center · CN

Funding

T(8;21) in Blood Cell Proliferation and DifferentiationR01CA096735 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHANG, DONG-ER · 2003 to 2013
$3.4M
NCI NIH HHS CA 96735NCI NIH HHS R01 CA096735
6 · The paper itself

Abstract

Studies have documented the potential antitumor activities of oridonin, a compound extracted from medicinal herbs. However, whether oridonin can be used in the selected setting of hematology/oncology remains obscure. Here, we reported that oridonin induced apoptosis of t(8;21) acute myeloid leukemic (AML) cells. Intriguingly, the t(8;21) product AML1-ETO (AE) fusion protein, which plays a critical role in leukemogenesis, was degraded with generation of a catabolic fragment, while the expression pattern of AE target genes investigated could be reprogrammed. The ectopic expression of AE enhanced the apoptotic effect of oridonin in U937 cells. Preincubation with caspase inhibitors blocked oridonin-triggered cleavage of AE, while substitution of Ala for Asp at residues 188 in ETO moiety of the fusion abrogated AE degradation. Furthermore, oridonin prolonged lifespan of C57 mice bearing truncated AE-expressing leukemic cells without suppression of bone marrow or reduction of body weight of animals, and exerted synergic effects while combined with cytosine arabinoside. Oridonin also inhibited tumor growth in nude mice inoculated with t(8;21)-harboring Kasumi-1 cells. These results suggest that oridonin may be a potential antileukemia agent that targets AE oncoprotein at residue D188 with low adverse effect, and may be helpful for the treatment of patients with t(8;21) AML.

Indexed as

AnimalsAntineoplastic AgentsApoptosisChromosomes, Human, Pair 21Chromosomes, Human, Pair 8Core Binding Factor Alpha 2 SubunitCytarabineDiterpenesDiterpenes, KauraneDrug Screening Assays, AntitumorDrug SynergismHumansLeukemia, Myeloid, AcuteMiceMice, NudeNeoplasms, ExperimentalAML1-ETO fusion protein, humanAntineoplastic AgentsCore Binding Factor Alpha 2 SubunitCytarabineDiterpenesDiterpenes, KauraneOncogene Proteins, FusionoridoninPlant ExtractsRUNX1 Translocation Partner 1 Protein

Identifiers

PMID17197433
PMCPMC1852250
OpenAlexW2132055765

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.