Evidence map›Paper›PMID 22389266›Full record

ArticleMolecular carcinogenesis2013

Bioactive tanshinone I inhibits the growth of lung cancer in part via downregulation of Aurora A function.

Yanli Li, Yi Gong, Linglin Li, Hamid M Abdolmaleky, Jin-Rong Zhou

Abstract read
In one paragraph

Article in Molecular carcinogenesis, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
16.6field-weighted citation impact, top 1% 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

27 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. miR-137: a potential therapeutic target for lung cancer.Frontiers in cell and developmental biology · 2024
    Review
  5. Review
  6. Review
  7. Experimental and therapeutic medicine · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Modulation of GOncology letters · 2018
    Article
  20. 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

5 authors at 2 institutions in 2 countries.

Yanli LiInstitute of Molecular & Experimental Therapeutics, East China Normal University, Shanghai, China.
Yi Gong
Linglin Li
Hamid M Abdolmaleky
Jin-Rong Zhou
Beth Israel Deaconess Medical Center · USEast China Normal University · CN

Funding

Metabolic Syndrome as Pancreatic Cancer EtiologyR21CA127794 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ZHOU, JIN-RONG · 2008 to 2009
$421k
Targeting prostate cancer stem cells to delay prostate cancer progressionR21CA153355 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ZHOU, JIN-RONG · 2011 to 2012
$416k
Oldenlandia diffusa for prostate cancer treatmentR21CA133865 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ZHOU, JIN-RONG · 2007 to 2008
$374k
NCI NIH HHS CA133865NCI NIH HHS R21 CA127794NCI NIH HHS R21 CA133865NCI NIH HHS R21 CA153355
6 · The paper itself

Abstract

Lung cancer is the leading cause of cancer death in the world, and the searching for novel efficacious and safe agents for lung cancer prevention remains the top priority of lung cancer research. In the present study, we evaluated the effect of bioactive tanshinones from a Chinese herb Salvia miltiorrhiza, cryptotanshinone (CT), tanshinone I (T1) and tanshinone IIA (T2A), on the proliferation inhibition of lung cancer cell lines. Tanshinones inhibited the lung cancer cell proliferation in vitro, with T1 the most potent, via cell cycle arrest and apoptosis induction. Gene function assay showed that Aurora A knockdown by siRNA dramatically eliminated the T1 activity in vitro, suggesting that Aurora A is an important functional target for T1. We further evaluated the effectiveness of T1 on the growth of H1299 nonsmall lung cancer cell in a mouse model. Tanshinone I inhibited the growth of H1299 lung tumor in a dose-dependent manner. Tanshinone I at 200 mg/kg body weight significantly reduced final tumor weight by 34% (P < 0.05) associated with inhibiting proliferation and inducing apoptosis of lung cancer cells by 54% (P < 0.001) and 193% (P < 0.001), respectively, inhibiting lung tumor angiogenesis by 72% (P < 0.001), and reducing Aurora A expression by 67% (P < 0.001). On the other hand, T1 did not significantly alter food intake or body weight. Our results provided experimental evidence to suggest that T1 may be an efficacious and safe agent for the prevention of lung cancer progression and Aurora A may be an important molecular target for T1 action against lung cancer.

Indexed as

AbietanesAnimalsAntineoplastic Agents, PhytogenicApoptosisAurora Kinase AAurora KinasesBlotting, WesternBody WeightCarcinoma, Lewis LungCarcinoma, Non-Small-Cell LungCell AdhesionCell CycleCell MovementCell ProliferationFemaleHumansAbietanesAntineoplastic Agents, PhytogenicAurka protein, mouseAurora Kinase AAurora KinasesProtein Serine-Threonine KinasesRNA, Small Interferingtanshinone

Identifiers

PMID22389266
PMCPMC3376178
OpenAlexW2045261772

What OpenQuestion holds

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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.