Evidence map›Paper›PMID 21594647›Full record

ArticleMolecular and cellular biochemistry2011

Curcumin suppresses growth of mesothelioma cells in vitro and in vivo, in part, by stimulating apoptosis.

Ying Wang, Arun K Rishi, Wenjuan Wu, Lisa Polin, Sunita Sharma, Edi Levi, Steven Albelda, Harvey I Pass, Anil Wali

Abstract read
In one paragraph

Article in Molecular and cellular biochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Curcumin as an Anticancer Agent in Malignant Mesothelioma: A Review.International journal of molecular sciences · 2020
    Review
  6. Curcumin and Cancer.Nutrients · 2019
    Review
  7. Article
  8. Article
  9. Article
  10. Administering Fixed Oral Doses of Curcumin to Rats through Voluntary Consumption.Journal of the American Association for Laboratory Animal Science : JAALAS · 2018
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Curcumin: a double hit on malignant mesothelioma.Cancer prevention research (Philadelphia, Pa.) · 2014
    Article
  17. Article
  18. Article
  19. Review
  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

9 authors at 5 institutions in 1 country.

Ying WangJohn D. Dingell VA Medical Center, Karmanos Cancer Institute, Wayne State University, VAMC, 4646 John R, Detroit, MI 48201, USA.
Arun K Rishi
Wenjuan Wu
Lisa Polin
Sunita Sharma
Edi Levi
Steven Albelda
Harvey I Pass
Anil Wali
The Barbara Ann Karmanos Cancer Institute · USWayne State University · USJohn D. Dingell VA Medical Center · USNew York University · USUniversity of Pennsylvania · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Jennifer L Beebe-Dimmer · 1985 to 2026
$68.4M
NCI NIH HHS P30 CA022453
6 · The paper itself

Abstract

Malignant pleural mesothelioma (MPM) is an aggressive, asbestos-related malignancy of the thoracic pleura. Although, platinum-based agents are the first line of therapy, there is an urgent need for second-line therapies to treat the drug-resistant MPM. Cell cycle as well as apoptosis pathways are frequently altered in MPM and thus remain attractive targets for intervention strategies. Curcumin, the major component in the spice turmeric, alone or in combination with other chemotherapeutics has been under investigation for a number of cancers. In this study, we investigated the biological and molecular responses of MPM cells to curcumin treatments and the mechanisms involved. Flow-cytometric analyses coupled with western immunoblotting and gene-array analyses were conducted to determine mechanisms of curcumin-dependent growth suppression of human (H2373, H2452, H2461, and H226) and murine (AB12) MPM cells. Curcumin inhibited MPM cell growth in a dose- and time-dependent manner while pretreatment of MPM cells with curcumin enhanced cisplatin efficacy. Curcumin activated the stress-activated p38 kinase, caspases 9 and 3, caused elevated levels of proapoptotic proteins Bax, stimulated PARP cleavage, and apoptosis. In addition, curcumin treatments stimulated expression of novel transducers of cell growth suppression such as CARP-1, XAF1, and SULF1 proteins. Oral administration of curcumin inhibited growth of murine MPM cell-derived tumors in vivo in part by stimulating apoptosis. Thus, curcumin targets cell cycle and promotes apoptosis to suppress MPM growth in vitro and in vivo. Our studies provide a proof-of-principle rationale for further in-depth analysis of MPM growth suppression mechanisms and their future exploitation in effective management of resistant MPM.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAntineoplastic AgentsApoptosisApoptosis Regulatory Proteinsbcl-2-Associated X ProteinCarrier ProteinsCaspasesCell Cycle ProteinsCell Line, TumorCell ProliferationCurcuminDose-Response Relationship, DrugGene Expression RegulationHumansIntracellular Signaling Peptides and ProteinsAdaptor Proteins, Signal TransducingAntineoplastic AgentsApoptosis Regulatory Proteinsbcl-2-Associated X ProteinCarrier ProteinsCaspasesCCAR1 protein, humanCell Cycle ProteinsCurcuminIntracellular Signaling Peptides and ProteinsNeoplasm Proteinsp38 Mitogen-Activated Protein KinasesSULF1 protein, humanSulfotransferasesXAF1 protein, human

Identifiers

PMID21594647
PMCPMC3809898
OpenAlexW2038146198

What OpenQuestion holds

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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.