Evidence map›Paper›PMID 26075279›Full record

ArticleBioMed research international2015

Curcumin and its analogue induce apoptosis in leukemia cells and have additive effects with bortezomib in cellular and xenograft models.

L I Nagy, L Z Fehér, G J Szebeni, M Gyuris, P Sipos, R Alföldi, B Ózsvári, L Hackler, A Balázs, P Batár and 2 more

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Curcumin in treatment of hematological cancers: Promises and challenges.Journal of traditional and complementary medicine · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Synthesis ofFrontiers in chemistry · 2018
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. 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

12 authors at 3 institutions in 1 country.

L I NagyAVIDIN Ltd., Alsókikötő Sor 11, Szeged, Hungary.
L Z FehérAVIDIN Ltd., Alsókikötő Sor 11, Szeged, Hungary.
G J SzebeniAVIDIN Ltd., Alsókikötő Sor 11, Szeged, Hungary.
M GyurisAVIDIN Ltd., Alsókikötő Sor 11, Szeged, Hungary.
P SiposDepartment of Pharmaceutical Technology, University of Szeged, Eötvös u 6, Szeged 6720, Hungary.
R AlföldiAVIDIN Ltd., Alsókikötő Sor 11, Szeged, Hungary.
B ÓzsváriAVIDIN Ltd., Alsókikötő Sor 11, Szeged, Hungary.
L HacklerAVIDIN Ltd., Alsókikötő Sor 11, Szeged, Hungary.
A BalázsAVIDIN Ltd., Alsókikötő Sor 11, Szeged, Hungary.
P BatárDepartment of Hematology, Institute of Internal Medicine, University of Debrecen, Nagyerdei Körút 98, Debrecen 4032, Hungary.
I KanizsaiAVIDIN Ltd., Alsókikötő Sor 11, Szeged, Hungary.
L G PuskásAVIDIN Ltd., Alsókikötő Sor 11, Szeged, Hungary ; Institute of Genetics, Biological Research Center of the Hungarian Academy of Sciences, Temesvári Körút 62, Szeged 6726, Hungary.
Hungarian Academy of Sciences · HUUniversity of Debrecen · HUUniversity of Szeged · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Combination therapy of bortezomib with other chemotherapeutics is an emerging treatment strategy. Since both curcumin and bortezomib inhibit NF-κB, we tested the effects of their combination on leukemia cells. To improve potency, a novel Mannich-type curcumin derivative, C-150, was synthesized. Curcumin and its analogue showed potent antiproliferative and apoptotic effects on the human leukemia cell line, HL60, with different potency but similar additive properties with bortezomib. Additive antiproliferative effects were correlated well with LPS-induced NF-κB inhibition results. Gene expression data on cell cycle and apoptosis related genes, obtained by high-throughput QPCR, showed that curcumin and its analogue act through similar signaling pathways. In correlation with in vitro results similar additive effect could be obsereved in SCID mice inoculated systemically with HL60 cells. C-150 in a liposomal formulation given intravenously in combination with bortezomib was more efficient than either of the drugs alone. As our novel curcumin analogue exerted anticancer effects in leukemic cells at submicromolar concentration in vitro and at 3 mg/kg dose in vivo, which was potentiated by bortezomib, it holds a great promise as a future therapeutic agent in the treatment of leukemia alone or in combination.

Indexed as

AnimalsApoptosisBortezomibCurcuminHL-60 CellsHumansLeukemiaMiceMice, SCIDXenograft Model Antitumor AssaysBortezomibCurcumin

Identifiers

PMID26075279
PMCPMC4449904
OpenAlexW1483394052

What OpenQuestion holds

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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.