Evidence map›Paper›PMID 31371410›Full record

ArticleHaematologica2020

Leprosy drug clofazimine activates peroxisome proliferator-activated receptor-γ and synergizes with imatinib to inhibit chronic myeloid leukemia cells.

Harish Kumar, Sourav Chattopadhyay, Nabanita Das, Sonal Shree, Dinesh Patel, Jogeswar Mohapatra, Anagha Gurjar, Sapana Kushwaha, Abhishek Kumar Singh, Shikha Dubey and 15 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Proteomic analysis and identification reveal the anti-inflammatory mechanism of clofazimine on lipopolysaccharide-induced acute lung injury in mice.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Article
  6. Molecular design of a pathogen activated, self-assembling mechanopharmaceutical device.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Review
  7. Article
  8. Article
  9. International journal of biological sciences · 2022
    Article
  10. Review
  11. Article
  12. Wnt Signaling in Leukemia and Its Bone Marrow Microenvironment.International journal of molecular sciences · 2020
    Review
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

25 authors at 5 institutions in 1 country.

Harish KumarDivision of Biochemistry, CSIR-Central Drug Research Institute, Lucknow.
Sourav ChattopadhyayDivision of Biochemistry, CSIR-Central Drug Research Institute, Lucknow.
Nabanita DasDivision of Biochemistry, CSIR-Central Drug Research Institute, Lucknow.
Sonal ShreeDivision of Molecular and Structural Biology, CSIR-Central Drug Research Institute, Lucknow.
Dinesh PatelZydus Research Center, Moraiya, Ahmedabad, Gujarat.
Jogeswar MohapatraZydus Research Center, Moraiya, Ahmedabad, Gujarat.
Anagha GurjarDivision of Biochemistry, CSIR-Central Drug Research Institute, Lucknow.
Sapana KushwahaDivision of Biochemistry, CSIR-Central Drug Research Institute, Lucknow.
Abhishek Kumar SinghDivision of Biochemistry, CSIR-Central Drug Research Institute, Lucknow.
Shikha DubeyDivision of Molecular and Structural Biology, CSIR-Central Drug Research Institute, Lucknow.
Kiran LataDivision of Molecular and Structural Biology, CSIR-Central Drug Research Institute, Lucknow.
Rajesh KushwahaDevelopmental Toxicology Laboratory, Systems Toxicology and Health Risk Assessment Group, CSIR-Indian Institute of Toxicology Research, Lucknow.
Riyazuddin MohammedPharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Lucknow.
Krishnarup Ghosh DastidarZydus Research Center, Moraiya, Ahmedabad, Gujarat.
Namrata YadavZydus Research Center, Moraiya, Ahmedabad, Gujarat.
Achchhe Lal VishwakarmaSophisticated Analytical Instrument Facility, CSIR-Central Drug Research Institute, Lucknow.
Jiaur Rahaman GayenPharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Lucknow.
Sanghamitra BandyopadhyayDevelopmental Toxicology Laboratory, Systems Toxicology and Health Risk Assessment Group, CSIR-Indian Institute of Toxicology Research, Lucknow.
Abhijit ChatterjeeZydus Research Center, Moraiya, Ahmedabad, Gujarat.
Mukul Rameshchandra JainZydus Research Center, Moraiya, Ahmedabad, Gujarat.
Anil Kumar TripathiDepartment of Clinical Hematology and Medical Oncology, King George's Medical University, Lucknow, Uttar Pradesh.
Arun Kumar TrivediDivision of Biochemistry, CSIR-Central Drug Research Institute, Lucknow.
Naibedya ChattopadhyayDivision of Endocrinology, CSIR-Central Drug Research Institute, Lucknow, India.
Ravishankar RamachandranAcSIR, CSIR-Central Drug Research Institute Campus, Lucknow.
Sabyasachi SanyalDivision of Biochemistry, CSIR-Central Drug Research Institute, Lucknow sanyal@cdri.res.in.
Central Drug Research Institute · INCadila Healthcare (India) · INAcademy of Scientific and Innovative Research · INIndian Institute of Toxicology Research · INKing George's Medical University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leukemia stem cells contribute to drug-resistance and relapse in chronic myeloid leukemia (CML) and BCR-ABL1 inhibitor monotherapy fails to eliminate these cells, thereby necessitating alternate therapeutic strategies for patients CML. The peroxisome proliferator-activated receptor-γ (PPARγ) agonist pioglitazone downregulates signal transducer and activator of transcription 5 (STAT5) and in combination with imatinib induces complete molecular response in imatinib-refractory patients by eroding leukemia stem cells. Thiazolidinediones such as pioglitazone are, however, associated with severe side effects. To identify alternate therapeutic strategies for CML we screened Food and Drug Administration-approved drugs in K562 cells and identified the leprosy drug clofazimine as an inhibitor of viability of these cells. Here we show that clofazimine induced apoptosis of blood mononuclear cells derived from patients with CML, with a particularly robust effect in imatinib-resistant cells. Clofazimine also induced apoptosis of CD34

Indexed as

LeprosyLeukemia, Myelogenous, Chronic, BCR-ABL PositivePharmaceutical PreparationsApoptosisClofazimineDrug Resistance, NeoplasmFusion Proteins, bcr-ablHumansImatinib MesylateK562 CellsPPAR gammaClofazimineFusion Proteins, bcr-ablImatinib MesylatePharmaceutical PreparationsPPAR gamma

Identifiers

PMID31371410
PMCPMC7109729
OpenAlexW2964643846

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.