Evidence map›Paper›PMID 34055641›Full record

ArticleFrontiers in oncology2021

Clinical Relevance of ABCB1, ABCG2, and ABCC2 Gene Polymorphisms in Chronic Myeloid Leukemia Patients Treated With Nilotinib.

Federica Loscocco, Giuseppe Visani, Annamaria Ruzzo, Irene Bagaloni, Fabio Fuligni, Sara Galimberti, Antonello Di Paolo, Fabio Stagno, Patrizia Pregno, Mario Annunziata and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Genomics in Health and Biomedicine.Advances in experimental medicine and biology · 2026
    Review
  2. Review
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  5. Article
  6. Review
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  8. Article
  9. Two Important Anticancer Mechanisms of Natural and Synthetic Chalcones.International journal of molecular sciences · 2022
    Review
  10. Review
  11. Article
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  13. Pharmacogenomics in Targeted Therapy and Supportive Care Therapies for Cancer.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  14. 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

15 authors at 5 institutions in 2 countries.

Federica LoscoccoHematology and Hematopoietic Stem Cell Transplant Center, AORMN, Pesaro, Italy.
Giuseppe VisaniHematology and Hematopoietic Stem Cell Transplant Center, AORMN, Pesaro, Italy.
Annamaria RuzzoDepartment of Biomolecular Sciences, University of Urbino "Carlo Bo", Fano, Italy.
Irene BagaloniDepartment of Biomolecular Sciences, University of Urbino "Carlo Bo", Fano, Italy.
Fabio FuligniGenetics and Genome Biology, Paediatric Laboratory Medicine (PLM), The Hospital for Sick Children, Toronto, ON, Canada.
Sara GalimbertiDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Antonello Di PaoloDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Fabio StagnoAOU Policlinico Vittorio Emanuele, Divisioni Clinicizzata di Ematologia con Trapianto di Midollo Osseo, Catania, Italy.
Patrizia PregnoAOU Città Della Scienza e Della Salute di Torino, Hematology, Torino, Italy.
Mario AnnunziataHematology, Cardarelli Hospital, Napoli, Italy.
Antonella GozziniAOU Careggi, Unità funzionale di Ematologia, Firenze, Italy.
Sara BarulliHematology and Hematopoietic Stem Cell Transplant Center, AORMN, Pesaro, Italy.
Elisa GabucciHematology and Hematopoietic Stem Cell Transplant Center, AORMN, Pesaro, Italy.
Mauro MagnaniDepartment of Biomolecular Sciences, University of Urbino "Carlo Bo", Fano, Italy.
Alessandro IsidoriHematology and Hematopoietic Stem Cell Transplant Center, AORMN, Pesaro, Italy.
University of Urbino · ITUniversity of Pisa · ITAzienda Ospedaliera Citta' della Salute e della Scienza di Torino · ITAzienda Ospedaliero-Universitaria Careggi · ITHospital for Sick Children · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tyrosine kinase inhibitors (TKIs) have radically changed the outcome of chronic myeloid leukemia (CML) patients in the last 20 years. Moreover, the advent of second generation TKIs, namely nilotinib and dasatinib, have largely increased the number of CML patients achieving deep and sustained molecular responses. However, the possible mechanisms capable of influencing the maintenance of the long-term molecular response are not yet fully known and understood. In this light, polymorphisms in MDR-ABC transporters may influence the efficacy and safety of TKIs. In this study, we examined seven single nucleotide polymorphisms (SNPs) in four ABC transporter genes: ABCC1 rs212090 (5463T>A), ABCC2 rs3740066 (3972C>T), ABCC2 rs4148386 G>A, ABCC2 rs1885301 (1549G>A), ABCG2 rs2231137 (34G>A), ABCG2 rs2231142 G>C, ABCB1 rs1045642 (3435C>T), to determine their effect on the achievement and/or loss of molecular response in 90 CML patients treated with nilotinib. We found that

Indexed as

chronic myeloid leukemiadrug resistanceMDR-ABC transportersmolecular responsenilotinibpolymorphisms

Identifiers

PMID34055641
PMCPMC8155509
OpenAlexW3161448988

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.