Evidence map›Paper›PMID 38396682›Full record

ArticleInternational journal of molecular sciences2024

Persistence of Chronic Lymphocytic Leukemia Stem-like Populations under Simultaneous In Vitro Treatment with Curcumin, Fludarabine, and Ibrutinib: Implications for Therapy Resistance.

Àngel Bistué-Rovira, Laura G Rico, Jorge Bardina, Jordi Juncà, Isabel Granada, Jolene A Bradford, Michael D Ward, Roser Salvia, Francesc Solé, Jordi Petriz

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

10 authors at 4 institutions in 2 countries.

Àngel Bistué-RoviraDepartament de Farmacologia, Terapèutica i Toxicologia, Universitat Autònoma de Barcelona (UAB), 08193 Cerdanyola del Vallès, Spain.
Laura G RicoGermans Trias i Pujol Research Institute (IGTP), Universitat Autònoma de Barcelona (UAB), 08916 Badalona, Spain.ORCID 0000-0001-9867-4393
Jorge BardinaVall d'Hebron Institute of Oncology (VHIO), 08035 Barcelona, Spain.
Jordi JuncàMDS Group, Institut de Recerca Contra la Leucèmia Josep Carreras, 08916 Badalona, Spain.
Isabel GranadaMDS Group, Institut de Recerca Contra la Leucèmia Josep Carreras, 08916 Badalona, Spain.
Jolene A BradfordThermo Fisher Scientific, Fort Collins, CO 80524, USA.
Michael D WardThermo Fisher Scientific, Fort Collins, CO 80524, USA.
Roser SalviaGermans Trias i Pujol Research Institute (IGTP), Universitat Autònoma de Barcelona (UAB), 08916 Badalona, Spain.ORCID 0000-0002-2118-9231
Francesc SoléMDS Group, Institut de Recerca Contra la Leucèmia Josep Carreras, 08916 Badalona, Spain.ORCID 0000-0002-3251-2161
Jordi PetrizGermans Trias i Pujol Research Institute (IGTP), Universitat Autònoma de Barcelona (UAB), 08916 Badalona, Spain.
Universitat Autònoma de Barcelona · ESFundación Josep Carreras Contra la Leucemia · ESThermo Fisher Scientific (United States) · USVall d'Hebron Institute of Oncology · ES

Funding

CERCA Institution NAThermo Fisher Scientific (Norway) NA
6 · The paper itself

Abstract

Leukemic stem cells (LSCs) possess similar characteristics to normal hematopoietic stem cells, including self-renewal capacity, quiescence, ability to initiate leukemia, and drug resistance. These cells play a significant role in leukemia relapse, persisting even after apparent remission. LSCs were first described in 1994 by Lapidot et al. Although they have been extensively studied in acute leukemia, more LSC research is still needed in chronic lymphocytic leukemia (CLL) to understand if reduced apoptosis in mature cells should still be considered as the major cause of this disease. Here, we provide new evidence suggesting the existence of stem-like cell populations in CLL, which may help to understand the disease as well as to develop effective treatments. In this study, we identified a potential leukemic stem cell subpopulation using the tetraploid CLL cell line I83. This subpopulation is characterized by diploid cells that were capable of generating the I83 tetraploid population. Furthermore, we adapted a novel flow cytometry analysis protocol to detect CLL subpopulations with stem cell properties in peripheral blood samples and primary cultures from CLL patients. These cells were identified by their co-expression of CD19 and CD5, characteristic markers of CLL cells. As previously described, increased alkaline phosphatase (ALP) activity is indicative of stemness and pluripotency. Moreover, we used this method to investigate the potential synergistic effect of curcumin in combination with fludarabine and ibrutinib to deplete this subpopulation. Our results confirmed the effectiveness of this ALP-based analysis protocol in detecting and monitoring leukemic stem-like cells in CLL. This analysis also identified limitations in eradicating these populations using in vitro testing. Furthermore, our findings demonstrated that curcumin significantly enhanced the effects of fludarabine and ibrutinib on the leukemic fraction, exhibiting synergistic effects (combination drug index, CDI 0.97 and 0.37, respectively). Our results lend support to the existence of potential stem-like populations in CLL cell lines, and to the idea that curcumin could serve as an effective adjuvant in therapies aimed at eliminating these populations and improving treatment efficacy.

Indexed as

CurcuminLeukemia, Lymphocytic, Chronic, B-CellPiperidinesAdenineHumansTetraploidyVidarabineAdenineCurcuminfludarabineibrutinibPiperidinesVidarabinealkaline phosphataseCLLcurcuminflow cytometryLSCsstem-like

Identifiers

PMID38396682
PMCPMC10888954
OpenAlexW4391605980

What OpenQuestion holds

Textmetadata
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.