Evidence map›Paper›PMID 35563141›Full record

ArticleInternational journal of molecular sciences2022

The Cooperative Anti-Neoplastic Activity of Polyphenolic Phytochemicals on Human T-Cell Acute Lymphoblastic Leukemia Cell Line MOLT-4 In Vitro.

Patrycja Koszałka, Grzegorz Stasiłojć, Natalia Miękus-Purwin, Maciej Niedźwiecki, Maciej Purwin, Szymon Grabowski, Tomasz Bączek

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 43% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. 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

7 authors at 1 institution in 1 country.

Patrycja KoszałkaInstitute of Medical Biotechnology and Experimental Oncology, Intercollegiate Faculty of Biotechnology, University of Gdańsk and Medical University of Gdańsk, Dębinki Street 1, 80-211 Gdańsk, Poland.ORCID 0000-0002-1224-5860
Grzegorz StasiłojćInstitute of Medical Biotechnology and Experimental Oncology, Intercollegiate Faculty of Biotechnology, University of Gdańsk and Medical University of Gdańsk, Dębinki Street 1, 80-211 Gdańsk, Poland.ORCID 0000-0002-4158-1935
Natalia Miękus-PurwinDepartment of Pharmaceutical Chemistry, Medical University of Gdańsk, Hallera Street 107, 80-416 Gdańsk, Poland.ORCID 0000-0002-9605-3259
Maciej NiedźwieckiDepartment of Pediatrics, Hematology and Oncology, Medical University of Gdansk, Debinki Street 7, 80-211 Gdańsk, Poland.
Maciej PurwinDepartment of Pharmaceutical Chemistry, Medical University of Gdańsk, Hallera Street 107, 80-416 Gdańsk, Poland.
Szymon GrabowskiGetResponse Cares Foundation, Arkońska Street 6/A3, 80-387 Gdańsk, Poland.
Tomasz BączekDepartment of Pharmaceutical Chemistry, Medical University of Gdańsk, Hallera Street 107, 80-416 Gdańsk, Poland.ORCID 0000-0001-6468-1974
Gdańsk Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lymphoblastic leukemia (ALL) is the most common hematological malignancy affecting pediatric patients. ALL treatment regimens with cytostatics manifest substantial toxicity and have reached the maximum of well-tolerated doses. One potential approach for improving treatment efficiency could be supplementation of the current regimen with naturally occurring phytochemicals with anti-cancer properties. Nutraceuticals such as quercetin, curcumin, resveratrol, and genistein have been studied in anti-cancer therapy, but their application is limited by their low bioavailability. However, their cooperative activity could potentially increase their efficiency at low, bioavailable doses. We studied their cooperative effect on the viability of a human ALL MOLT-4 cell line in vitro at the concentration considered to be in the bioavailable range in vivo. To analyze their potential side effect on the viability of non-tumor cells, we evaluated their toxicity on a normal human foreskin fibroblast cell line (BJ). In both cell lines, we also measured specific indicators of cell death, changes in cell membrane permeability (CMP), and mitochondrial membrane potential (MMP). Even at a low bioavailable concentration, genistein and curcumin decreased MOLT-4 viability, and their combination had a significant interactive effect. While resveratrol and quercetin did not affect MOLT-4 viability, together they enhanced the effect of the genistein/curcumin mix, significantly inhibiting MOLT-4 population growth in vitro. Moreover, the analyzed phytochemicals and their combinations did not affect the BJ cell line. In both cell lines, they induced a decrease in MMP and correlating CMP changes, but in non-tumor cells, both metabolic activity and cell membrane continuity were restored in time. (4) Conclusions: The results indicate that the interactive activity of analyzed phytochemicals can induce an anti-cancer effect on ALL cells without a significant effect on non-tumor cells. It implies that the application of the combinations of phytochemicals an anti-cancer treatment supplement could be worth further investigation regardless of their low bioavailability.

Indexed as

CurcuminPrecursor Cell Lymphoblastic Leukemia-LymphomaPrecursor T-Cell Lymphoblastic Leukemia-LymphomaApoptosisCell LineCell Line, TumorGenisteinHumansPhytochemicalsQuercetinResveratrolCurcuminGenisteinPhytochemicalsQuercetinResveratrolacute lymphoblastic leukemiaBJcell membrane permeabilitycurcumingenisteinmitochondrial membrane potentialMOLT-4quercetinresveratrol

Identifiers

PMID35563141
PMCPMC9099961
OpenAlexW4224984862

What OpenQuestion holds

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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.