Evidence map›Paper›PMID 32152409›Full record

ArticleScientific reports2020

Mitochondria as target to inhibit proliferation and induce apoptosis of cancer cells: the effects of doxycycline and gemcitabine.

Sas N Dijk, Margherita Protasoni, Marilena Elpidorou, Albert M Kroon, Jan-Willem Taanman

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

64 citing papers in PubMed, 96 citations in OpenAlex.

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  13. Mitochondrial Ribosomal Proteins and Cancer.Medicina (Kaunas, Lithuania) · 2025
    Review
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  15. Article
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4 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Sas N DijkResearch Department of Surgical Biotechnology, Division of Surgery and Interventional Science, University College London, London, NW3 2PF, UK.
Margherita ProtasoniDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, NW3 2PF, UK.
Marilena ElpidorouDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, NW3 2PF, UK.
Albert M KroonDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, NW3 2PF, UK.
Jan-Willem TaanmanDepartment of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, NW3 2PF, UK. j.taanman@ucl.ac.uk.
King's College London · GBUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Doxycycline has anti-tumour effects in a range of tumour systems. The aims of this study were to define the role mitochondria play in this process and examine the potential of doxycycline in combination with gemcitabine. We studied the adenocarcinoma cell line A549, its mitochondrial DNA-less derivative A549 ρ° and cultured fibroblasts. Treatment with doxycycline for 5 days resulted in a decrease of mitochondrial-encoded proteins, respiration and membrane potential, and an increase of reactive oxygen species in A549 cells and fibroblasts, but fibroblasts were less affected. Doxycycline slowed proliferation of A549 cells by 35%. Cellular ATP levels did not change. Doxycycline alone had no effect on apoptosis; however, in combination with gemcitabine given during the last 2 days of treatment, doxycycline increased caspase 9 and 3/7 activities, resulting in a further decrease of surviving A549 cells by 59% and of fibroblasts by 24% compared to gemcitabine treatment alone. A549 ρ° cells were not affected by doxycycline. Key effects of doxycycline observed in A549 cells, such as the decrease of mitochondrial-encoded proteins and surviving cells were also seen in the cancer cell lines COLO357 and HT29. Our results suggest that doxycycline suppresses cancer cell proliferation and primes cells for apoptosis by gemcitabine.

Indexed as

Adenosine TriphosphateAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationCell RespirationCell SurvivalDeoxycytidineDNA Copy Number VariationsDNA, MitochondrialDoxycyclineGemcitabineGene Expression Regulation, EnzymologicGlycolysisHumansMembrane Potential, MitochondrialAdenosine TriphosphateAntineoplastic AgentsDeoxycytidineDNA, MitochondrialDoxycyclineGemcitabineReactive Oxygen Species

Identifiers

PMID32152409
PMCPMC7063048
OpenAlexW3010591636

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.