Evidence map›Paper›PMID 29679250›Full record

ArticleMarine biotechnology (New York, N.Y.)2018

The Marine Dinoflagellate Alexandrium andersoni Induces Cell Death in Lung and Colorectal Tumor Cell Lines.

Clementina Sansone, Genoveffa Nuzzo, Christian Galasso, Raffaella Casotti, Angelo Fontana, Giovanna Romano, Adrianna Ianora

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Marine biotechnology (New York, N.Y.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Marine drugs · 2023
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. An In Vitro Model to Investigate the Role ofInternational journal of molecular sciences · 2020
    Article
  9. Article
  10. Article
  11. Review
  12. The Marine DinoflagellateMarine drugs · 2018
    Article
  13. 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

7 authors at 1 institution in 1 country.

Clementina SansoneStazione Zoologica Anton Dohrn, Villa Comunale, 80121, Naples, Italy. clementina.sansone@szn.it.
Genoveffa NuzzoBio-Organic Chemistry Unit, Institute of Biomolecular Chemistry-CNR, Via Campi Flegrei 34, Pozzuoli, 80078, Naples, Italy.
Christian GalassoStazione Zoologica Anton Dohrn, Villa Comunale, 80121, Naples, Italy.
Raffaella CasottiStazione Zoologica Anton Dohrn, Villa Comunale, 80121, Naples, Italy.
Angelo FontanaBio-Organic Chemistry Unit, Institute of Biomolecular Chemistry-CNR, Via Campi Flegrei 34, Pozzuoli, 80078, Naples, Italy.
Giovanna RomanoStazione Zoologica Anton Dohrn, Villa Comunale, 80121, Naples, Italy.
Adrianna IanoraStazione Zoologica Anton Dohrn, Villa Comunale, 80121, Naples, Italy.
Stazione Zoologica Anton Dohrn · IT

Funding

European Marine Biological Research Infrastructure Cluster (EMBRIC) 654008Programma Operativo Nazionale 110_2093
6 · The paper itself

Abstract

Dinoflagellates are one of the most important components in marine phytoplankton, second only to diatoms as primary producers. Dinoflagellates have also been reported to produce bioactive secondary metabolites such as polyethers and macrolides with potential applications as pharmaceuticals. Here, we tested the effect of the organic extract and its related enriched extracts from solid-phase extraction (SPE) of a strain of the dinoflagellate Alexandrium andersoni. We found that the SPE extracts induced high cytotoxicity towards two cancer cell lines (A549 lung cancer and HT29 colorectal cancer) without affecting normal cell viability. The SPE extracts activated two different cell death pathways in the two tumor cell lines at the gene expression level, with the involvement of the major mediators of the tumor necrosis factor (TNF) cell signaling cascade. In HT29 cells, in addition to TNF activation, a death signaling pathway in response to DNA damage was also induced. This is an interesting finding since the HT29 cell line is highly aggressive since it is p53 gene-defect and this DNA instability renders this type of cancer very resistant towards all chemotherapeutic agents. Another significant result is that two distinct chemical fractions were selectively able to induce different and specific responses on the two different tumor cells treated.

Indexed as

A549 CellsAntineoplastic AgentsCell DeathCell Line, TumorCell SurvivalDinoflagellidaHT29 CellsHumansSignal TransductionSolid-Phase Synthesis TechniquesAntineoplastic AgentsA549Alexandrium andersoniHT29Marine bioactive dinoflagellateSPE fractionationTNF death signaling pathways

Identifiers

PMID29679250
OpenAlexW2801273964

What OpenQuestion holds

Textmetadata
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.