Evidence map›Paper›PMID 27825113›Full record

ArticleOncotarget2016

Marine guanidine alkaloids crambescidins inhibit tumor growth and activate intrinsic apoptotic signaling inducing tumor regression in a colorectal carcinoma zebrafish xenograft model.

María Roel, Juan A Rubiolo, Jorge Guerra-Varela, Siguara B L Silva, Olivier P Thomas, Pablo Cabezas-Sainz, Laura Sánchez, Rafael López, Luis M Botana

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

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  11. Structure-Activity Relationship of Cytotoxic Natural Products from Indonesian Marine Sponges.Revista brasileira de farmacognosia : orgao oficial da Sociedade Brasileira de Farmacognosia · 2022
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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

9 authors at 4 institutions in 3 countries.

María RoelDepartment of Pharmacology, Universidade de Santiago de Compostela, Campus Lugo, 27002 Lugo, Spain.
Juan A RubioloDepartment of Pharmacology, Universidade de Santiago de Compostela, Campus Lugo, 27002 Lugo, Spain.
Jorge Guerra-VarelaDepartment of Genetics, Universidade de Santiago de Compostela, Campus Lugo, 27002 Lugo, Spain.
Siguara B L SilvaGeoazur, UMR Université Nice Sophia Antipolis-CNRS-IRD-OCA, 06560 Valbonne, France.
Olivier P ThomasGeoazur, UMR Université Nice Sophia Antipolis-CNRS-IRD-OCA, 06560 Valbonne, France.
Pablo Cabezas-SainzDepartment of Genetics, Universidade de Santiago de Compostela, Campus Lugo, 27002 Lugo, Spain.
Laura SánchezDepartment of Genetics, Universidade de Santiago de Compostela, Campus Lugo, 27002 Lugo, Spain.
Rafael LópezTranslational Medical Oncology, Health Research Institute of Santiago (IDIS), Complexo Hospitalario Universitario de Santiago de Compostela (SERGAS), 15706 Santiago de Compostela, Spain.
Luis M BotanaDepartment of Pharmacology, Universidade de Santiago de Compostela, Campus Lugo, 27002 Lugo, Spain.
Universidade de Santiago de Compostela · ESCentre National de la Recherche Scientifique · FRComplexo Hospitalario Universitario A Coruña · ESUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The marine environment constitutes an extraordinary resource for the discovery of new therapeutic agents. In the present manuscript we studied the effect of 3 different sponge derived guanidine alkaloids, crambescidine-816, -830, and -800. We show that these compounds strongly inhibit tumor cell proliferation by down-regulating cyclin-dependent kinases 2/6 and cyclins D/A expression while up-regulating the cell cyclin-dependent kinase inhibitors -2A, -2D and -1A. We also show that these guanidine compounds disrupt tumor cell adhesion and cytoskeletal integrity promoting the activation of the intrinsic apoptotic signaling, resulting in loss of mitochondrial membrane potential and concomitant caspase-3 cleavage and activation. The crambescidin 816 anti-tumor effect was fnally assayed in a zebrafish xenotransplantation model confirming its potent antitumor activity against colorectal carcinoma in vivo.Considering these results crambescidins could represent promising natural anticancer agents and therapeutic tools.

Indexed as

AlkaloidsAnimalsAntineoplastic AgentsApoptosisCaspase 3Cell AdhesionCell Cycle ProteinsCell ProliferationCell SurvivalColorectal NeoplasmsCytoskeletonDose-Response Relationship, DrugG1 Phase Cell Cycle CheckpointsGuanidineHep G2 CellsHT29 CellsAlkaloidsAntineoplastic AgentsCASP3 protein, humanCaspase 3Cell Cycle Proteinscrambescidin 800crambescidin 816GuanidineSpiro Compoundsapoptosiscancer treatmentcell cycle inhibitioncrambescidinszebrafish xenograft model

Identifiers

PMID27825113
PMCPMC5347754
OpenAlexW2548493717

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.