Evidence map›Paper›PMID 29396431›Full record

ArticleCell death & disease2018

Game-changing restraint of Ros-damaged phenylalanine, upon tumor metastasis.

Geraldine Gueron, Nicolás Anselmino, Paula Chiarella, Emiliano G Ortiz, Sofia Lage Vickers, Alejandra V Paez, Jimena Giudice, Mario D Contin, Daiana Leonardi, Felipe Jaworski and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  8. Toxicity ofPlants (Basel, Switzerland) · 2021
    Review
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  12. Article
  13. Lessons from Hippocrates: Time to Change the Cancer Paradigm.International journal of chronic diseases · 2020
    Review
  14. Article
  15. 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

21 authors at 6 institutions in 2 countries.

Geraldine GueronDepartamento de Química Biológica, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Laboratorio de inflamación y Cáncer, Buenos Aires, Argentina. ggueron@gmail.com.ORCID 0000-0002-9283-7451
Nicolás AnselminoDepartamento de Química Biológica, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Laboratorio de inflamación y Cáncer, Buenos Aires, Argentina.
Paula ChiarellaLaboratory of Experimental Oncology, IMEX-CONICET (National Council of Scientific and Technical Research), National Academy of Medicine, Buenos Aires, Argentina.
Emiliano G OrtizDepartamento de Química Biológica, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Laboratorio de inflamación y Cáncer, Buenos Aires, Argentina.
Sofia Lage VickersDepartamento de Química Biológica, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Laboratorio de inflamación y Cáncer, Buenos Aires, Argentina.
Alejandra V PaezDepartamento de Química Biológica, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Laboratorio de inflamación y Cáncer, Buenos Aires, Argentina.
Jimena GiudiceDepartment of Cell Biology and Physiology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Mario D ContinDepartment of Organic Chemistry, CIHIDECAR-CONICET, FCEN, University of Buenos Aires, Buenos Aires, Argentina.
Daiana LeonardiDepartamento de Química Biológica, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Laboratorio de inflamación y Cáncer, Buenos Aires, Argentina.
Felipe JaworskiDepartamento de Química Biológica, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Laboratorio de inflamación y Cáncer, Buenos Aires, Argentina.
Verónica ManzanoDepartment of Cell Biology and Physiology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Ariel StrazzaLaboratory of Experimental Oncology, IMEX-CONICET (National Council of Scientific and Technical Research), National Academy of Medicine, Buenos Aires, Argentina.
Daniela R MontagnaLaboratory of Experimental Oncology, IMEX-CONICET (National Council of Scientific and Technical Research), National Academy of Medicine, Buenos Aires, Argentina.
Estefania LabancaDepartment of Pharmacology and Therapeutics, Roswell Park Cancer Institute, Buffalo, NY, USA.
Javier CotignolaDepartamento de Química Biológica, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Laboratorio de inflamación y Cáncer, Buenos Aires, Argentina.ORCID 0000-0003-4473-9854
Norma D AccorsoDepartment of Organic Chemistry, CIHIDECAR-CONICET, FCEN, University of Buenos Aires, Buenos Aires, Argentina.
Anna Woloszynska-ReadDepartment of Genitourinary Medical Oncology, The University of Texas, M.D. Anderson Cancer Center, Houston, TX, USA.
Nora NavoneDepartment of Pharmacology and Therapeutics, Roswell Park Cancer Institute, Buffalo, NY, USA.
Roberto P MeissLaboratory of Pathology, Institute of Oncological studies (IEO) National Academy of Medicine, Buenos Aires, Argentina.
Raúl RuggieroLaboratory of Experimental Oncology, IMEX-CONICET (National Council of Scientific and Technical Research), National Academy of Medicine, Buenos Aires, Argentina. ruloruggiero@yahoo.com.ar.
Elba VazquezDepartamento de Química Biológica, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Laboratorio de inflamación y Cáncer, Buenos Aires, Argentina. elba@qb.fcen.uba.ar.
Consejo Nacional de Investigaciones Científicas y Técnicas · ARAcademia Nacional de Medicina · ARRoswell Park Comprehensive Cancer Center · USUniversity of North Carolina at Chapel Hill · USThe University of Texas MD Anderson Cancer Center · USUniversidad de Buenos Aires · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An abrupt increase in metastatic growth as a consequence of the removal of primary tumors suggests that the concomitant resistance (CR) phenomenon might occur in human cancer. CR occurs in murine tumors and ROS-damaged phenylalanine, meta-tyrosine (m-Tyr), was proposed as the serum anti-tumor factor primarily responsible for CR. Herein, we demonstrate for the first time that CR happens in different experimental human solid tumors (prostate, lung anaplastic, and nasopharyngeal carcinoma). Moreover, m-Tyr was detected in the serum of mice bearing prostate cancer (PCa) xenografts. Primary tumor growth was inhibited in animals injected with m-Tyr. Further, the CR phenomenon was reversed when secondary implants were injected into mice with phenylalanine (Phe), a protective amino acid highly present in primary tumors. PCa cells exposed to m-Tyr in vitro showed reduced cell viability, downregulated NFκB/STAT3/Notch axis, and induced autophagy; effects reversed by Phe. Strikingly, m-Tyr administration also impaired both, spontaneous metastasis derived from murine mammary carcinomas (4T1, C7HI, and LMM3) and PCa experimental metastases. Altogether, our findings propose m-Tyr delivery as a novel approach to boost the therapeutic efficacy of the current treatment for metastasis preventing the escape from tumor dormancy.

Indexed as

AnimalsCell Line, TumorCell ProliferationDown-RegulationDrug Resistance, NeoplasmHumansMaleMice, NudeNeoplasm MetastasisPhenylalanineProstatic NeoplasmsReactive Oxygen SpeciesSerumSignal TransductionSubcutaneous TissueTyrosine3-tyrosinePhenylalanineReactive Oxygen SpeciesTyrosine

Identifiers

PMID29396431
PMCPMC5833805
OpenAlexW2791496571

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.