Evidence map›Paper›PMID 31200739›Full record

ReviewJournal of experimental & clinical cancer research : CR2019

Autophagy manipulation as a strategy for efficient anticancer therapies: possible consequences.

Mara Cirone, Maria Saveria Gilardini Montani, Marisa Granato, Alessia Garufi, Alberto Faggioni, Gabriella D'Orazi

Open access · goldAbstract readReview
In one paragraph

Review in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
7.7field-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

40 citing papers in PubMed, 63 citations in OpenAlex.

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  14. Dichotomous role of autophagy in cancer.Asian biomedicine : research, reviews and news · 2022
    Review
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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

6 authors at 2 institutions in 2 countries.

Mara CironeDepartment of Experimental Medicine, "Sapienza" University of Rome, Rome, Italy. mara.cirone@uniroma1.it.
Maria Saveria Gilardini MontaniDepartment of Experimental Medicine, "Sapienza" University of Rome, Rome, Italy.
Marisa GranatoDepartment of Experimental Medicine, "Sapienza" University of Rome, Rome, Italy.
Alessia GarufiDepartment of Medical Science, University 'G. D'Annunzio', 66013, Chieti, Italy.
Alberto FaggioniDepartment of Experimental Medicine, "Sapienza" University of Rome, Rome, Italy.
Gabriella D'OraziDepartment of Medical Science, University 'G. D'Annunzio', 66013, Chieti, Italy. gdorazi@unich.it.ORCID http://orcid.org/0000-0001-6876-9105
Istituto Pasteur · ITUniversity of Chieti-Pescara · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG2015, 16742Istituto Pasteur-Fondazione Cenci Bolognetti n. C26A
6 · The paper itself

Abstract

Autophagy is a catabolic process whose activation may help cancer cells to adapt to cellular stress although, in some instances, it can induce cell death. Autophagy stimulation or inhibition has been considered an opportunity to treat cancer, especially in combination with anticancer therapies, although autophagy manipulation may be viewed as controversial. Thus, whether to induce or to inhibit autophagy may be the best option in the different cancer patients is still matter of debate. Her we will recapitulate the possible advantages or disadvantages of manipulating autophagy in cancer, not only with the aim to obtain cancer cell death and disable oncogenes, but also to evaluate its interplay with the immune response which is fundamental for the success of anticancer therapies.

Indexed as

AnimalsAntineoplastic AgentsApoptosisAutophagyEndoplasmic Reticulum StressGene Expression Regulation, NeoplasticHumansMolecular Targeted TherapyNeoplasmsOncogenesSignal TransductionUnfolded Protein ResponseAntineoplastic AgentsAutophagyCancerChloroquine (CQ)Endoplasmic reticulum (ER stress)HSF1Hydroxichloroquine (HCQ)Immunogenic cell death (ICD)NRF2p53Unfolded protein response (UPR)

Identifiers

PMID31200739
PMCPMC6570888
OpenAlexW2952026773

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.