Evidence map›Paper›PMID 29587347›Full record

ReviewInternational journal of molecular sciences2018

Survivin-Based Treatment Strategies for Squamous Cell Carcinoma.

Andrea Santarelli, Marco Mascitti, Lucio Lo Russo, Davide Sartini, Giuseppe Troiano, Monica Emanuelli, Lorenzo Lo Muzio

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

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

  1. Pooled it
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  11. Dual role of deubiquitinating enzyme USP19 regulates mitotic progression and tumorigenesis by stabilizing survivin.Molecular therapy : the journal of the American Society of Gene Therapy · 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

7 authors at 2 institutions in 1 country.

Andrea SantarelliDepartment of Clinical Specialistic and Dental Sciences, Marche Polytechnic University, Via Tronto 10, 60126 Ancona, Italy. andrea.santarelli@staff.univpm.it.
Marco MascittiDepartment of Clinical Specialistic and Dental Sciences, Marche Polytechnic University, Via Tronto 10, 60126 Ancona, Italy. marcomascitti86@hotmail.it.ORCID 0000-0002-7304-3752
Lucio Lo RussoDepartment of Clinical and Experimental Medicine, Foggia University, Via Rovelli 50, 71122 Foggia, Italy. lucio.lorusso@unifg.it.ORCID 0000-0001-6127-6105
Davide SartiniDepartment of Clinical Specialistic and Dental Sciences, Marche Polytechnic University, Via Tronto 10, 60126 Ancona, Italy. davide_sartini@libero.it.
Giuseppe TroianoDepartment of Clinical and Experimental Medicine, Foggia University, Via Rovelli 50, 71122 Foggia, Italy. giuseppe.troiano@unifg.it.
Monica EmanuelliDepartment of Clinical Specialistic and Dental Sciences, Marche Polytechnic University, Via Tronto 10, 60126 Ancona, Italy. m.emanuelli@univpm.it.
Lorenzo Lo MuzioDepartment of Clinical and Experimental Medicine, Foggia University, Via Rovelli 50, 71122 Foggia, Italy. lorenzo.lomuzio@unifg.it.ORCID 0000-0003-4633-4893
Marche Polytechnic University · ITUniversity of Foggia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Survivin, an anti-apoptotic molecule abundantly expressed in most human neoplasms, has been reported to contribute to cancer initiation and drug resistance in a wide variety of human tumors. Efficient downregulation of survivin can sensitize tumor cells to various therapeutic interventions, generating considerable efforts in its validation as a new target in cancer therapy. This review thoroughly analyzes up-to-date information on the potential of survivin as a therapeutic target for new anticancer treatments. The literature dealing with the therapeutic targeting of survivin will be reviewed, discussing specifically squamous cell carcinomas (SCCs), and with emphasis on the last clinical trials. This review gives insight into the recent developments undertaken in validating various treatment strategies that target survivin in SCCs and analyze the translational possibility, identifying those strategies that seem to be the closest to being incorporated into clinical practice. The most recent developments, such as dominant-negative survivin mutants, RNA interference, anti-sense oligonucleotides, small-molecule inhibitors, and peptide-based immunotherapy, seem to be helpful for effectively downregulating survivin expression and reducing tumor growth potential, increasing the apoptotic rate, and sensitizing tumor cells to chemo- and radiotherapy. However, selective and efficient targeting of survivin in clinical trials still poses a major challenge.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCarcinoma, Squamous CellCell ProliferationClinical Trials as TopicGenetic TherapyHumansImmunotherapyInhibitor of Apoptosis ProteinsMiceMolecular Targeted TherapyMouth NeoplasmsOligonucleotides, AntisenseRNA InterferenceSurvivinAntineoplastic AgentsBIRC5 protein, humanInhibitor of Apoptosis ProteinsOligonucleotides, AntisenseSurvivininhibitor of apoptosisoral squamous cell carcinomasquamous cell carcinomasurvivin

Identifiers

PMID29587347
PMCPMC5979467
OpenAlexW2790347368

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.