Evidence map›Paper›PMID 28218707›Full record

ArticleInternational journal of molecular sciences2017

FKBP51 Immunohistochemical Expression: A New Prognostic Biomarker for OSCC?

Daniela Russo, Francesco Merolla, Massimo Mascolo, Gennaro Ilardi, Simona Romano, Silvia Varricchio, Virginia Napolitano, Angela Celetti, Loredana Postiglione, Pier Paolo Di Lorenzo and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.7field-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

21 citing papers in PubMed, 39 citations in OpenAlex.

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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

15 authors at 3 institutions in 1 country.

Daniela RussoDepartment of Advanced Biomedical Sciences, University "Federico II", 80131 Naples, Italy. danielarusso83@yahoo.it.
Francesco MerollaDepartment of Medicine and Health Sciences "V. Tiberio", University of Molise, 86100 Campobasso, Italy. francesco.merolla@unimol.it.
Massimo MascoloDepartment of Advanced Biomedical Sciences, University "Federico II", 80131 Naples, Italy. mmascol@gmail.com.
Gennaro IlardiDepartment of Advanced Biomedical Sciences, University "Federico II", 80131 Naples, Italy. gennaro.ilardi@gmail.com.
Simona RomanoDepartment of Molecular Medicine and Medical Biotechnology, University "Federico II", 80131 Naples, Italy. romanos@dbbm.unina.it.
Silvia VarricchioDepartment of Advanced Biomedical Sciences, University "Federico II", 80131 Naples, Italy. silvia.varricchio@gmail.com.
Virginia NapolitanoDepartment of Advanced Biomedical Sciences, University "Federico II", 80131 Naples, Italy. virnap87@hotmail.it.
Angela CelettiInstitute for the Experimental Endocrinology and Oncology, Research National Council, 80131 Naples, Italy. celetti@unina.it.
Loredana PostiglioneDepartment of Translational Medical Sciences and Center for Basic and Clinical Immunology Research, University "Federico II", 80131 Naples, Italy. loredana.postiglione@unina.it.
Pier Paolo Di LorenzoDepartment of Advanced Biomedical Sciences, University "Federico II", 80131 Naples, Italy. pierpaolo.dilorenzo@unina.it.
Luigi CalifanoDepartment of Maxillofacial Surgery, University "Federico II", 80131 Naples, Italy. califano@unina.it.
Giovanni Orabona Dell'AversanaDepartment of Maxillofacial Surgery, University "Federico II", 80131 Naples, Italy. giovanni.dellaversanaorabona@unina.it.
Fabio AstaritaDepartment of Maxillofacial Surgery, University "Federico II", 80131 Naples, Italy. dottastarita@gmail.com.
Maria Fiammetta RomanoDepartment of Molecular Medicine and Medical Biotechnology, University "Federico II", 80131 Naples, Italy. mariafiammetta.romano@unina.it.
Stefania StaibanoDepartment of Advanced Biomedical Sciences, University "Federico II", 80131 Naples, Italy. staibano@unina.it.
Federico II University Hospital · ITInstitute for Experimental Endocrinology and Oncology · ITUniversity of Molise · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Up-to-date, several molecular markers of prognosis have been studied in Oral Squamous Cell Carcinoma (OSCC), but none entered in the clinical setting. Therapy of OSCC tumors mainly relies on surgery, radiotherapy and partially on chemotherapy; there is an urgent need for biomarkers able to better stratify OSCC patients' risk to address targeted therapeutic strategies. The role of immune response in the pathogenesis and biological behavior of OSCC has been investigated by several authors, and promising results have been obtained with immune checkpoint inhibitors. We already investigated the role of the immune modulator FK506-binding protein 51 (FKBP51), a FK506-binding immunophilin, in cutaneous melanoma biology, and its expression in several human solid tumors. In the present study, we aimed to assess the value of FKBP51 expression in OSCC tumor cells as a marker of outcome. We collected clinical data from 72 patients who underwent surgery for Squamous Cell Carcinoma (SCC) of the tongue, floor, lips and palate. FKBP51 expression was assessed by immunohistochemistry on paraffin-embedded tumor tissues. In addition, we evaluated the human papillomavirus (HPV) status of primary tumors by immunohistochemistry, viral subtyping and In Situ Hybridization (ISH) assay. We found that high FKBP51-expressing tumors characterized the OSCCs with the worst prognosis: the high immunohistochemical expression of FKBP51 associated with death occurring within five years from the diagnosis with a sensitivity of 88.46% and a specificity of 91.67%. The estimated positive predictive value of the test was 88.45% and negative predictive value 91.67%. We tested FKBP51 mRNA presence, by RT-PCR assay, in a selected series of OSCC tumors, and we found that mRNA correlated well to the protein expression and to the clinical outcome. Applying the Bayes formula, we estimated an 88% probability of dying within five years from the diagnosis of OSCC patients with a high FKBP51 immunohistochemical (IHC) test result (>51% of FKBP51 positive tumor cells). On the basis of our analysis, we propose tumor tissue expression of FKBP51 protein as a reliable prognostic marker for OSCC tumors.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Squamous CellCyclin-Dependent Kinase Inhibitor p16FemaleGene ExpressionHuman papillomavirus 16HumansImmunohistochemistryKaplan-Meier EstimateLymphatic MetastasisMaleMiddle AgedMouth NeoplasmsBiomarkers, TumorCyclin-Dependent Kinase Inhibitor p16Tacrolimus Binding Protein 5Tacrolimus Binding ProteinsBayes theoremFKBP51immunotherapyoral cancerprognosissquamous cell carcinoma

Identifiers

PMID28218707
PMCPMC5343977
OpenAlexW2589703425

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.