Evidence map›Paper›PMID 33767253›Full record

ArticleScientific reports2021

SPINK7 expression changes accompanied by HER2, P53 and RB1 can be relevant in predicting oral squamous cell carcinoma at a molecular level.

Gina Pennacchiotti, Fabio Valdés-Gutiérrez, Wilfredo Alejandro González-Arriagada, Héctor Federico Montes, Judith Maria Roxana Parra, Valeria Andrea Guida, Silvina Esther Gómez, Martin Eduardo Guerrero-Gimenez, Juan Manuel Fernandez-Muñoz, Felipe Carlos Martin Zoppino and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Inflammation in Penile Squamous Cell Carcinoma: A Comprehensive Review.International journal of molecular sciences · 2025
    Review
  4. Article
  5. ECRG2/SPINK7 Tumor Suppressor as Modulator of DNA Damage Response.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

14 authors at 9 institutions in 2 countries.

Gina PennacchiottiArea Medicina Oral Departamento de Patología Facultad de Odontología, Universidad de Chile, Av. Olivos 243, Independencia, Región Metropolitana, CP8320000, Santiago, Chile.
Fabio Valdés-GutiérrezInstituto Nacional del Cáncer, Av. Profesor Zañartu 1010, Independencia, Región Metropolitana, CP8320000, Santiago, Chile.
Wilfredo Alejandro González-ArriagadaCIICOM, Facultad de Odontología, Universidad de Valparaíso, Subida Carvallo 211, Playa ancha, CP2390302, Valparaíso, Chile.
Héctor Federico MontesDepartamento de Cirugía Cabeza-Cuello Clínica Montes, Ituzaingo 1446, CP5500, Capital, Mendoza, Argentina.
Judith Maria Roxana ParraServicio de Medicina Bucal (SEMEB), Facultad de Odontología, Universidad Nacional de Cuyo (FOdonto-UNCuyo), Centro Universitario, CP5500, Mendoza Capital, Argentina.
Valeria Andrea GuidaServicio de Medicina Bucal (SEMEB), Facultad de Odontología, Universidad Nacional de Cuyo (FOdonto-UNCuyo), Centro Universitario, CP5500, Mendoza Capital, Argentina.
Silvina Esther GómezInstituto de Medicina y Biología Experimental de Cuyo (IMBECU) CCT-Mendoza CONICET, Universidad Nacional de Cuyo (UNCuyo). Av. Adrián Ruiz Leal W/N, CP5500, Capital, Mendoza, Argentina.
Martin Eduardo Guerrero-GimenezInstituto de Medicina y Biología Experimental de Cuyo (IMBECU) CCT-Mendoza CONICET, Universidad Nacional de Cuyo (UNCuyo). Av. Adrián Ruiz Leal W/N, CP5500, Capital, Mendoza, Argentina.
Juan Manuel Fernandez-MuñozInstituto de Medicina y Biología Experimental de Cuyo (IMBECU) CCT-Mendoza CONICET, Universidad Nacional de Cuyo (UNCuyo). Av. Adrián Ruiz Leal W/N, CP5500, Capital, Mendoza, Argentina.
Felipe Carlos Martin ZoppinoInstituto de Medicina y Biología Experimental de Cuyo (IMBECU) CCT-Mendoza CONICET, Universidad Nacional de Cuyo (UNCuyo). Av. Adrián Ruiz Leal W/N, CP5500, Capital, Mendoza, Argentina.
Rubén Walter CarónInstituto de Medicina y Biología Experimental de Cuyo (IMBECU) CCT-Mendoza CONICET, Universidad Nacional de Cuyo (UNCuyo). Av. Adrián Ruiz Leal W/N, CP5500, Capital, Mendoza, Argentina.
Marcelo Eduardo EzquerCentro de Medicina Regenerativa, Facultad de Medicina, Universidad del Desarrollo-Clínica Alemana (FM, UDD-CAS), Av Las Condes 12.438, CP7690000, Lo Barnechea. Santiago, Chile.
Ricardo Fernández-RamiresEscuela de Odontología, Facultad de Ciencias, Universidad Mayor (UMayor), Avda Libertador Bernardo O`Higgins 2013. Región Metropolitana, CP8320000, Santiago, Chile.
Flavia Alejandra BrunaServicio de Medicina Bucal (SEMEB), Facultad de Odontología, Universidad Nacional de Cuyo (FOdonto-UNCuyo), Centro Universitario, CP5500, Mendoza Capital, Argentina. flabruna@gmail.com.
Consejo Nacional de Investigaciones Científicas y Técnicas · ARInstituto de Medicina y Biología Experimental de Cuyo · ARUniversidad Nacional de Cuyo · ARClínica Alemana · CLInstituto Nacional del Cáncer · CLUniversidad del Desarrollo · CLUniversidad Mayor · CLUniversity of Chile · CLUniversity of Valparaíso · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The oral squamous cell carcinoma (OSCC), which has a high morbidity rate, affects patients worldwide. Changes in SPINK7 in precancerous lesions could promote oncogenesis. Our aim was to evaluate SPINK7 as a potential molecular biomarker which predicts OSCC stages, compared to: HER2, TP53, RB1, NFKB and CYP4B1. This study used oral biopsies from three patient groups: dysplasia (n = 33), less invasive (n = 28) and highly invasive OSCC (n = 18). The control group consisted of clinically suspicious cases later to be confirmed as normal mucosa (n = 20). Gene levels of SPINK7, P53, RB, NFKB and CYP4B1 were quantified by qPCR. SPINK7 levels were correlated with a cohort of 330 patients from the TCGA. Also, SPINK7, HER2, TP53, and RB1, were evaluated by immunohistofluorescence. One-way Kruskal-Wallis test and Dunn's post-hoc with a p < 0.05 significance was used to analyze data. In OSCC, the SPINK7 expression had down regulated while P53, RB, NFKB and CYP4B1 had up regulated (p < 0.001). SPINK7 had also diminished in TCGA patients (p = 2.10e-6). In less invasive OSCC, SPINK7 and HER2 proteins had decreased while TP53 and RB1 had increased with respect to the other groups (p < 0.05). The changes of SPINK7 accompanied by HER2, P53 and RB1 can be used to classify the molecular stage of OSCC lesions allowing a diagnosis at molecular and histopathological levels.

Indexed as

AdultBiomarkers, TumorCarcinoma, Squamous CellCase-Control StudiesErb-b2 Receptor Tyrosine KinasesFemaleHumansMaleMiddle AgedMouth NeoplasmsRetinoblastoma Binding ProteinsSerine Peptidase Inhibitors, Kazal TypeTumor Suppressor Protein p53Ubiquitin-Protein LigasesBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesRB1 protein, humanRetinoblastoma Binding ProteinsSerine Peptidase Inhibitors, Kazal TypeSPINK7 protein, humanTumor Suppressor Protein p53Ubiquitin-Protein Ligases

Identifiers

PMID33767253
PMCPMC7994578
OpenAlexW3138295256

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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.