Evidence map›Paper›PMID 28829805›Full record

ArticlePloS one2017

Expression of IL-23/Th17-related cytokines in basal cell carcinoma and in the response to medical treatments.

Cristina Pellegrini, Augusto Orlandi, Gaetana Costanza, Alessandro Di Stefani, Antonella Piccioni, Antonella Di Cesare, Andrea Chiricozzi, Amedeo Ferlosio, Ketty Peris, Maria Concetta Fargnoli

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Immunotherapy in Basal Cell Carcinoma.Journal of clinical medicine · 2024
    Review
  6. The role of IL-22 in cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Relationship between Th17 immune response and cancer.World journal of clinical oncology · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. 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

10 authors at 4 institutions in 1 country.

Cristina PellegriniBiotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Augusto OrlandiDepartment of Biomedicine and Prevention, Anatomic Pathology, University of Rome Tor Vergata, Rome, Italy.
Gaetana CostanzaDepartment of Biomedicine and Prevention, Anatomic Pathology, University of Rome Tor Vergata, Rome, Italy.
Alessandro Di StefaniInstitute of Dermatology, Catholic University, Rome, Italy.
Antonella PiccioniBiotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Antonella Di CesareDivision of Clinical, Preventive and Oncologic Dermatology, Department of Surgery and Translational Medicine, University of Florence, Florence, Italy.
Andrea ChiricozziDermatology Department, University of Pisa, Pisa, Italy.
Amedeo FerlosioDepartment of Biomedicine and Prevention, Anatomic Pathology, University of Rome Tor Vergata, Rome, Italy.
Ketty PerisInstitute of Dermatology, Catholic University, Rome, Italy.
Maria Concetta FargnoliBiotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.ORCID http://orcid.org/0000-0002-7249-2556
University of L'Aquila · ITUniversity of Rome Tor Vergata · ITUniversity of Florence · ITUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several immune-related markers have been implicated in basal cell carcinoma (BCC) pathogenesis. The BCC inflammatory infiltrate is dominated by Th2 cytokines, suggesting a specific state of immunosuppression. In contrast, regressing BCC are characterized by a Th1 immune response with IFN-γ promoting a tumor suppressive activity. IL-23/Th17-related cytokines, as interleukin (IL)-17, IL-23 and IL-22, play a significant role in cutaneous inflammatory diseases, but their involvement in skin carcinogenesis is controversial and is poorly investigated in BCC. In this study we investigated the expression of IFN-γ, IL-17, IL-23 and IL-22 cytokines in BCC at the protein and mRNA level and their modulation during imiquimod (IMQ) treatment or photodynamic therapy (PDT). IFN-γ, IL-17, IL-23 and IL-22 levels were evaluated by immunohistochemistry and quantitative Real Time PCR in 41 histopathologically-proven BCCs (28 superficial and 13 nodular) from 39 patients. All BCC samples were analyzed at baseline and 19 of 41 also during medical treatment (9 with IMQ 5% cream and 10 with MAL-PDT). Association between cytokines expression and clinico-pathological variables was evaluated. Higher levels of IFN-γ, IL-17, IL-23 and IL-22 were found in BCCs, mainly in the peritumoral infiltrate, compared to normal skin, with the expression being correlated to the severity of the inflammatory infiltrate. IFN-γ production was higher in superficial BCCs compared to nodular BCCs, while IL-17 was increased in nodular BCCs. A significant correlation was found between IFN-γ and IL-17 expression with both cytokines expressed by CD4+ and CD8+ T-cells. An increase of all cytokines occurred during the inflammatory phase induced by IMQ and at the early time point of PDT treatment, with significant evidence for IFN-γ, IL-23, and IL-22. Our results confirm the role of IFN-γ and support the involvement of IL-23/Th17-related cytokines in BCC pathogenesis and in the inflammatory response during IMQ and MAL-PDT treatments.

Indexed as

AdultAgedAged, 80 and overAminoquinolinesAntineoplastic AgentsBasal Cell CarcinomaCytokinesFemaleHumansImiquimodInterleukin-23MaleMiddle AgedPhotochemotherapyReal-Time Polymerase Chain ReactionRNA, MessengerAminoquinolinesAntineoplastic AgentsCytokinesImiquimodInterleukin-23RNA, Messenger

Identifiers

PMID28829805
PMCPMC5567915
OpenAlexW2749640902

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.