Evidence map›Paper›PMID 27699266›Full record

ArticleJCI insight2016

Cyclosporine A immunosuppression drives catastrophic squamous cell carcinoma through IL-22.

Melody Abikhair, Hiroshi Mitsui, Valerie Yanofsky, Nazanin Roudiani, Channa Ovits, Teddy Bryan, Tatiana M Oberyszyn, Kathleen L Tober, Juana Gonzalez, James G Krueger and 2 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. The tumor microenvironment of cutaneous squamous cell carcinoma in high-risk patient groups: A scoping review.JID innovations : skin science from molecules to population health · 2026
    Review
  4. Review
  5. Article
  6. The role of IL-22 in cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Chronic UV radiation-induced RORγt+ IL-22-producing lymphoid cells are associated with mutant KC clonal expansion.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. Review
  15. Article
  16. Cutaneous Squamous Cell Carcinoma: From Biology to Therapy.International journal of molecular sciences · 2020
    Review
  17. Article
  18. Review
  19. Article
  20. Article
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

12 authors at 3 institutions in 1 country.

Melody AbikhairRonald O. Perelman Department of Dermatology, New York University (NYU) Langone Medical Center, New York, New York, USA.
Hiroshi MitsuiLaboratory for Investigative Dermatology, Rockefeller University, New York, New York, USA.
Valerie YanofskyRonald O. Perelman Department of Dermatology, New York University (NYU) Langone Medical Center, New York, New York, USA.
Nazanin RoudianiRonald O. Perelman Department of Dermatology, New York University (NYU) Langone Medical Center, New York, New York, USA.
Channa OvitsInstitute for Pediatric Urology, Department of Urology, Weill Cornell Medicine, New York, New York, USA.
Teddy BryanRonald O. Perelman Department of Dermatology, New York University (NYU) Langone Medical Center, New York, New York, USA.
Tatiana M OberyszynDepartment of Pathology, The Ohio State University, Columbus, Ohio, USA.
Kathleen L ToberDepartment of Pathology, The Ohio State University, Columbus, Ohio, USA.
Juana GonzalezTranslational Immunomonitoring Resource Center, Rockefeller University, New York, New York, USA.
James G KruegerLaboratory for Investigative Dermatology, Rockefeller University, New York, New York, USA.
Diane FelsenInstitute for Pediatric Urology, Department of Urology, Weill Cornell Medicine, New York, New York, USA.
John A CarucciRonald O. Perelman Department of Dermatology, New York University (NYU) Langone Medical Center, New York, New York, USA.
Rockefeller University · USThe Ohio State University · USWeill Cornell Medicine · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
NCI NIH HHS P30 CA016058NCI NIH HHS P30 CA016087
6 · The paper itself

Abstract

Immune-suppressed organ transplant recipients (OTRs) can develop catastrophic squamous cell carcinoma (SCC), characterized by multiple primary tumors, extensive body surface area involvement, or metastases. There are currently no curative systemic therapies available. We previously showed that IL-22 enhances SCC proliferation. Herein, we examined links between cyclosporine (CSA), IL-22, and SCC in patients, cell lines, and mice with UV light-induced SCC. Eighteen of 114 OTRs developed catastrophic SCC, which was strongly associated with CSA treatment. We found that CSA drives T cell polarization toward IL-22-producing T22 cells, and CSA treatment increased IL-22 receptor in SCC cells. SCC tissue from OTRs showed increased expression of IL-22RA1. CSA potentiated rescue by IL-22 of serum-starved SCC cells; treatment of SCC cells with IL-22 and CSA increased both their migratory and invasive capacity. In a UV-induced model of SCC in SKH-1 immunocompetent mice, treatment with anti-IL-22 antibody reduced tumor number and tumor burden. We found that catastrophic SCC in OTRs is associated with CSA use, which may be acting by favoring T22 polarization. Since anti-IL-22 antibody administration decreased tumor number and tumor burden in vivo, blockade of the IL-22 axis may be developed as a viable therapeutic option for catastrophic SCC.

Indexed as

AnimalsCarcinoma, Squamous CellCell Line, TumorCyclosporineHumansImmunosuppressive AgentsInterleukin-22InterleukinsMiceReceptors, InterleukinSkin NeoplasmsCyclosporineImmunosuppressive AgentsInterleukin-22interleukin-22 receptorInterleukinsReceptors, Interleukin

Identifiers

PMID27699266
PMCPMC5033893
OpenAlexW2415684512

What OpenQuestion holds

Textmetadata
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.