Evidence map›Paper›PMID 34360654›Full record

ArticleInternational journal of molecular sciences2021

CD147-Cyclophilin a Interactions Promote Proliferation and Survival of Cutaneous T-Cell Lymphoma.

Minami Sakamoto, Tomomitsu Miyagaki, Hiroaki Kamijo, Tomonori Oka, Hikari Boki, Naomi Takahashi-Shishido, Hiraku Suga, Makoto Sugaya, Shinichi Sato

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

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  12. Review
  13. Cyclophilin A/CD147 Interaction: A Promising Target for Anticancer Therapy.International journal of molecular sciences · 2022
    Review
  14. 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

9 authors at 2 institutions in 1 country.

Minami SakamotoDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.
Tomomitsu MiyagakiDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.ORCID 0000-0003-1879-3128
Hiroaki KamijoDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.
Tomonori OkaDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.ORCID 0000-0001-7362-3207
Hikari BokiDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.
Naomi Takahashi-ShishidoDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.
Hiraku SugaDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.
Makoto SugayaDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.
Shinichi SatoDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.
The University of Tokyo · JPSt. Marianna University School of Medicine · JP

Funding

Ministry of Education, Culture, Sports, Science and Technology 16K19709Ministry of Education, Culture, Sports, Science and Technology 26893052
6 · The paper itself

Abstract

CD147, a transmembrane glycoprotein that belongs to the immunoglobulin superfamily, and cyclophilin A (CypA), one of the binding partners of CD147, are overexpressed in tumor cells and associated with the progression of several malignancies, including both solid and hematological malignancies. However, CD147 and CypA involvement in cutaneous T-cell lymphoma (CTCL) has not been reported. In this study, we examined CD147 and CypA expression and function using clinical samples of mycosis fungoides (MF) and Sézary syndrome (SS) and CTCL cell lines. CD147 and CypA were overexpressed by tumor cells of MF/SS, and CypA was also expressed by epidermal keratinocytes in MF/SS lesional skin. Serum CypA levels were increased and correlated with disease severity markers in MF/SS patients. Anti-CD147 antibody and/or anti-CypA antibody suppressed the proliferation of CTCL cell lines, both in vitro and in vivo, via downregulation of phosphorylated extracellular-regulated kinase 1/2 and Akt. These results suggest that CD147-CypA interactions can contribute to the proliferation of MF/SS tumor cells in both a autocrine and paracrine manner, and that the disruption of CD147-CypA interactions could be a new therapeutic strategy for the treatment of MF/SS.

Indexed as

Cell ProliferationBasiginCase-Control StudiesCyclophilin AFemaleHumansLymphoma, T-Cell, CutaneousMaleMiddle AgedMycosis FungoidesSeverity of Illness IndexSezary SyndromeSkin NeoplasmsBasiginBSG protein, humanCyclophilin ACD147cutaneous T-cell lymphomacyclophilin Amycosis fungoidesSézary syndrome

Identifiers

PMID34360654
PMCPMC8346093
OpenAlexW3185905421

What OpenQuestion holds

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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.