Evidence map›Paper›PMID 33805080›Full record

ArticleLife (Basel, Switzerland)2021

Expression of Potential Targets for Cell-Based Therapies on Melanoma Cells.

Sophia B Strobel, Devayani Machiraju, Ingrid Hülsmeyer, Jürgen C Becker, Annette Paschen, Dirk Jäger, Winfried S Wels, Michael Bachmann, Jessica C Hassel

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 13 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

9 authors at 3 institutions in 1 country.

Sophia B StrobelDepartment of Dermatology and National Center for Tumor Diseases, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-3127-5643
Devayani MachirajuDepartment of Dermatology and National Center for Tumor Diseases, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Ingrid HülsmeyerGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Jürgen C BeckerGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.ORCID 0000-0001-9183-653X
Annette PaschenGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Dirk JägerNational Center for Tumor Diseases (NCT) Heidelberg, Department of Medical Oncology, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Winfried S WelsGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Michael BachmannHelmholtz-Zentrum Dresden-Rossendorf (HZDR), Institute of Radiopharmaceutical Cancer Research, 01328 Dresden, Germany.ORCID 0000-0002-8029-5755
Jessica C HasselDepartment of Dermatology and National Center for Tumor Diseases, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0001-7575-6230
German Cancer Research Center · DEHeidelberg University · DEGoethe University Frankfurt · DE

Funding

Deutschen Konsortium für Translationale Krebsforschung UniCAR NK cells
6 · The paper itself

Abstract

Tumor antigen-specific redirection of cytotoxic T cells (CTLs) or natural killer (NK) cells including chimeric antigen receptor (CAR-) and T cell receptor (TCR-) cell therapy is currently being evaluated in different tumor entities including melanoma. Expression of melanoma-specific antigen recognized by the respective CAR or TCR directly or presented by HLA molecules is an indispensable prerequisite for this innovative therapy. In this study, we investigated in 168 FFPE tumor specimens of patients with stage I-IV melanoma the protein expression of HER2, TRP2, ABCB5, gp100, p53, and GD2 by immunohistochemistry (IHC). These results were correlated with clinical parameters. Membrane expression of HER2 and GD2 was also investigated in ten melanoma cell lines by flow cytometry for which corresponding tumors were analyzed by IHC. Our results demonstrated that gp100 was the most frequently overexpressed protein (61%), followed by TRP2 (50%), GD2 (38%), p53 (37%), ABCB5 (17%), and HER2 (3%). TRP2 expression was higher in primary tumors compared to metastases (

Indexed as

ABCB5GD2gp100HER2melanomap53targetTRP2

Identifiers

PMID33805080
PMCPMC8064084
OpenAlexW3136153275

What OpenQuestion holds

Textmetadata
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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.