Evidence map›Paper›PMID 32528281›Full record

ArticleFrontiers in pharmacology2020

A Novel Anti-Kv10.1 Nanobody Fused to Single-Chain TRAIL Enhances Apoptosis Induction in Cancer Cells.

Franziska Hartung, Thomas Krüwel, Xiaoyi Shi, Klaus Pfizenmaier, Roland Kontermann, Patrick Chames, Frauke Alves, Luis A Pardo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  6. Article
  7. Modulating ion channels with nanobodies.Synthetic and systems biotechnology · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. The Kv10.1 Channel: A Promising Target in Cancer.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Potassium and Chloride Ion Channels in Cancer: A Novel Paradigm for Cancer Therapeutics.Reviews of physiology, biochemistry and pharmacology · 2022
    Review
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

8 authors at 4 institutions in 2 countries.

Franziska HartungOncophysiology Group, Max Planck, Institute of Experimental Medicine, Göttingen, Germany.
Thomas KrüwelInstitute of Diagnostic and Interventional Radiology, University Medical Center Göttingen, Göttingen, Germany.
Xiaoyi ShiOncophysiology Group, Max Planck, Institute of Experimental Medicine, Göttingen, Germany.
Klaus PfizenmaierInstitut für Zellbiologie und Immunologie, Universität Stuttgart, Stuttgart, Germany.
Roland KontermannInstitut für Zellbiologie und Immunologie, Universität Stuttgart, Stuttgart, Germany.
Patrick ChamesAix Marseille Univ, CNRS, Inserm, Institut Paoli-Calmettes, CRCM, Marseille, France.
Frauke AlvesInstitute of Diagnostic and Interventional Radiology, University Medical Center Göttingen, Göttingen, Germany.
Luis A PardoOncophysiology Group, Max Planck, Institute of Experimental Medicine, Göttingen, Germany.
Max Planck Institute of Experimental Medicine · DEUniversitätsmedizin Göttingen · DEUniversity of Stuttgart · DECentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibody-based therapies hold promise for a safe and efficient treatment of cancer. The identification of target tumor cells through a specific antigen enriched on their surface and the subsequent delivery of the therapeutic agent only to those cells requires, besides the efficacy of the therapeutic agent itself, the identification of an antigen enriched on the surface of tumor cells, the generation of high affinity antibodies against that antigen. We have generated single-domain antibodies (nanobodies) against the voltage-gated potassium channel Kv10.1, which outside of the brain is detectable almost exclusively in tumor cells. The nanobody with highest affinity was fused to an improved form of the tumor necrosis factor-related apoptosis inducing ligand TRAIL, to target this cytokine to the surface of tumor cells. The resulting construct, VHH-D9-scTRAIL, shows rapid and strong apoptosis induction in different tumor models in cell culture. The construct combines two sources of specificity, the expression of the antigen restricted to tumor cells and the tumor selectivity of TRAIL. Such specificity combined with the high affinity obtained through nanobodies make the novel agent a promising concept for cancer therapy.

Indexed as

apoptosisKv10.1nanobodytargeted therapyTRAILvoltage-gated potassium channel

Identifiers

PMID32528281
PMCPMC7246340
OpenAlexW3024093412

What OpenQuestion holds

Textmetadata
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.