Evidence map›Paper›PMID 34359687›Full record

ArticleCancers2021

Cyclic Derivatives of the Chemerin C-Terminus as Metabolically Stable Agonists at the Chemokine-like Receptor 1 for Cancer Treatment.

Tobias F Fischer, Anne S Czerniak, Tina Weiß, Tristan Zellmann, Lina Zielke, Sylvia Els-Heindl, Annette G Beck-Sickinger

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Research advances in peptide‒drug conjugates.Acta pharmaceutica Sinica. B · 2023
    Review
  8. Article
  9. Enzyme-Activatable Chemokine Conjugates for In Vivo Targeting of Tumor-Associated Macrophages.Angewandte Chemie (Weinheim an der Bergstrasse, Germany) · 2022
    Article
  10. Review
  11. 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

7 authors at 1 institution in 1 country.

Tobias F FischerInstitute of Biochemistry, Leipzig University, Brüderstraße 34, 04103 Leipzig, Germany.
Anne S CzerniakInstitute of Biochemistry, Leipzig University, Brüderstraße 34, 04103 Leipzig, Germany.ORCID 0000-0003-3269-1216
Tina WeißInstitute of Biochemistry, Leipzig University, Brüderstraße 34, 04103 Leipzig, Germany.
Tristan ZellmannInstitute of Biochemistry, Leipzig University, Brüderstraße 34, 04103 Leipzig, Germany.
Lina ZielkeInstitute of Biochemistry, Leipzig University, Brüderstraße 34, 04103 Leipzig, Germany.ORCID 0000-0001-8257-4355
Sylvia Els-HeindlInstitute of Biochemistry, Leipzig University, Brüderstraße 34, 04103 Leipzig, Germany.
Annette G Beck-SickingerInstitute of Biochemistry, Leipzig University, Brüderstraße 34, 04103 Leipzig, Germany.
Leipzig University · DE

Funding

Deutsche Forschungsgemeinschaft SFB 1052
6 · The paper itself

Abstract

Chemerin is a small chemotactic protein and a modulator of the innate immune system. Its activity is mainly mediated by the chemokine-like receptor 1 (CMKLR1), a receptor expressed by natural killer cells, dendritic cells, and macrophages. Downregulation of chemerin is part of the immune evasion strategy exploited by several cancer types, including melanoma, breast cancer, and hepatocellular carcinoma. Administration of chemerin can potentially counteract these effects, but synthetically accessible, metabolically stable analogs are required. Other tumors display overexpression of CMKLR1, offering a potential entry point for targeted delivery of chemotherapeutics. Here, we present cyclic derivatives of the chemerin C-terminus (chemerin-9), the minimal activation sequence of chemerin. Chemerin-9 derivatives that were cyclized through positions four and nine retained activity while displaying full stability in blood plasma for more than 24 h. Therefore, these peptides could be used as a drug shuttle system to target cancer cells as demonstrated here by methotrexate conjugates.

Indexed as

chemerinCMKLR1GPCRpeptide–drug conjugatespeptides

Identifiers

PMID34359687
PMCPMC8345219
OpenAlexW3183990284

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.