Evidence map›Paper›PMID 39840532›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

Peptide-Drug Conjugate for Therapeutic Reprogramming of Tumor-Associated Macrophages in Breast Cancer.

Anni Lepland, Elisa Peranzoni, Uku Haljasorg, Eliana K Asciutto, Maria Crespí-Amer, Lorenzo Modesti, Kalle Kilk, Manuel Lombardia, Gerardo Acosta, Miriam Royo and 4 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Review
  4. DCC-2036 induces repolarization of TAMs to M1 type and enhances CD8Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. 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

14 authors.

Anni LeplandInstitute of Biomedicine and Translational Medicine, University of Tartu, Ravila 14B, Tartu, 50411, Estonia.
Elisa PeranzoniImmunology and Molecular Oncology Diagnostics, Veneto Institute of Oncology IOV - IRCCS, Padua, 35128, Italy.
Uku HaljasorgMolecular Pathology Research Group, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, 50411, Estonia.
Eliana K AsciuttoInstituto de Ciencias Físicas, Universidad Nacional de San Martin (UNSAM) and CONICET, Campus Migueletes, 25 de Mayo y Francia, Buenos Aires, CP 1650, Argentina.
Maria Crespí-AmerInstitute for Advanced Chemistry of Catalonia, IQAC-CSIC, Jordi Girona 18-26, Barcelona, 08034, Spain.
Lorenzo ModestiImmunology and Molecular Oncology Diagnostics, Veneto Institute of Oncology IOV - IRCCS, Padua, 35128, Italy.
Kalle KilkDepartment of biochemistry, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, Tartu, 50411, Estonia.
Manuel LombardiaProteomics core facility, Centro Nacional de Biotecnologia, CNB-CSIC, Calle Darwin 3, Madrid, 28049, Spain.
Gerardo AcostaInstitute for Advanced Chemistry of Catalonia, IQAC-CSIC, Jordi Girona 18-26, Barcelona, 08034, Spain.
Miriam RoyoInstitute for Advanced Chemistry of Catalonia, IQAC-CSIC, Jordi Girona 18-26, Barcelona, 08034, Spain.
Pärt PetersonMolecular Pathology Research Group, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, 50411, Estonia.
Ilaria MarigoImmunology and Molecular Oncology Diagnostics, Veneto Institute of Oncology IOV - IRCCS, Padua, 35128, Italy.
Tambet TeesaluInstitute of Biomedicine and Translational Medicine, University of Tartu, Ravila 14B, Tartu, 50411, Estonia.
Pablo ScodellerInstitute of Biomedicine and Translational Medicine, University of Tartu, Ravila 14B, Tartu, 50411, Estonia.ORCID https://orcid.org/0000-0003-0745-2467

Funding

CIBER BBN CB06/01/0074"ERDF A way of making Europe" PID2021-122364OA-I00Estonian Research Agency PRG2011Estonian Research Council PRG1788Estonian Research Council PRG230Estonian Research Council PSG38MICIN/AEIMCIN/AEI /10.13039/501100011033/MSCA-RISE 2018 Project OXIGENATED, and EuronanomedIIIRamon y Cajal RYC2020-028754-IRoyal Society of Chemistry R21-6405053838Università di Padova DiSCOG MARI_BIRD22_01
6 · The paper itself

Abstract

In triple-negative breast cancer (TNBC), pro-tumoral macrophages promote metastasis and suppress the immune response. To target these cells, a previously identified CD206 (mannose receptor)-binding peptide, mUNO was engineered to enhance its affinity and proteolytic stability. The new rationally designed peptide, MACTIDE, includes a trypsin inhibitor loop, from the Sunflower Trypsin Inhibitor-I. Binding studies to recombinant CD206 revealed a 15-fold lower K

Indexed as

PeptidesTriple Negative Breast NeoplasmsTumor-Associated MacrophagesAnimalsCell Line, TumorFemaleHumansMannose ReceptorMiceMannose ReceptorPeptidesCD206peptide‐drug conjugatetargeting peptidestriple negative breast cancertumor‐associated macrophages

Identifiers

PMID39840532
PMCPMC11904948

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.