Evidence map›Paper›PMID 39605056›Full record

ArticleCell communication and signaling : CCS2024

A novel process for transcellular hemoglobin transport from macrophages to cancer cells.

Agata Braniewska, Marcin Skorzynski, Zuzanna Sas, Magdalena Dlugolecka, Ilona Marszalek, Daria Kurpiel, Marcel Bühler, Damian Strzemecki, Aneta Magiera, Maciej Bialasek and 9 more

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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

19 authors.

Agata BraniewskaDepartment of Immunology, Mossakowski Medical Research Institute, Polish Academy of Sciences, 02-106, Warsaw, Poland.
Marcin SkorzynskiDepartment of Immunology, Mossakowski Medical Research Institute, Polish Academy of Sciences, 02-106, Warsaw, Poland.
Zuzanna SasDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Magdalena DlugoleckaChair and Department of Biochemistry, Doctoral School, Medical University of Warsaw, Warsaw, Poland.
Ilona MarszalekCellis AG, Zurich, Switzerland.
Daria KurpielCellis AG, Zurich, Switzerland.
Marcel BühlerLaboratory of Molecular Neuro-Oncology, Department of Neurology, Clinical Neuroscience Center, University Hospital and University of Zurich, Zurich, Switzerland.
Damian StrzemeckiCellis AG, Zurich, Switzerland.
Aneta MagieraInstitute of Physical Chemistry, Polish Academy of Sciences, Warsaw, Poland.
Maciej BialasekCellis AG, Zurich, Switzerland.
Jaroslaw WalczakInstitute of Fundamental Technological Research, Polish Academy of Sciences, Warsaw, Poland.
Lukasz ChedaFaculty of Chemistry, University of Warsaw, Warsaw, Poland.
Michal KomorowskiInstitute of Fundamental Technological Research, Polish Academy of Sciences, Warsaw, Poland.
Tobias WeissLaboratory of Molecular Neuro-Oncology, Department of Neurology, Clinical Neuroscience Center, University Hospital and University of Zurich, Zurich, Switzerland.
Małgorzata Czystowska-KuzmiczChair and Department of Biochemistry, Medical University of Warsaw, Warsaw, Poland.
Karina KwapiszewskaInstitute of Physical Chemistry, Polish Academy of Sciences, Warsaw, Poland.
Alberto BoffiCellis AG, Zurich, Switzerland.
Magdalena KrolCellis AG, Zurich, Switzerland.
Tomasz P RygielDepartment of Immunology, Mossakowski Medical Research Institute, Polish Academy of Sciences, 02-106, Warsaw, Poland. trygiel@imdik.pan.pl.

Funding

Fundacja na rzecz Nauki Polskiej TEAM TECH /2016-1/8Ministry of Science and Higher Education, Poland DIALOG-0188/DLG/2018/10Narodowe Centrum Nauki 2019/35/N/ST4/01987National Center for Gene Therapy and Drugs based on RNA Technology CN 00000041
6 · The paper itself

Abstract

Hemoglobin (Hb) performs its physiological function within the erythrocyte. Extracellular Hb has prooxidative and proinflammatory properties and is therefore sequestered by haptoglobin and bound by the CD163 receptor on macrophages. In the present study, we demonstrate a novel process of Hb uptake by macrophages independent of haptoglobin and CD163. Unexpectedly, macrophages do not degrade the entire Hb, but instead transfer it to neighboring cells. We have shown that the phenomenon of Hb transfer from macrophages to other cells is mainly mediated by extracellular vesicles. In contrast to the canonical Hb degradation pathway by macrophages, Hb transfer has not been reported before. In addition, we have used the process of Hb transfer in anticancer therapy, where macrophages are loaded with a Hb-anticancer drug conjugate and act as cellular drug carriers. Both mouse and human macrophages loaded with Hb-monomethyl auristatin E (MMAE) effectively killed cancer cells when co-cultured in vitro.

Indexed as

HemoglobinsMacrophagesAnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticBiological TransportCD163 AntigenCell Line, TumorExtracellular VesiclesHaptoglobinsHumansMiceNeoplasmsOligopeptidesRAW 264.7 CellsReceptors, Cell SurfaceAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenHaptoglobinsHemoglobinsOligopeptidesReceptors, Cell SurfaceCD163Extracellular vesiclesHemoglobinMacrophagesMonomethyl auristatin E

Identifiers

PMID39605056
PMCPMC11603754

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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.