Evidence map›Paper›PMID 35740600›Full record

ArticleCancers2022

ALK+ Anaplastic Large Cell Lymphoma (ALCL)-Derived Exosomes Carry ALK Signaling Proteins and Interact with Tumor Microenvironment.

Dimitrios Chioureas, Janina Beck, George Baltatzis, Ioulia Vardaki, Pedro Fonseca, Nikolaos Tsesmetzis, Francisco Vega, Vasiliki Leventaki, Aristides G Eliopoulos, Elias Drakos and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. 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

12 authors at 6 institutions in 3 countries.

Dimitrios ChioureasDepartment of Oncology and Pathology, Karolinska Institutet, SE-17176 Stockholm, Sweden.
Janina BeckDepartment of Oncology and Pathology, Karolinska Institutet, SE-17176 Stockholm, Sweden.
George BaltatzisDepartment of Oncology and Pathology, Karolinska Institutet, SE-17176 Stockholm, Sweden.
Ioulia VardakiDepartment of Oncology and Pathology, Karolinska Institutet, SE-17176 Stockholm, Sweden.
Pedro FonsecaDepartment of Oncology and Pathology, Karolinska Institutet, SE-17176 Stockholm, Sweden.
Nikolaos TsesmetzisDepartment of Oncology and Pathology, Karolinska Institutet, SE-17176 Stockholm, Sweden.
Francisco VegaDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0001-5956-452X
Vasiliki LeventakiDepartment of Pathology, Children's Hospital of Wisconsin & Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Aristides G EliopoulosDepartment of Biology, School of Medicine, National and Kapodistrian University of Athens, 115 27 Athens, Greece.ORCID 0000-0002-6403-6761
Elias DrakosDepartment of Pathology, University of Crete Medical School, 715 00 Heraklion, Greece.
George Z RassidakisDepartment of Oncology and Pathology, Karolinska Institutet, SE-17176 Stockholm, Sweden.
Theocharis PanaretakisDepartment of Oncology and Pathology, Karolinska Institutet, SE-17176 Stockholm, Sweden.ORCID 0000-0001-5754-6950
Karolinska Institutet · SEThe University of Texas MD Anderson Cancer Center · USChildren's Hospital of Wisconsin · USKarolinska University Hospital · SENational and Kapodistrian University of Athens · GRUniversity of Crete · GR

Funding

Radiumhemmets Research Foundation, King Gustaf V Jubilee Fund 204133Swedish Cancer Society 19 0277 PJSwedish Childhood Cancer Fund PR2021-0113
6 · The paper itself

Abstract

The oncogenic pathways activated by the NPM-ALK chimeric kinase of ALK+ anaplastic large cell lymphoma (ALCL) are well characterized; however, the potential interactions of ALK signaling with the microenvironment are not yet known. Here we report that ALK+ ALCL-derived exosomes contain critical components of ALK signaling as well as CD30, and that exosome uptake by lymphoid cells led to increased proliferation and expression of critical antiapoptotic proteins by the recipient cells. The bone marrow fibroblasts highly uptake ALK+ ALCL-derived exosomes and acquire a cancer-associated fibroblast (CAF) phenotype. Moreover, exosome-mediated activation of stromal cells altered the cytokine profile of the microenvironment. These interactions may contribute to tumor aggressiveness and possibly resistance to treatment.

Indexed as

cytokinesexosomeslymphomamicroenvironmentNPM-ALK

Identifiers

PMID35740600
PMCPMC9221431
OpenAlexW4282921030

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.