Evidence map›Paper›PMID 29352038›Full record

ArticleBlood2018

Microenvironment-induced CD44v6 promotes early disease progression in chronic lymphocytic leukemia.

Julia C Gutjahr, Eva Szenes, Lisa Tschech, Daniela Asslaber, Michaela Schlederer, Simone Roos, Xiaobing Yu, Tamara Girbl, Christina Sternberg, Alexander Egle and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Recent advances of CAR-T cells in acute myeloid leukemia.Therapeutic advances in hematology · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Leukaemia: a model metastatic disease.Nature reviews. Cancer · 2021
    Review
  10. Review
  11. Article
  12. Article
  13. 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

16 authors at 5 institutions in 4 countries.

Julia C GutjahrThird Medical Department with Hematology, Medical Oncology, Hemostaseology, Infectious Diseases, and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Eva SzenesThird Medical Department with Hematology, Medical Oncology, Hemostaseology, Infectious Diseases, and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Lisa TschechThird Medical Department with Hematology, Medical Oncology, Hemostaseology, Infectious Diseases, and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Daniela AsslaberThird Medical Department with Hematology, Medical Oncology, Hemostaseology, Infectious Diseases, and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Michaela SchledererClinical Institute of Pathology and.
Simone RoosUnit of Pathology of Laboratory Animals, University of Veterinary Medicine, Vienna, Austria.
Xiaobing YuInstitute of Toxicology and Genetics, Karlsruhe Institute of Technology, Karlsruhe, Germany.
Tamara GirblThird Medical Department with Hematology, Medical Oncology, Hemostaseology, Infectious Diseases, and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Christina SternbergCancer Cluster Salzburg, Department of Molecular Biology, Paris-Lodron University of Salzburg, Salzburg, Austria; and.
Alexander EgleThird Medical Department with Hematology, Medical Oncology, Hemostaseology, Infectious Diseases, and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Fritz AbergerCancer Cluster Salzburg, Department of Molecular Biology, Paris-Lodron University of Salzburg, Salzburg, Austria; and.
Ronen AlonDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Lukas KennerClinical Institute of Pathology and.
Richard GreilThird Medical Department with Hematology, Medical Oncology, Hemostaseology, Infectious Diseases, and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Veronique Orian-RousseauInstitute of Toxicology and Genetics, Karlsruhe Institute of Technology, Karlsruhe, Germany.
Tanja N HartmannThird Medical Department with Hematology, Medical Oncology, Hemostaseology, Infectious Diseases, and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.ORCID 0000-0002-2633-7301
Paracelsus Medical University · ATUniversity of Veterinary Medicine Vienna · ATKarlsruhe Institute of Technology · DEUniversity of Salzburg · ATWeizmann Institute of Science · IL

Funding

Austrian Science Fund FWF I 3282
6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) outgrowth depends on signals from the microenvironment. We have previously found that in vitro reconstitution of this microenvironment induces specific variant isoforms of the adhesion molecule CD44, which confer human CLL with high affinity to hyaluronan (HA). Here, we determined the in vivo contribution of standard CD44 and its variants to leukemic B-cell homing and proliferation in Tcl1 transgenic mice with a B-cell-specific CD44 deficiency. In these mice, leukemia onset was delayed and leukemic infiltration of spleen, liver, and lungs, but not of bone marrow, was decreased. Competitive transplantation revealed that CLL homing to spleen and bone marrow required functional CD44. Notably, enrichment of CD44v6 variants particularly in spleen enhanced CLL engraftment and proliferation, along with increased HA binding. We recapitulated CD44v6 induction in the human disease and revealed the involvement of MAPK and NF-κB signaling upon CD40 ligand and B-cell receptor stimulation by in vitro inhibition experiments and chromatin immunoprecipitation assays. The investigation of downstream signaling after CD44v6-HA engagement uncovered the activation of extracellular signal-regulated kinase and p65. Consequently, anti-CD44v6 treatment reduced leukemic cell proliferation in vitro in human and mouse, confirming the general nature of the findings. In summary, we propose a CD44-NF-κB-CD44v6 circuit in CLL, allowing tumor cells to gain HA binding capacity and supporting their proliferation.

Indexed as

Cell ProliferationMAP Kinase Signaling SystemTumor MicroenvironmentAnimalsHumansHyaluronan ReceptorsHyaluronic AcidLeukemia, Lymphocytic, Chronic, B-CellMiceMice, TransgenicNeoplasm ProteinsNF-kappa BReceptors, Antigen, B-CellSpleenCD44 protein, humanCd44 protein, mouseHyaluronan ReceptorsHyaluronic AcidNeoplasm ProteinsNF-kappa BReceptors, Antigen, B-Cell

Identifiers

PMID29352038
PMCPMC5865232
OpenAlexW2783025614

What OpenQuestion holds

Textmetadata
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.