T‐cell‐derived Hodgkin lymphoma has motility characteristics intermediate between Hodgkin and anaplastic large cell lymphoma-Reference-Cited by-同舟云学术

T‐cell‐derived Hodgkin lymphoma has motility characteristics intermediate between Hodgkin and anaplastic large cell lymphoma

Published:2022-05-19 Issue:12 Volume:26 Page:3495-3505
ISSN:1582-1838
Container-title:Journal of Cellular and Molecular Medicine
language:en
Short-container-title:J Cellular Molecular Medi

Author:

Bein Julia¹,Flinner Nadine¹²³⁴,Häupl Björn²⁵⁶,Mathur Aastha⁷,Schneider Olga¹,Abu‐Ayyad Marwa¹,Hansmann Martin‐Leo⁴⁸,Piel Matthieu⁷,Oellerich Thomas²⁵⁶,Hartmann Sylvia¹^ORCID

Affiliation:

1. Dr. Senckenberg Institute of Pathology Goethe University Frankfurt am Main Frankfurt am Main Germany

2. Frankfurt Cancer Institute Goethe University Frankfurt am Main Germany

3. University Cancer Center (UCT) Frankfurt University Hospital Goethe University Frankfurt am Main Germany

4. Frankfurt Institute for Advanced Studies Frankfurt am Main Germany

5. Department of Internal Medicine 2 Goethe University Hospital Frankfurt Germany

6. German Cancer Consortium/German Cancer Research Center Heidelberg Germany

7. Institut Curie and Institut Pierre Gilles de Gennes PSL Research University CNRS UMR 144 Paris France

8. Institute of General Pharmacology and Toxicology Goethe University Frankfurt am Main Frankfurt am Main Germany

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jcmm.17389

Reference36 articles.

1. The nature of Hodgkin and Reed-Sternberg cells, their association with EBV, and their relationship to anaplastic large-cell lymphoma

2. Incidence Patterns and Outcomes for Hodgkin Lymphoma Patients in the United States

3. Anaplastic large cell lymphoma, ALK-positive

4. Loss of the B-lineage–specific gene expression program in Hodgkin and Reed-Sternberg cells of Hodgkin lymphoma

5. Anaplastic large cell lymphomas lack the expression of T-cell receptor molecules or molecules of proximal T-cell receptor signaling

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