Understanding the molecular pathogenesis of primary central nervous system lymphoma by experimental animal models

Author:

Wu Di1,Liu Dahai1,Tateishi Kensuke2,Qi Fei3,Yang Fang1,Ke Chao4,You Hua5ORCID

Affiliation:

1. Department of Basic Medicine School of Medicine, Foshan University Foshan Guangdong China

2. Department of Neurosurgery Graduate School of Medicine, Yokohama City University Yokohama Japan

3. Department of Pulmonary and Critical Care Medicine Peking University Shenzhen Hospital Shenzhen Guangdong China

4. State Key Laboratory of Oncology in South China, Department of Neurosurgery and Neuro‐oncology Sun Yat‐sen University Cancer Center, Collaborative Innovation Center for Cancer Medicine Guangzhou China

5. Laboratory for Excellence in Systems Biomedicine of Pediatric Oncology, Department of Pediatric Hematology and Oncology, Chongqing Key Laboratory of Pediatrics, Ministry of Education Key Laboratory of Child Development and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, National Clinical Research Center for Child Health and Disorders Children's Hospital of Chongqing Medical University Chongqing China

Abstract

AbstractPrimary central nervous system lymphoma (PCNSL) is a rare and invasive diffuse large B cell lymphoma confined in central nervous system (CNS). The effort to press forward the translational progress has been frustrated by the insufficient understanding of immunophenotype of CNS and tumor genetic alterations of PCNSL, and the lack of validated diagnostic biomarkers. Researchers now have a variety of PCNSL animal models at their disposal that resemble the morphology and immunophenotype of PCNSL, however, a careful and detailed re‐examination of these animal models is needed to clarify the differences in genetic alterations, migration capability, and immune status. In this review, we present the knowledge about the phenotypic and genotypic features of PCNSL tumor cells, and compile the preclinical animal models of PCNSL with regard to various injection sites, cell origins, recipient animals, and immune status, and elaborate on the tropism and migration of tumor cells and novel therapeutic strategies for PCNSL. We envisage that the selection of suitable animal models will serve as a well‐defined preclinical system to understand the molecular pathogenesis of PCNSL, thereby galvanizing the development of novel and potent therapeutic approaches.

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Physiology

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