Literature DB >> 34893151

Genetic predisposition to lymphomas: Overview of rare syndromes and inherited familial variants.

Bartosz Szmyd1, Wojciech Mlynarski2, Agata Pastorczak3.   

Abstract

Approximately 10 % of malignancies occur in carriers of germline mutations predisposing to cancer. A high risk of developing lymphomas has been noted in many primary immunodeficiencies, including DNA repair disorders. Moreover, implementation of next-generation sequencing has recently enabled to uncover rare genetic variants predisposing patients to lymphoid neoplasms. Some patients harboring inherited predisposition to lymphomas require dedicated clinical management, which will contribute to effective cancer treatment and to the prevention of potential severe toxicities and secondary malignancies. In line with that, our review summarizes the natural history of lymphoid tumors developing on different germline genetic backgrounds and discusses the progress that has been made toward successfully treating these malignancies.
Copyright © 2021 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Genetic predisposition; Genetic syndromes; Germline variants; Lymphoma

Mesh:

Year:  2021        PMID: 34893151     DOI: 10.1016/j.mrrev.2021.108386

Source DB:  PubMed          Journal:  Mutat Res Rev Mutat Res        ISSN: 1383-5742            Impact factor:   5.657


  2 in total

Review 1.  Genetic Disorders with Predisposition to Paediatric Haematopoietic Malignancies-A Review.

Authors:  Aleksandra Filipiuk; Agata Kozakiewicz; Kamil Kośmider; Monika Lejman; Joanna Zawitkowska
Journal:  Cancers (Basel)       Date:  2022-07-22       Impact factor: 6.575

2.  Exome sequencing identifies PD-L2 as a potential predisposition gene for lymphoma.

Authors:  Jianming Shao; Lei Gao; Marco L Leung; Bailey Gallinger; Cara Inglese; M Stephen Meyn; Daniela Del Gaudio; Soma Das; Zejuan Li
Journal:  Hematol Oncol       Date:  2022-05-29       Impact factor: 4.850

  2 in total

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