Not only a therapeutic target; mTOR in Hodgkin lymphoma and acute lymphoblastic leukemia

被引:2
|
作者
Mendoza, Miguel Enrique Cuellar [1 ,2 ]
Sanchez, Francisco Raul Chavez [1 ]
Acosta, Elisa Maria Dorantes [3 ]
Zuniga, Ana Maria Niembro [4 ]
Pelayo, Rosana [5 ]
Tarres, Marta Zapata [2 ]
机构
[1] Univ Nacl Autonoma Mexico, Med Fac, Dept Biochem, Mexico City, Mexico
[2] IMSS Fdn, Res Coordinat, Mexico City, Mexico
[3] Mexican Childrens Hosp Federico Gomez, Leukemia Clin, Mexico City, Mexico
[4] Nacl Inst Pediat, Oncol Dept, Mexico City, Mexico
[5] Mexican Inst Social Secur, Educ & Res Unit, Mexico City, Mexico
来源
FRONTIERS IN ONCOLOGY | 2024年 / 14卷
关键词
mTOR; acute lymphoblastic leukemia; Hodgkin lymphoma; mTORC1; mTORC2; SIGNALING PATHWAYS; PROLIFERATION; CELLS; DIFFERENTIATION; EVEROLIMUS; SURVIVAL; KINASE; NOTCH1;
D O I
10.3389/fonc.2024.1304605
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
<bold>Introduction:</bold> The mechanistic/mammalian target of rapamycin (mTOR) is a serine/threonine kinase, which is downregulated or upregulated and is implicated in different types of cancer including hematologic neoplasms, skin prostate, and head and neck cancer. <bold>Aim:</bold> The aim of this study was to explore the current knowledge of mTOR signaling in acute lymphoblastic leukemia and Hodgkin lymphoma. <bold>Methods:</bold> A systematic review was performed according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, searching PubMed, Discovery Service for National Autonomous University of Mexico, Registro Nacional de Instituciones y Empresas Cient & iacute;ficas y Tecnol & oacute;gicas (RENIECYT), and Scientific Electronic Library Online (SciELO) from 1994 to 2023. A total of 269 papers were identified for acute lymphoblastic leukemia, but based on specific criteria, 15 were included; for Hodgkin lymphoma, 110 papers were identified, but 5 were included after manual searching. <bold>Results:</bold> A total of 20 papers were evaluated, where mTOR activity is increased in patients with Hodgkin lymphoma and acute lymphoblastic leukemia by different molecular mechanisms. <bold>Conclusions:</bold> mTOR activity is increased in patients with both hematologic neoplasms and NOTCH; interleukin 4, 7, and 9, and nuclear proteins have been studied for their role in the activation of mTOR signaling.
引用
收藏
页数:6
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