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FOXK2 gene expression in cancer:Potential regulatory mechanisms and clinical implicationsFOXK2 gene expression in cancer:Potential regulatory mechanisms and clinical implications

Renata Ivo Vasconcelos Luciana da Torre Carneiro Raquel Ciuvalschi Maia Thaıis Hancio Gabriela Nestal de Moraes

Genes & Diseases2026，Vol.13Issue(4)：P.305-314,10.

Genes & Diseases2026，Vol.13Issue(4)：P.305-314,10.DOI:10.1016/j.gendis.2025.101951

FOXK2 gene expression in cancer:Potential regulatory mechanisms and clinical implicationsFOXK2 gene expression in cancer:Potential regulatory mechanisms and clinical implications

Renata Ivo Vasconcelos ¹Luciana da Torre Carneiro ¹Raquel Ciuvalschi Maia ²Thaıis Hancio ³Gabriela Nestal de Moraes¹

作者信息

1. Instituto de Bioquimica Medica Leopoldo de Meis,Universidade Federal do Rio de Janeiro(UFRJ),Avenida Carlos Chagas Filho,373,2°andar,H2-003,Cidade Universitaria,Rio de Janeiro 21941599,Brazil
2. Programa de Hemato-Oncologia Molecular,Instituto Nacional do Cancer(INCA),Praca da CruzVermelha,23,6°andar,Centro,Rio de Janeiro 20230130,Brazil
3. Laboratorio Nacional de Biociencias(LNBio),Centro Nacional de Pesquisa em Energia e Materiais(CNPEM),Polo II de Alta Tecnologia,R.Giuseppe Maximo Scolfaro,10000,Bosque das Palmeiras,Campinas,Sao Paulo 13083100,Brazil
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摘要

关键词

Cancer/Clinical outcomes/FOXK2 transcriptionfactor/Gene alterations/Transcript expression

分类

医药卫生

引用本文复制引用

Renata Ivo Vasconcelos,Luciana da Torre Carneiro,Raquel Ciuvalschi Maia,Thaıis Hancio,Gabriela Nestal de Moraes..FOXK2 gene expression in cancer:Potential regulatory mechanisms and clinical implicationsFOXK2 gene expression in cancer:Potential regulatory mechanisms and clinical implications[J].Genes & Diseases,2026,13(4):P.305-314,10.

基金项目

supported by grants from L''oreal-UNESCO-ABC For Women in Science （）

Carlos Chagas Filho Foundation for Research Support of the State of Rio de Janeiro(FAPERJ No.SEI-26003/004812/2021 and SEl-260003/001554/2022) （FAPERJ No.SEI-26003/004812/2021 and SEl-260003/001554/2022）

the National Council for Scientific and Technological Development(CNPq No.307427/2022-6 and 408314/2021-4) （CNPq No.307427/2022-6 and 408314/2021-4）

R.I.V and L.T.C were supported by CNPq fellowships.R.C.M is supported by FAPERJ(No.260003/007036/2022) （No.260003/007036/2022）

Our laboratory was also supported by grants from the CNPq-INCT program(No.408340/2024-0) （No.408340/2024-0）

The funding agencies have not been involved in the study design,data collection,analysis and interpretation or writing of the manuscript. （）

Genes & Diseases

ISSN：2352-4820

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