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Low BCL7A expression predicts poor prognosis in ovarian cancer.
Sun Z, Sun L, He M, Pang Y, Yang Z, Wang J. Sun Z, et al. J Ovarian Res. 2019 May 10;12(1):41. doi: 10.1186/s13048-019-0518-0. J Ovarian Res. 2019. PMID: 31077237 Free PMC article.
We aimed to study the prognostic role of BCL7A in ovarian cancer. RESULTS: Through data mining of RNAseq data from the Cancer Genome Atlas database (TCGA), we explored the clinical relevance of BCL7A mRNA expression. ...CONCLUSIONS: Low BCL7A ex …
We aimed to study the prognostic role of BCL7A in ovarian cancer. RESULTS: Through data mining of RNAseq data from the Canc
BCL7A inhibits the progression and drug-resistance in acute myeloid leukemia.
Li T, Gao R, Xu K, Pan P, Chen C, Wang D, Zhang K, Qiao J, Gu Y. Li T, et al. Drug Resist Updat. 2024 Sep;76:101120. doi: 10.1016/j.drup.2024.101120. Epub 2024 Jul 22. Drug Resist Updat. 2024. PMID: 39053383 Free article.
AIMS: This study aimed to elucidate the biological roles and regulatory mechanisms of B-cell lymphoma 7 protein family member A (BCL7A) in acute myeloid leukemia (AML), particularly its interaction with polypyrimidine tract binding protein 1 (PTBP1) and the effects on c
AIMS: This study aimed to elucidate the biological roles and regulatory mechanisms of B-cell lymphoma 7 protein family member A (BCL7A
BCL7A is silenced by hypermethylation to promote acute myeloid leukemia.
Patiño-Mercau JR, Baliñas-Gavira C, Andrades A, Benitez-Cantos MS, Rot AE, Rodriguez MI, Álvarez-Pérez JC, Cuadros M, Medina PP. Patiño-Mercau JR, et al. Biomark Res. 2023 Mar 20;11(1):32. doi: 10.1186/s40364-023-00472-x. Biomark Res. 2023. PMID: 36941700 Free PMC article.
Cell competition assays after BCL7A expression restoration were used to assess the role of BCL7A in AML cell line models. ...The AML-derived cell line NB4 silenced the BCL7A expression via promoter hypermethylation. Ectopic BCL7A expression in AML cell …
Cell competition assays after BCL7A expression restoration were used to assess the role of BCL7A in AML cell line models. ...T …
SWI/SNF complexes in hematological malignancies: biological implications and therapeutic opportunities.
Andrades A, Peinado P, Alvarez-Perez JC, Sanjuan-Hidalgo J, García DJ, Arenas AM, Matia-González AM, Medina PP. Andrades A, et al. Mol Cancer. 2023 Feb 21;22(1):39. doi: 10.1186/s12943-023-01736-8. Mol Cancer. 2023. PMID: 36810086 Free PMC article. Review.
Furthermore, alterations in SWI/SNF complex subunits, especially in ARID1A/1B/2, SMARCA2/4, and BCL7A, are highly recurrent across a wide variety of lymphoid and myeloid malignancies. ...These alterations, as well as their synthetic lethal relationships with SWI/SNF and no …
Furthermore, alterations in SWI/SNF complex subunits, especially in ARID1A/1B/2, SMARCA2/4, and BCL7A, are highly recurrent across a …
Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy.
Kadoch C, Hargreaves DC, Hodges C, Elias L, Ho L, Ranish J, Crabtree GR. Kadoch C, et al. Nat Genet. 2013 Jun;45(6):592-601. doi: 10.1038/ng.2628. Epub 2013 May 5. Nat Genet. 2013. PMID: 23644491 Free PMC article.
Our analysis suggests that specific subunits protect against cancer in specific tissues. In addition, mutations affecting more than one subunit, defined here as compound heterozygosity, are prevalent in certain cancers. Our studies demonstrate that mSWI/SNF is the m …
Our analysis suggests that specific subunits protect against cancer in specific tissues. In addition, mutations affecting more than o …
Using bioinformatics approaches to investigate driver genes and identify BCL7A as a prognostic gene in colorectal cancer.
Chao JY, Chang HC, Jiang JK, Yang CY, Chen FH, Lai YL, Lin WJ, Li CY, Wang SC, Yang MH, Lin YF, Cheng WC. Chao JY, et al. Comput Struct Biotechnol J. 2021 Jul 1;19:3922-3929. doi: 10.1016/j.csbj.2021.06.044. eCollection 2021. Comput Struct Biotechnol J. 2021. PMID: 34306573 Free PMC article.
Colorectal cancer (CRC) results from the uncontrolled growth of cells in the colon, rectum, or appendix. ...These findings may be of value in clinical early cancer detection, disease monitoring, drug development, and treatment efforts in the future....
Colorectal cancer (CRC) results from the uncontrolled growth of cells in the colon, rectum, or appendix. ...These findings may be of …
A Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve.
Siguero-Álvarez M, Salguero-Jiménez A, Grego-Bessa J, de la Barrera J, MacGrogan D, Prados B, Sánchez-Sáez F, Piñeiro-Sabarís R, Felipe-Medina N, Torroja C, Gómez MJ, Sabater-Molina M, Escribá R, Richaud-Patin I, Iglesias-García O, Sbroggio M, Callejas S, O'Regan DP, McGurk KA, Dopazo A, Giovinazzo G, Ibañez B, Monserrat L, Pérez-Pomares JM, Sánchez-Cabo F, Pendas AM, Raya A, Gimeno-Blanes JR, de la Pompa JL. Siguero-Álvarez M, et al. Circulation. 2023 Jan 3;147(1):47-65. doi: 10.1161/CIRCULATIONAHA.121.058767. Epub 2022 Nov 3. Circulation. 2023. PMID: 36325906 Free article.
Whole exome sequencing of LVNC families revealed single-nucleotide gene variants of ASXL3, APCDD1, TMX3, CEP192, and BCL7A cosegregating with the MIB1 mutations and LVNC. In experiments with mice harboring the orthologous variants on the corresponding Mib1 backgrounds, tri …
Whole exome sequencing of LVNC families revealed single-nucleotide gene variants of ASXL3, APCDD1, TMX3, CEP192, and BCL7A cosegregat …
The whole-genome landscape of Burkitt lymphoma subtypes.
Panea RI, Love CL, Shingleton JR, Reddy A, Bailey JA, Moormann AM, Otieno JA, Ong'echa JM, Oduor CI, Schroeder KMS, Masalu N, Chao NJ, Agajanian M, Major MB, Fedoriw Y, Richards KL, Rymkiewicz G, Miles RR, Alobeid B, Bhagat G, Flowers CR, Ondrejka SL, Hsi ED, Choi WWL, Au-Yeung RKH, Hartmann W, Lenz G, Meyerson H, Lin YY, Zhuang Y, Luftig MA, Waldrop A, Dave T, Thakkar D, Sahay H, Li G, Palus BC, Seshadri V, Kim SY, Gascoyne RD, Levy S, Mukhopadyay M, Dunson DB, Dave SS. Panea RI, et al. Blood. 2019 Nov 7;134(19):1598-1607. doi: 10.1182/blood.2019001880. Blood. 2019. PMID: 31558468 Free PMC article.
Although sporadic and immunodeficiency-associated BLs had similar genetic profiles, endemic BLs manifested more frequent mutations in BCL7A and BCL6 and fewer genetic alterations in DNMT1, SNTB2, and CTCF. Silencing mutations in ID3 were a common feature of all 3 subtypes …
Although sporadic and immunodeficiency-associated BLs had similar genetic profiles, endemic BLs manifested more frequent mutations in BCL
Structure of the nucleosome-bound human BCL7A.
Martin F, Kazrani AA, Lafouge J, Diaz-Jimenez DM, Siebert S, Fabbro-Burtschell L, Maillard E, Lapouge K, Mertens HDT, Sauter C, Leitner A, Ochsenbein F, Blais A, Bergamin E. Martin F, et al. Nucleic Acids Res. 2025 Apr 10;53(7):gkaf273. doi: 10.1093/nar/gkaf273. Nucleic Acids Res. 2025. PMID: 40207634 Free PMC article.
Their function in the complex is unknown, and very limited structural information is available, despite the fact that they are mutated in several cancer types, most notably blood malignancies and hence medically relevant. Here, using cryo-electron microscopy in combination …
Their function in the complex is unknown, and very limited structural information is available, despite the fact that they are mutated in se …
BCL7C suppresses ovarian cancer growth by inactivating mutant p53.
Huang C, Hao Q, Shi G, Zhou X, Zhang Y. Huang C, et al. J Mol Cell Biol. 2021 May 7;13(2):141-150. doi: 10.1093/jmcb/mjaa065. J Mol Cell Biol. 2021. PMID: 33306126 Free PMC article.
B-cell CLL/lymphoma 7 protein family member C (BCL7C) located at chromosome 16p11.2 shares partial sequence homology with the other two family members, BCL7A and BCL7B. Its role in cancer remains completely unknown. Here, we report our finding of its tumor-suppressi …
B-cell CLL/lymphoma 7 protein family member C (BCL7C) located at chromosome 16p11.2 shares partial sequence homology with the other two fami …
43 results