Results 31 to 40 of about 7,235 (159)

KDM6A addiction of cervical carcinoma cell lines is triggered by E7 and mediated by p21CIP1 suppression of replication stress. [PDF]

open access: yesPLoS Pathogens, 2017
Expression of E7 proteins encoded by carcinogenic, high-risk human papillomaviruses (HPVs) triggers increased expression of the histone H3 lysine 27 demethylase KDM6A.
David R Soto   +3 more
doaj   +1 more source

Histone demethylase KDM6A coordinating with KMT2B regulates self-renewal and chemoresistance of non-small cell lung cancer stem cells

open access: yesTranslational Oncology, 2023
Background and aims: Wnt signaling is essential for the maintenance of cancer stem cells (CSCs), but mutations in the β-catenin and APC genes are less common in non-small cell lung carcinoma (NSCLC).
Zhiwei Chen   +3 more
doaj   +1 more source

The Role of Kdm6a in Normal Hematopoiesis

open access: yesBlood, 2016
Abstract The role of the X-linked H3K27 demethylase KDM6A in normal hematopoiesis remains unclear. We generated Kdm6a conditional knockout mice (with LoxP sites flanking the 3rd exon) and crossed these mice with Vav1-Cre mice to inactivate Kdm6a in hematopoietic stem/progenitor cells.
Ling Tian, Lukas D. Wartman
openaire   +2 more sources

Gender disparities in clinical outcomes of urothelial carcinoma linked to X chromosome gene KDM6A mutation

open access: yesBMJ Oncology, 2023
Objective KDM6A, a representative tumour suppressor gene with sex bias, is frequently altered in urothelial carcinoma (UC). The specific impacts of KDM6A mutations on gender-based clinical outcomes in UC remain poorly understood.Methods and analysis We ...
Weijuan Zhang   +14 more
doaj   +1 more source

Metformin directly targets the H3K27me3 demethylase KDM6A/UTX [PDF]

open access: yesAging Cell, 2018
SummaryMetformin, the first drug chosen to be tested in a clinical trial aimed to target the biology of aging per se, has been clinically exploited for decades in the absence of a complete understanding of its therapeutic targets or chemical determinants.
Elisabet Cuyàs   +14 more
openaire   +5 more sources

SMARCA4 deficient tumours are vulnerable to KDM6A/UTX and KDM6B/JMJD3 blockade [PDF]

open access: yesNature Communications, 2021
Abstract Despite the genetic inactivation of SMARCA4 , a core component of the SWI/SNF-complex commonly found in cancer, there are no therapies that effectively target SMARCA4-deficient tumours. Here, we show that, unlike the cells with activated MYC
Octavio A. Romero   +19 more
openaire   +9 more sources

The histone demethylase UTX/KDM6A in cancer: Progress and puzzles [PDF]

open access: yesInternational Journal of Cancer, 2019
The lysine‐specific demethylase 6A/UTX (gene name KDM6A) acts as a component of the COMPASS complex to control gene activation. UTX demethylates H3K27me2/3 at genes and enhancers. Deleterious mutations in KDM6A are found in many cancer types, prominently urothelial carcinoma and certain T‐cell leukemias.
Wolfgang A. Schulz   +3 more
openaire   +2 more sources

KDM6A facilitates Xist upregulation at the onset of X inactivation

open access: yes, 2023
Abstract X chromosome inactivation (XCI) is a female-specific process in which one X chromosome is silenced to balance X-linked gene expression between the sexes. XCI is initiated in early development by upregulation of the lncRNA Xist on the future inactive X (Xi).
Josephine Lin   +10 more
openaire   +2 more sources

KDM6A mutations promote acute cytoplasmic DNA release, DNA damage response and mitosis defects

open access: yesBMC Molecular and Cell Biology, 2021
Background KDM6A, encoding a histone demethylase, is one of the top ten mutated epigenetic cancer genes. The effect of mutations on its structure and function are however poorly characterized.
J. Koch   +5 more
doaj   +1 more source

H3K27me3 Demethylases Maintain the Transcriptional and Epigenomic Landscape of the Intestinal EpitheliumSummary

open access: yesCellular and Molecular Gastroenterology and Hepatology, 2023
Background & Aims: Although trimethylation of histone H3 lysine 27 (H3K27me3) by polycomb repressive complex 2 is required for intestinal function, the role of the antagonistic process—H3K27me3 demethylation—in the intestine remains unknown.
Hannah M. Kolev   +6 more
doaj   +1 more source

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