Fanconi anemia proteins and genome fragility: unraveling replication defects for cancer therapy

NB Fajardo, S Taraviras, Z Lygerou - Trends in Cancer, 2022 - cell.com
Accurate and complete genome duplication is crucial to maintain cell survival and prevent
malignant transformation. The Fanconi anemia (FA) pathway has traditionally been …

NHEJ-mediated repair of CRISPR-Cas9-induced DNA breaks efficiently corrects mutations in HSPCs from patients with fanconi anemia

FJ Román-Rodríguez, L Ugalde, L Álvarez, B Díez… - Cell Stem Cell, 2019 - cell.com
Non-homologous end-joining (NHEJ) is the preferred mechanism used by hematopoietic
stem cells (HSCs) to repair double-stranded DNA breaks and is particularly increased in …

Gene expression and mutation-guided synthetic lethality eradicates proliferating and quiescent leukemia cells

M Nieborowska-Skorska, K Sullivan… - The Journal of …, 2017 - Am Soc Clin Investig
Quiescent and proliferating leukemia cells accumulate highly lethal DNA double-strand
breaks that are repaired by 2 major mechanisms: BRCA-dependent homologous …

LepR+ niche cell–derived AREG compromises hematopoietic stem cell maintenance under conditions of DNA repair deficiency and aging

L Wu, Q Lin, S Chatla, S Amarachintha, AF Wilson… - Blood, 2023 - ashpublications.org
The cross talk between extrinsic niche-derived and intrinsic hematopoietic stem cell (HSC)
factors controlling HSC maintenance remains elusive. Here, we demonstrated that …

High-throughput screening platform for nanoparticle-mediated alterations of DNA repair capacity

SM Toprani, D Bitounis, Q Huang, N Oliveira, KW Ng… - ACS …, 2021 - ACS Publications
The potential genotoxic effects of engineered nanomaterials (ENMs) may occur through the
induction of DNA damage or the disruption of DNA repair processes. Inefficient DNA repair …

Baboon Envelope Pseudotyped “Nanoblades” Carrying Cas9/gRNA Complexes Allow Efficient Genome Editing in Human T, B, and CD34+ Cells and Knock-in of AAV6 …

A Gutierrez-Guerrero, MJ Abrey Recalde… - Frontiers in Genome …, 2021 - frontiersin.org
Programmable nucleases have enabled rapid and accessible genome engineering in
eukaryotic cells and living organisms. However, their delivery into human blood cells can be …

Hes1 deficiency causes hematopoietic stem cell exhaustion

Z Ma, J Xu, L Wu, J Wang, Q Lin, FA Chowdhury… - Stem Cells, 2020 - academic.oup.com
Abstract The transcriptional repressor Hairy Enhancer of Split 1 (HES1) plays an essential
role in the development of many organs by promoting the maintenance of stem/progenitor …

The ubiquitin family meets the Fanconi anemia proteins

X Renaudin, LK Lerner, CFM Menck… - … Research/Reviews in …, 2016 - Elsevier
Fanconi anaemia (FA) is a hereditary disorder characterized by bone marrow failure,
developmental defects, predisposition to cancer and chromosomal abnormalities. FA is …

A germline FANCA alteration that is associated with increased sensitivity to DNA damaging agents

DC Wilkes, V Sailer, H Xue… - Molecular …, 2017 - molecularcasestudies.cshlp.org
Defects in genes involved in DNA damage repair (DDR) pathway are emerging as novel
biomarkers and targets for new prostate cancer drug therapies. A previous report revealed …

Rare variants in Fanconi anemia genes are enriched in acute myeloid leukemia

KZY Maung, PJ Leo, M Bassal, DA Casolari… - Blood Cancer …, 2018 - nature.com
Acute Myeloid Leukemia (AML) is an aggressive hematological malignancy caused by
somatically acquired changes affecting a well-defined set of genes 1. While rare high-risk …