A causal mechanism for childhood acute lymphoblastic leukaemia

M Greaves - Nature Reviews Cancer, 2018 - nature.com
In this Review, I present evidence supporting a multifactorial causation of childhood acute
lymphoblastic leukaemia (ALL), a major subtype of paediatric cancer. ALL evolves in two …

The prenatal origins of cancer

GM Marshall, DR Carter, BB Cheung, T Liu… - Nature Reviews …, 2014 - nature.com
The concept that some childhood malignancies arise from postnatally persistent embryonal
cells has a long history. Recent research has strengthened the links between driver …

In vivo functional screening for systems-level integrative cancer genomics

J Weber, CJ Braun, D Saur, R Rad - Nature reviews Cancer, 2020 - nature.com
With the genetic portraits of all major human malignancies now available, we next face the
challenge of characterizing the function of mutated genes, their downstream targets …

[HTML][HTML] A new human embryonic cell type associated with activity of young transposable elements allows definition of the inner cell mass

M Singh, AM Kondrashkina, TJ Widmann… - PLoS …, 2023 - journals.plos.org
There remains much that we do not understand about the earliest stages of human
development. On a gross level, there is evidence for apoptosis, but the nature of the affected …

Molecular processes involved in B cell acute lymphoblastic leukaemia

C Malouf, K Ottersbach - Cellular and molecular life sciences, 2018 - Springer
B cell leukaemia is one of the most frequent malignancies in the paediatric population, but
also affects a significant proportion of adults in developed countries. The majority of infant …

[HTML][HTML] Pathogenesis of ETV6/RUNX1-positive childhood acute lymphoblastic leukemia and mechanisms underlying its relapse

C Sun, L Chang, X Zhu - Oncotarget, 2017 - ncbi.nlm.nih.gov
Abstract ETV6/RUNX1 (E/R) is the most common fusion gene in childhood acute
lymphoblastic leukemia (ALL). Multiple lines of evidence imply a “two-hit” model for the …

A human IPS model implicates embryonic B-myeloid fate restriction as developmental susceptibility to B acute lymphoblastic leukemia-associated ETV6-RUNX1

C Böiers, SE Richardson, E Laycock, A Zriwil… - Developmental cell, 2018 - cell.com
ETV6-RUNX1 is associated with childhood acute B-lymphoblastic leukemia (cALL)
functioning as a first-hit mutation that initiates a clinically silent pre-leukemia in utero …

Cancer gene discovery: exploiting insertional mutagenesis

M Ranzani, S Annunziato, DJ Adams, E Montini - Molecular cancer research, 2013 - AACR
Insertional mutagenesis has been used as a functional forward genetics screen for the
identification of novel genes involved in the pathogenesis of human cancers. Different …

Commonly assessed markers in childhood BCP-ALL diagnostic panels and their association with genetic aberrations and outcome prediction

J Kulis, Ł Sędek, Ł Słota, B Perkowski, T Szczepański - Genes, 2022 - mdpi.com
Immunophenotypic characterization of leukemic cells with the use of flow cytometry (FC) is a
fundamental tool in acute lymphoblastic leukemia (ALL) diagnostics. A variety of genetic …

ETV6 Deficiency Unlocks ERG-Dependent Microsatellite Enhancers to Drive Aberrant Gene Activation in B-Lymphoblastic Leukemia

R Kodgule, JW Goldman, AC Monovich, T Saari… - Blood Cancer …, 2023 - AACR
Distal enhancers play critical roles in sustaining oncogenic gene-expression programs. We
identify aberrant enhancer-like activation of GGAA tandem repeats as a characteristic …