Evidence map›Paper›PMID 25915840›Full record

ArticleOncogene2016

HUS1 regulates in vivo responses to genotoxic chemotherapies.

G Balmus, P X Lim, A Oswald, K R Hume, A Cassano, J Pierre, A Hill, W Huang, A August, T Stokol and 2 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

G BalmusDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
P X LimDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
A OswaldDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
K R HumeDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
A CassanoDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
J PierreDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
A HillDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
W HuangDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
A AugustDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0003-4968-3415
T StokolDepartment of Population Medicine and Diagnostic Sciences, Cornell University, Ithaca, NY, USA.
T SouthardDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
R S WeissDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, USA.
Cornell University · US

Funding

Genome maintenance by the mouse Hus1 checkpoint geneR01CA108773 · NCI · CORNELL UNIVERSITY ITHACA · PI WEISS, ROBERT S · 2004 to 2013
$2.5M
Mark I Model 68 Gamma IrradiatorS10RR023781 · NCRR · CORNELL UNIVERSITY · PI WEISS, ROBERT S · 2007 to 2007
$234k
NCI NIH HHS R01 CA108773NCRR NIH HHS S10RR023781
6 · The paper itself

Abstract

Cells are under constant attack from genotoxins and rely on a multifaceted DNA damage response (DDR) network to maintain genomic integrity. Central to the DDR are the ATM and ATR kinases, which respond primarily to double-strand DNA breaks (DSBs) and replication stress, respectively. Optimal ATR signaling requires the RAD9A-RAD1-HUS1 (9-1-1) complex, a toroidal clamp that is loaded at damage sites and scaffolds signaling and repair factors. Whereas complete ATR pathway inactivation causes embryonic lethality, partial Hus1 impairment has been accomplished in adult mice using hypomorphic (Hus1(neo)) and null (Hus1(Δ1)) Hus1 alleles, and here we use this system to define the tissue- and cell type-specific actions of the HUS1-mediated DDR in vivo. Hus1(neo/Δ1) mice showed hypersensitivity to agents that cause replication stress, including the crosslinking agent mitomycin C (MMC) and the replication inhibitor hydroxyurea, but not the DSB inducer ionizing radiation. Analysis of tissue morphology, genomic instability, cell proliferation and apoptosis revealed that MMC treatment caused severe damage in highly replicating tissues of mice with partial Hus1 inactivation. The role of the 9-1-1 complex in responding to MMC was partially ATR-independent, as a HUS1 mutant that was proficient for ATR-induced checkpoint kinase 1 phosphorylation nevertheless conferred MMC hypersensitivity. To assess the interplay between the ATM and ATR pathways in responding to replication stress in vivo, we used Hus1/Atm double mutant mice. Whereas Hus1(neo/neo) and Atm(-/-) single mutant mice survived low-dose MMC similar to wild-type controls, Hus1(neo/neo)Atm(-/-) double mutants showed striking MMC hypersensitivity, consistent with a model in which MMC exposure in the context of Hus1 dysfunction results in DSBs to which the ATM pathway normally responds. This improved understanding of the inter-dependency between two major DDR mechanisms during the response to a conventional chemotherapeutic illustrates how inhibition of checkpoint factors such as HUS1 may be effective for the treatment of ATM-deficient and other cancers.

Indexed as

AnimalsAtaxia Telangiectasia Mutated ProteinsCell Cycle ProteinsDNA DamageMiceMutagenicity TestsMutagensSignal TransductionAtaxia Telangiectasia Mutated ProteinsAtm protein, mouseATR protein, humanCell Cycle ProteinsHus1 protein, mouseMutagens

Identifiers

PMID25915840
OpenAlexW1987303163

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.