Evidence map›Paper›PMID 24283650›Full record

ArticleJournal of hematology & oncology2013

Differential responses to genotoxic agents between induced pluripotent stem cells and tumor cell lines.

Yinghua Lu, Dazhong Xu, Jing Zhou, Yupo Ma, Yongping Jiang, Wenxian Zeng, Wei Dai

Open access · goldAbstract read
In one paragraph

Article in Journal of hematology & oncology, 2013. 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
0.9field-weighted citation impact, top 25% 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, 14 citations in OpenAlex.

  1. Exploring the effects of topoisomerase II inhibitor XK469 on anthracycline cardiotoxicity and DNA damage.Toxicological sciences : an official journal of the Society of Toxicology · 2024
    Article
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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

7 authors at 5 institutions in 2 countries.

Yinghua Lu
Dazhong Xu
Jing Zhou
Yupo Ma
Yongping Jiang
Wenxian ZengCollege of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, China. zengwnxian@hotmail.com.
Wei Dai
NYU Langone Health · USChinese Academy of Medical Sciences & Peking Union Medical College · CNNew York University · USNorth West Agriculture and Forestry University · CNState University of New York · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
RESEARCH IN ENVIRONMENTAL HEALTH SCIENCES (CENTER GRANT)P30ES000260 · NIEHS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI COSTA, MAX · 1985 to 2020
$26.1M
Molecular mechanisms underlying chromosomal instability and aneuploidyR01CA090658 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DAI, WEI · 2001 to 2012
$2.9M
Mechanisms of arsenic-induced chromosomal instability and carcinogenesisR01ES020591 · NIEHS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DAI, WEI · 2012 to 2016
$2.0M
Plk3, A New Player In The Hypoxia Regulatory Networ.R01CA150512 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DAI, WEI · 2011 to 2015
$1.6M
Plk3 in lung cancerR03ES019929 · NIEHS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI XU, DAZHONG · 2011 to 2012
$160k
NCI NIH HHS CA090658NCI NIH HHS P30 CA016087NCI NIH HHS R01 CA150512NIEHS NIH HHS ES000260NIEHS NIH HHS ES019929NIEHS NIH HHS R01 ES020591
6 · The paper itself

Abstract

Given potential values of induced pluripotent stem (iPS) cells in basic biomedical research and regenerative medicine, it is important to understand how these cells regulate their genome stability in response to environmental toxins and carcinogens. The present study characterized the effect of Cr(VI), a well-known genotoxic agent and environmental carcinogen, on major molecular components of DNA damage response pathways in human iPS cells. We compared the effect of Cr(VI) on human iPS cells with two established cell lines, Tera-1 (teratoma origin) and BEAS-2B (lung epithelial origin). We also studied the effect of hydrogen peroxide and doxorubicin on modulating DNA damage responses in these cell types. We demonstrated that ATM and p53 phosphorylation is differentially regulated in human iPS cells compared with Tera-1 and BEAS-2B cells after exposure to various genotoxic agents. Moreover, we observed that inhibition of CK2, but not p38, promotes phosphorylation of p53S392 in iPS cells. Combined, our data reveal some unique features of DNA damage responses in human iPS cells.

Indexed as

DNA DamageCell Line, TumorChromium CompoundsDose-Response Relationship, DrugDoxorubicinHumansHydrogen PeroxideInduced Pluripotent Stem CellsLung NeoplasmsMutagensPhosphorylationTeratomaTumor Suppressor Protein p53Chromium CompoundsDoxorubicinHydrogen PeroxideMutagensTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID24283650
PMCPMC3856456
OpenAlexW2123932894

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.