Evidence map›Paper›PMID 22439007›Full record

ArticlePloS one2012

Inhibition of ERβ induces resistance to cisplatin by enhancing Rad51-mediated DNA repair in human medulloblastoma cell lines.

Anna Wilk, Agnieszka Waligorska, Piotr Waligorski, Augusto Ochoa, Krzysztof Reiss

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Linking DNA Damage and Hormone Signaling Pathways in Cancer.Trends in endocrinology and metabolism: TEM · 2016
    Review
  12. ATM may be a protective factor in endometrial carcinogenesis with the progesterone pathway.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  13. Article
  14. Article
  15. 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

5 authors at 1 institution in 1 country.

Anna WilkNeurological Cancer Research, Department of Medicine, LSU Health Sciences Center, New Orleans, Louisiana, United States of America.
Agnieszka Waligorska
Piotr Waligorski
Augusto Ochoa
Krzysztof Reiss
Louisiana State University Health Sciences Center New Orleans · US

Funding

Arginase Production in Cancer: Evading Immune ResponseR01CA107974 · NCI · LSU HEALTH SCIENCES CENTER · PI OCHOA, AUGUSTO C. · 2004 to 2015
$3.6M
Nuclear IRS-1-DNA repair and mutagenesis in medulloblastomaR01CA095518 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI REISS, KRZYSZTOF · 2002 to 2012
$2.6M
NCI NIH HHS R01 CA095518NCI NIH HHS R01CA095518NCI NIH HHS R01 CA107974
6 · The paper itself

Abstract

Cisplatin is one of the most widely used and effective anticancer drugs against solid tumors including cerebellar tumor of the childhood, Medulloblastoma. However, cancer cells often develop resistance to cisplatin, which limits therapeutic effectiveness of this otherwise effective genotoxic drug. In this study, we demonstrate that human medulloblastoma cell lines develop acute resistance to cisplatin in the presence of estrogen receptor (ER) antagonist, ICI182,780. This unexpected finding involves a switch from the G2/M to G1 checkpoint accompanied by decrease in ATM/Chk2 and increase in ATR/Chk1 phosphorylation. We have previously reported that ERβ, which is highly expressed in medulloblastomas, translocates insulin receptor substrate 1 (IRS-1) to the nucleus, and that nuclear IRS-1 binds to Rad51 and attenuates homologous recombination directed DNA repair (HRR). Here, we demonstrate that in the presence of ICI182,780, cisplatin-treated medulloblastoma cells show recruitment of Rad51 to the sites of damaged DNA and increase in HRR activity. This enhanced DNA repair during the S phase preserved also clonogenic potential of medulloblastoma cells treated with cisplatin. In conclusion, inhibition of ERβ considered as a supplemental anticancer therapy, has been found to interfere with cisplatin-induced cytotoxicity in human medulloblastoma cell lines.

Indexed as

Antineoplastic AgentsBase SequenceCell Line, TumorCell SurvivalCisplatinDNA DamageDNA RepairDrug InteractionsDrug Resistance, NeoplasmEstradiolEstrogen AntagonistsEstrogen Receptor betaFulvestrantHumansMedulloblastomaRad51 RecombinaseAntineoplastic AgentsCisplatinEstradiolEstrogen AntagonistsEstrogen Receptor betaFulvestrantRAD51 protein, humanRad51 RecombinaseRNA, Small Interfering

Identifiers

PMID22439007
PMCPMC3306313
OpenAlexW1981795687

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.