Evidence map›Paper›PMID 19755862›Full record

ArticleCell cycle (Georgetown, Tex.)2009

Involvement of MKP-1 and Bcl-2 in acquired cisplatin resistance in ovarian cancer cells.

Juan Wang, Jun-Ying Zhou, Lianfeng Zhang, Gen Sheng Wu

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Dual-specificity phosphatases: therapeutic targets in cancer therapy resistance.Journal of cancer research and clinical oncology · 2022
    Review
  6. A worldwide bibliometric analysis of triptolide research from 1997 to 2021.American journal of translational research · 2022
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 4 countries.

Juan WangProgram in Molecular Biology and Genetics, Karmanos Cancer Institute, Department of Pathology, Wayne State University School of Medicine, Detroit, MI, USA.
Jun-Ying Zhou
Lianfeng Zhang
Gen Sheng Wu
Chinese Academy of Medical Sciences & Peking Union Medical College · CNSchlumberger (Ireland) · IEWayne State University · US

Funding

The Role of Phosphatase CL100/MKP1 in Human CancerR01CA100073 · NCI · WAYNE STATE UNIVERSITY · PI WU, GEN SHENG · 2004 to 2009
$1.3M
NCI NIH HHS R01 CA100073
6 · The paper itself

Abstract

Although cisplatin is a very effective anticancer agent against several types of cancer including ovarian cancer, the mechanisms of acquired resistance are not fully understood. By chronically exposing cisplatin to ovarian cancer cell lines, we established two cisplatin-resistant cell lines OV433 and TOV112D. Our results indicate that the mechanisms underlying their cisplatin resistance are distinct. In OV433 cells, cisplatin resistance is associated with increased expression of mitogen-activated protein kinase (MAPK) phosphatase-1 (MKP-1). By knocking down MKP-1 expression by siRNA or inhibiting MKP-1 expression by its pharmacological inhibitor triptolide, cisplatin-resistant OV433 cells became cisplatin-sensitive and subsequently increased cisplatin-induced apoptosis. In TOV112D cells, on the other hand, acquired cisplatin resistance is associated with increased levels of Bcl-2 protein. By inhibiting the activity of Bcl-2 protein with its pharmacological inhibitor gossypol or knocking down Bcl-2 expression by siRNA, cisplatin-resistant TOV112D cells became cisplatin-sensitive and subsequently increased cisplatin-induced apoptosis. Therefore, our data suggest that the mechanisms of acquired cisplatin resistance vary among ovarian cancer cells, which involve upregulation of molecules associated with the cell survival pathways.

Indexed as

Antineoplastic AgentsApoptosisCisplatinDrug Resistance, NeoplasmDual Specificity Phosphatase 1FemaleGene Knockdown TechniquesHumansOvarian NeoplasmsProto-Oncogene Proteins c-bcl-2RNA, Small InterferingAntineoplastic AgentsCisplatinDual Specificity Phosphatase 1DUSP1 protein, humanProto-Oncogene Proteins c-bcl-2RNA, Small Interfering

Identifiers

PMID19755862
PMCPMC4063298
OpenAlexW2021529896

What OpenQuestion holds

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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.