Evidence map›Paper›PMID 20440596›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2010

Depression of MAD2 inhibits apoptosis and increases proliferation and multidrug resistance in gastric cancer cells by regulating the activation of phosphorylated survivin.

Li Wang, Fang Yin, Yulei Du, Bei Chen, Shuhui Liang, Yongguo Zhang, Wenqi Du, Kaichun Wu, Jie Ding, Daiming Fan

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. A New Method for Chromosomes Preparation by ATP-Competitive Inhibitor SP600125Frontiers in bioengineering and biotechnology · 2020
    Article
  2. MAD2 Combined with Mitotic Spindle Apparatus (MSA) and Anticentromere Antibody (ACA) for Diagnosis of Small Cell Lung Cancer (SCLC).Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Disruption of FAT10-MAD2 binding inhibits tumor progression.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Genetic aspects of gastric cancer instability.TheScientificWorldJournal · 2012
    Review
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

10 authors at 2 institutions in 1 country.

Li WangState Key Laboratory of Cancer Biology & Digestive Diseases, of Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Fang Yin
Yulei Du
Bei Chen
Shuhui Liang
Yongguo Zhang
Wenqi Du
Kaichun Wu
Jie Ding
Daiming Fan
Air Force Medical University · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitotic arrest-deficient 2 (MAD2) is one of the essential mitotic spindle checkpoint regulators, and it can protect cells from aberrant chromosome segregation. The Mad2 gene is very rarely mutated in many kinds of human cancer, but aberrantly reduced expression of MAD2 has been correlated with defective mitotic checkpoints in several human cancers. We have previously found that the MAD2 expression level is also shown to be associated with the multidrug resistance of tumour cells. In this study, we constructed a small interfering RNA (siRNA) eukaryotic expression vector of MAD2 and downregulated MAD2 expression in the gastric cancer cell line SGC7901 by transfection of MAD2-siRNA. SGC7901 cells stably transfected with the MAD2-siRNA exhibited significantly increased expression of phosphorylated survivin protein and enhanced drug resistance. Furthermore, MAD2-siRNA suppressed the proliferation of SGC7901 cells and inhibited tumour formation in athymic nude mice. This study clearly reveals that downregulation of MAD2 could regulate the cell cycle, increase proliferation, and improve the drug resistance of gastric cancer cells by regulating the activation of phosphorylated survivin. It also suggests both that MAD2 might play an important role in the development of human gastric cancer and that silencing the MAD2 gene may help to deal with the multidrug resistance of gastric cancer cells.

Indexed as

ApoptosisCell ProliferationDrug Resistance, NeoplasmAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1Calcium-Binding ProteinsCell Cycle ProteinsCell Line, TumorCisplatinDown-RegulationDoxorubicinDrug Resistance, MultipleGene Expression Regulation, NeoplasticHumansInhibitor of Apoptosis ProteinsMad2 ProteinsAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1BIRC5 protein, humanCalcium-Binding ProteinsCell Cycle ProteinsCisplatinDoxorubicinInhibitor of Apoptosis ProteinsMAD2L1 protein, humanMad2 ProteinsMicrotubule-Associated ProteinsProto-Oncogene Proteins c-rafRepressor ProteinsRNA, Small InterferingSurvivin

Identifiers

PMID20440596
OpenAlexW2166698742

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.