Evidence map›Paper›PMID 19775288›Full record

ArticleCancer science2010

SIAH1 induced apoptosis by activation of the JNK pathway and inhibited invasion by inactivation of the ERK pathway in breast cancer cells.

Yuan-Yuan Wen, Zhi-Qiang Yang, Min Song, Bai-Lin Li, Ji-Jiang Zhu, En-Hua Wang

Open access · greenAbstract read
In one paragraph

Article in Cancer science, 2010. 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
1.1field-weighted citation impact, top 26% 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, 35 citations in OpenAlex.

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  12. Regulators and effectors of Siah ubiquitin ligases.Cell biochemistry and biophysics · 2013
    Review
  13. An upregulation of SIAH1 after spinal cord injury in adult rats.Journal of molecular neuroscience : MN · 2011
    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

6 authors at 1 institution in 1 country.

Yuan-Yuan WenDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Sciences of China Medical University, Shenyang, China.
Zhi-Qiang Yang
Min Song
Bai-Lin Li
Ji-Jiang Zhu
En-Hua Wang
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Seven in absentia homolog 1 (SIAH1), a homologue of Drosophila seven in absentia (Sina), has emerged as a tumor suppressor and plays an important role in regulating cell apoptosis. To investigate the role and possible mechanism of SIAH1 in breast cancer cells, we up-regulated the expression of SIAH1 using pcDNA3-myc-SIAH1 and knocked down SIAH1 using SIAH1 siRNA. We found that the overexpression of SIAH1 induced cell apoptosis by up-regulating the level of Bim through the activation of the JNK signaling pathway, and the suppression of SIAH1 expression increased cell invasion via the activation of the ERK signaling pathway in breast cancer cells. All these results indicate that the JNK and ERK signaling pathways may play an important role in the SIAH1-dependent biological behavior of breast cancer, and it may be a good molecular therapeutic target to increase the expression level of SIAH1 through promoting cell apoptosis and inhibiting cell invasion in human breast cancer.

Indexed as

ApoptosisMAP Kinase Signaling SystemApoptosis Regulatory ProteinsBcl-2-Like Protein 11Breast NeoplasmsCell Line, TumorExtracellular Signal-Regulated MAP KinasesFemaleHumansJNK Mitogen-Activated Protein KinasesMembrane ProteinsNeoplasm InvasivenessNuclear ProteinsProto-Oncogene ProteinsSeven in Absentia ProteinsUbiquitin-Protein LigasesApoptosis Regulatory ProteinsBCL2L11 protein, humanBcl-2-Like Protein 11Extracellular Signal-Regulated MAP KinasesJNK Mitogen-Activated Protein KinasesMembrane ProteinsNuclear ProteinsProto-Oncogene ProteinsSeven in Absentia ProteinsUbiquitin-Protein Ligases

Identifiers

PMID19775288
PMCPMC11158974
OpenAlexW2036578460

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.