Evidence map›Paper›PMID 24817940›Full record

ArticleInternational journal of clinical and experimental pathology2014

AKT/ERK activation is associated with gastric cancer cell resistance to paclitaxel.

Gang Wu, Xue-Qian Qin, Jing-Jing Guo, Tian-Yi Li, Jin-Hong Chen

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
  6. Non-coding RNA in drug resistance of gastric cancer.World journal of gastrointestinal oncology · 2019
    Review
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  14. [Expression of cAMP-dependent protein kinase inhibitor beta in colorectal carcinoma and its clinical significance].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2017
    Article
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  20. The α7-nicotinic acetylcholine receptor mediates the sensitivity of gastric cancer cells to taxanes.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    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 2 institutions in 1 country.

Gang WuDepartment of General Surgery, Huashan Hospital, Fudan University Shanghai 200040, China ; Department of General Surgery, Renhe Hospital Baoshan District, Shanghai 20043, China.
Xue-Qian QinDepartment of General Surgery, Renhe Hospital Baoshan District, Shanghai 20043, China.
Jing-Jing GuoDepartment of General Surgery, Renhe Hospital Baoshan District, Shanghai 20043, China.
Tian-Yi LiDepartment of General Surgery, Huashan Hospital, Fudan University Shanghai 200040, China.
Jin-Hong ChenDepartment of General Surgery, Huashan Hospital, Fudan University Shanghai 200040, China.
Huashan Hospital · CNRenji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paclitaxel (PTX) has shown encouraging activity in the treatment of advanced gastric cancer (GC). However, the fact that more than half of GC patients respond poorly to PTX-based chemotherapies demonstrates the urgent need for biomarkers of PTX sensitivity in GC patients. In the present work, three GC cell lines (BGC-823, HGC-27 and NCI-N87) with different sensitivities to PTX were subjected to DNA microarray analysis. The significantly differentially expressed genes and microRNAs (miRs) were identified and pathway signatures for PTX sensitivity were proposed. Ingenuity Pathway Analysis results showed that the differentially expressed genes were mainly enriched in the ErbB signaling pathway and other pathways. Additionally, the AKT/ERK signaling pathway, which is the pathway downstream of ErbB, was predicted to be active in PTX-resistant GC cell lines. ErbB3 overexpression and AKT/ERK activation in PTX-resistant cell lines were validated, respectively, by quantitative PCR and immunoblotting. Furthermore, 10 miRs were dramatically differently expressed in the three GC cell lines, and a miR-gene network was constructed from these data. Our work uncovered a reliable signature for PTX sensitivity in GC and potential therapeutic targets for GC treatments.

Indexed as

AdenocarcinomaAntineoplastic Agents, PhytogenicApoptosisCell Line, TumorDrug Resistance, NeoplasmExtracellular Signal-Regulated MAP KinasesGene Expression Regulation, NeoplasticHumansOligonucleotide Array Sequence AnalysisOncogene Proteins v-erbBPaclitaxelProto-Oncogene Proteins c-aktSignal TransductionStomach NeoplasmsTreatment FailureAntineoplastic Agents, PhytogenicExtracellular Signal-Regulated MAP KinasesOncogene Proteins v-erbBPaclitaxelProto-Oncogene Proteins c-aktAKT signalingDNA microarrayErbB signalingERK signalingGastric cancermicroRNApaclitaxel

Identifiers

PMID24817940
PMCPMC4014224
OpenAlexW75787445

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.