Evidence map›Paper›PMID 24619193›Full record

ArticleInternational journal of molecular sciences2014

Synergistic enhancement of cancer therapy using a combination of ceramide and docetaxel.

Li-Xia Feng, Min Li, Yong-Jun Liu, Shao-Mei Yang, Na Zhang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-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

16 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  4. The Conjugates of Indolo[2,3-International journal of molecular sciences · 2024
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  7. Synergistic cytotoxicity of perifosine and ABT-737 to colon cancer cells.Journal of cellular and molecular medicine · 2023
    Article
  8. Article
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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.

Li-Xia FengDepartment of Pharmaceutics, College of Pharmacy, Shandong University, 44 West Culture Road, Ji'nan 250012, China. fenglixia0910@126.com.
Min LiDepartment of Pharmaceutics, College of Pharmacy, Shandong University, 44 West Culture Road, Ji'nan 250012, China. sdlimin@sina.cn.
Yong-Jun LiuDepartment of Pharmaceutics, College of Pharmacy, Shandong University, 44 West Culture Road, Ji'nan 250012, China. o-oliuyongjun@163.com.
Shao-Mei YangDepartment of Pharmaceutics, College of Pharmacy, Shandong University, 44 West Culture Road, Ji'nan 250012, China. yangshaomei01@163.com.
Na ZhangDepartment of Pharmaceutics, College of Pharmacy, Shandong University, 44 West Culture Road, Ji'nan 250012, China. zhangnancy9@sdu.edu.cn.
Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ceramide (CE)-based combination therapy (CE combination) as a novel therapeutic strategy has attracted great attention in the field of anti-cancer therapy. The principal purposes of this study were to investigate the synergistic effect of CE in combination with docetaxel (DTX) (CE + DTX) and to explore the synergy mechanisms of CE + DTX. The 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and combination index (CI) assay showed that simultaneous administration of CE and DTX with a molar ratio of 0.5:1 could generate the optimal synergistic effect on murine malignant melanoma cell (B16, CI = 0.31) and human breast carcinoma cell (MCF-7, CI = 0.48). The apoptosis, cell cycle, and cytoskeleton destruction study demonstrated that CE could target and destruct the microfilament actin, subsequently activate Caspase-3 and induce apoptosis. Meanwhile, DTX could target and disrupt the microtubules cytoskeleton, leading to a high proportion of cancer cells in G2/M-phase arrest. Moreover, CE plus DTX could cause a synergistic destruction of cytoskeleton, which resulted in a significantly higher apoptosis and a significantly higher arrest in G2/M arrest comparing with either agent alone (p < 0.01). The in vivo antitumor study evaluated in B16 tumor-bearing mice also validated the synergistic effects. All these results suggested that CE could enhance the antitumor activity of DTX in a synergistic manner, which suggest promising application prospects of CE + DTX combination treatment.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsApoptosisCaspase 3Cell Line, TumorCell ProliferationCell SurvivalCeramidesCytoskeletonDocetaxelDose-Response Relationship, DrugDrug SynergismFemaleG2 Phase Cell Cycle CheckpointsHep G2 CellsHumansCaspase 3CeramidesDocetaxelTaxoids

Identifiers

PMID24619193
PMCPMC3975392
OpenAlexW2152352667

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.