Evidence map›Paper›PMID 26315028›Full record

ArticleBMC cancer2015

Gamma tocotrienol targets tyrosine phosphatase SHP2 in mammospheres resulting in cell death through RAS/ERK pathway.

Wenyi Gu, Indira Prasadam, Meihua Yu, Fengxia Zhang, Patrick Ling, Yin Xiao, Chengzhong Yu

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact, top 98% 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

11 citing papers in PubMed, 0 citations in OpenAlex.

  1. Review
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  5. Inhibition of colon cancer K-RasFrontiers in pharmacology · 2022
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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

7 authors at 2 institutions in 1 country.

Wenyi GuAustralian Institute for Bioengineering and Nanotechnology, the University of Queensland, The corner of Cooper Rd. St Lucia, Brisbane, QLD 4072, Australia. w.gu@uq.edu.au.
Indira PrasadamInstitute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Australia. i.prasadam@qut.edu.au.
Meihua YuAustralian Institute for Bioengineering and Nanotechnology, the University of Queensland, The corner of Cooper Rd. St Lucia, Brisbane, QLD 4072, Australia. m.yu2@uq.edu.au.
Fengxia ZhangSchool of Biomedical Science, the University of Queensland, Brisbane, Australia. fengxia.zhang@uqconnect.edu.au.
Patrick LingInstitute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Australia. mingtat.ling@qut.edu.au.
Yin XiaoInstitute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Australia. yin.xiao@qut.edu.au.
Chengzhong YuAustralian Institute for Bioengineering and Nanotechnology, the University of Queensland, The corner of Cooper Rd. St Lucia, Brisbane, QLD 4072, Australia. c.yu@uq.eud.au.
University of Queensland · AUQueensland University of Technology · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is increasing evidence supporting the concept of cancer stem cells (CSCs), which are responsible for the initiation, growth and metastasis of tumors. CSCs are thus considered the target for future cancer therapies. To achieve this goal, identifying potential therapeutic targets for CSCs is essential.

methodsWe used a natural product of vitamin E, gamma tocotrienol (gamma-T3), to treat mammospheres and spheres from colon and cervical cancers. Western blotting and real-time RT-PCR were employed to identify the gene and protein targets of gamma-T3 in mammospheres.

resultsWe found that mammosphere growth was inhibited in a dose dependent manner, with total inhibition at high doses. Gamma-T3 also inhibited sphere growth in two other human epithelial cancers, colon and cervix. Our results suggested that both Src homology 2 domain-containing phosphatase 1 (SHP1) and 2 (SHP2) were affected by gamma-T3 which was accompanied by a decrease in K- and H-Ras gene expression and phosphorylated ERK protein levels in a dose dependent way. In contrast, expression of self-renewal genes TGF-beta and LIF, as well as ESR signal pathways were not affected by the treatment. These results suggest that gamma-T3 specifically targets SHP2 and the RAS/ERK signaling pathway.

conclusionsSHP1 and SHP2 are potential therapeutic targets for breast CSCs and gamma-T3 is a promising natural drug for future breast cancer therapy.

Indexed as

AntioxidantsBlotting, WesternBreast NeoplasmsCell DeathCell Line, TumorChromansColonic NeoplasmsExtracellular Signal-Regulated MAP KinasesFemaleFlow CytometryHumansMicroscopy, FluorescenceProtein Tyrosine Phosphatase, Non-Receptor Type 11ras ProteinsReal-Time Polymerase Chain ReactionSignal TransductionAntioxidantsChromansExtracellular Signal-Regulated MAP Kinasesplastochromanol 8Protein Tyrosine Phosphatase, Non-Receptor Type 11ras ProteinsVitamin E

Identifiers

PMID26315028
PMCPMC4552156
OpenAlexW1522972590

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.