Evidence map›Paper›PMID 25594044›Full record

ArticleOncoscience2014

Effects of octreotide and insulin on colon cancer cellular proliferation and correlation with hTERT activity.

Georgios D Ayiomamitis, George Notas, Apostolos Zaravinos, Ioannis Drygiannakis, Maria Georgiadou, Ourania Sfakianaki, Niki Mastrodimou, Kyriaki Thermos, Elias Kouroumalis

Open access · hybridAbstract read
In one paragraph

Article in Oncoscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

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  8. Preclinical study of a newAsia Oceania journal of nuclear medicine & biology · 2020
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  12. Article
  13. Up-regulation of NHE8 by somatostatin ameliorates the diarrhea symptom in infectious colitis mice model.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2018
    Article
  14. Telomerase: a target for colorectal cancer treatment?Cell cycle (Georgetown, Tex.) · 2015
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 2 countries.

Georgios D AyiomamitisLaboratory of Gastroenterology, School of Medicine, University of Crete, Heraklion, Greece ; 2nd Department of Surgery, Tzaneion General Hospital, Piraeus, Greece.
George NotasLaboratory of Gastroenterology, School of Medicine, University of Crete, Heraklion, Greece ; Laboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Apostolos ZaravinosLaboratory of Clinical Virology, School of Medicine, University of Crete, Heraklion, Greece ; Department of Laboratory Medicine, Karolinska Institute, Stockholm, Sweden.
Ioannis DrygiannakisLaboratory of Gastroenterology, School of Medicine, University of Crete, Heraklion, Greece.
Maria GeorgiadouLaboratory of Gastroenterology, School of Medicine, University of Crete, Heraklion, Greece.
Ourania SfakianakiLaboratory of Gastroenterology, School of Medicine, University of Crete, Heraklion, Greece.
Niki MastrodimouLaboratory of Pharmacology, School of Medicine, University of Crete, Heraklion, Crete, Greece.
Kyriaki ThermosLaboratory of Pharmacology, School of Medicine, University of Crete, Heraklion, Crete, Greece.
Elias KouroumalisLaboratory of Gastroenterology, School of Medicine, University of Crete, Heraklion, Greece ; Department of Gastroenterology and Hepatology, School of Medicine, University of Crete, Heraklion, Greece.
University of Crete · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peptide hormone somatostatin and its receptors have a wide range of physiological functions and play a role in the treatment of numerous human diseases, including colorectal cancer. Octreotide, a synthetic somatostatin-analog peptide, inhibits growth of colonic cancer cells primarily by binding to G-protein coupled receptors and elicits cellular responses through second-messenger systems. Insulin also initiates mitogenic signals in certain cell types. The objective of the present study was to explore the effects of octreotide with or without insulin treatment, on Caco-2 and HT-29 human colon-cancer cell proliferation and to correlate their effects with the activation of telomerase reverse transcriptase (hTERT). The involvement of protein tyrosine phosphatases in the regulation of the anti-proliferative effect of octreotide was also evaluated. Sodium orthovanadate was used to reverse the anti- proliferative effect of octreotide. Telomerase activity was determined for each time point under octreotide and/or insulin treatment. Elevated expression of sst1, sst2 and sst5 was confirmed in both cell lines by RT-PCR. Immunocytochemistry detected sst1, sst2A, sst2B, sst3, sst4 and sst5 protein expression in the membranes of both cell lines. Octreotide inhibited the proliferation of Caco-2 and HT-29 cells in a time and dose-dependent manner. Insulin exerted proliferative effects in Caco-2 cells and octreotide reversed its effect in both cell lines. Sodium orthovanadate suppressed the anti-proliferative effect of octreotide both in Caco-2 and HT-29 cells. Telomerase activity was significantly reduced when Caco-2 cells were exposed to octreotide, under serum-free cultured medium. On the other hand, telomerase attenuation after octreotide treatment could not counteract the actions of insulin on both cells. Our data indicate that the use of octreotide could provide a possible therapeutic approach to the management of certain patients who suffer from colon cancer.

Indexed as

colorectal cancerhTERT activityinsulinOctreotideprotein tyrosine phosphatasessodium orthovanadate

Identifiers

PMID25594044
PMCPMC4284627
OpenAlexW2111811103

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.