Evidence map›Paper›PMID 26528857›Full record

ArticleOncotarget2015

ILs-3, 6 and 11 increase, but ILs-10 and 24 decrease stemness of human prostate cancer cells in vitro.

Dandan Yu, Yali Zhong, Xiaoran Li, Yaqing Li, Xiaoli Li, Jing Cao, Huijie Fan, Yuan Yuan, Zhenyu Ji, Baoping Qiao and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
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  8. Article
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  12. Interleukin 6 promotes anRoyal Society open science · 2018
    Article
  13. Oncotarget · 2017
    Article
  14. 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

15 authors at 5 institutions in 2 countries.

Dandan YuDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
Yali ZhongDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
Xiaoran LiDepartment of Pathology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.
Yaqing LiDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
Xiaoli LiDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
Jing CaoDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
Huijie FanDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
Yuan YuanDepartment of Pathology, Capital Medical University, Beijing, China.
Zhenyu JiDepartment of Oncology, Henan Academy of Medical & Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, China.
Baoping QiaoDepartment of Urodynamic Center and Urology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
Jian-Guo WenDepartment of Urodynamic Center and Urology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
Mingzhi ZhangDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
Gunnar KvalheimDepartment of Cell Therapy, Cancer Institute, Radium Hospital, Oslo University Hospital, Oslo, Norway.
Jahn M NeslandDepartment of Pathology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.
Zhenhe SuoDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Henan, China.
First Affiliated Hospital of Zhengzhou University · CNOslo University Hospital · NOCapital Medical University · CNUniversity of Oslo · NOZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer stem cells (CSCs) are associated with cancer recurrence and metastasis. Prostate cancer cells often metastasize to the bone with a complex microenvironment of cytokines favoring cell survival. In this study, the cell stemness influence of a group of interleukins including IL-3, 6, 10, 11 and 24 on human prostate cancer cell lines LNCaP and PC-3 was explored in vitro. Sulforhodamine B(SRB) and 5-ethynyl-2'-deoxyuridine (EdU) assays were applied to examine the effect on cell proliferation, and wound healing and transwell assays were used for migration and invasion studies, in addition to colony formation, Western blotting and flowcytometry for the expression of stemness factors and chemotherapy sensitivity. We observed that ILs-3, 6 and 11 stimulated while ILs-10 and 24 inhibited the growth, invasion and migration of both cell lines. Interestingly, ILs-3, 6 and 11 significantly promoted colony formation and increased the expression of SOX2, CD44 and ABCG2 in both prostate cancer cell lines. However, ILs-10 and 24 showed the opposite effect on the expression of these factors. In line with the above findings, treatment with either IL-3 or IL-6 or IL-11 decreased the chemosensitivity to docetaxel while treatment with either IL-10 or IL-24 increased the sensitivity of docetaxel chemotherapy. In conclusion, our results suggest that ILs-3, 6 and 11 function as tumor promoters while ILs-10 and 24 function as tumor suppressors in the prostate cancer cell lines PC-3 and LNCaP in vitro, and such differences may attribute to their different effect on the stemness of PCa cells.

Indexed as

Blotting, WesternCell Line, TumorCell MovementCell ProliferationDrug Resistance, NeoplasmFlow CytometryGene Expression Regulation, NeoplasticHumansInterleukin-10Interleukin-11Interleukin-24Interleukin-3Interleukin-6InterleukinsIn Vitro TechniquesMaleIL10 protein, humanIL11 protein, humanIL3 protein, humanIL6 protein, humanInterleukin-10Interleukin-11Interleukin-24Interleukin-3Interleukin-6Interleukinscancer stem cellsCD44 and ABCG2chemotherapycytokinesinterleukin

Identifiers

PMID26528857
PMCPMC4767463
OpenAlexW1904535000

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.