Evidence map›Paper›PMID 26134785›Full record

ArticleMolecular medicine reports2015

Aberrant Wnt/β-catenin signaling and elevated expression of stem cell proteins are associated with osteosarcoma side population cells of high tumorigenicity.

Xi-Jun Yi, Yu-Hua Zhao, Li-Xiang Qiao, Chun-Lei Jin, Jing Tian, Qiu-Shi Li

Abstract read
In one paragraph

Article in Molecular medicine reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. TREX1 suppression imparts cancer-stem-cell-like characteristics to CD133International journal of clinical and experimental pathology · 2019
    Article
  10. Article
  11. Review
  12. [Clinical significance of CD44 and CD133 expression in oral potentially malignant disorder and oral squamous cell carcinoma].Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2017
    Article
  13. Article
  14. Review
  15. Review
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

6 authors.

Xi-Jun YiDepartment of Traumatology, Linyi People's Hospital, Linyi, Shandong 276000, P.R. China.
Yu-Hua ZhaoDepartment of Traumatology, Linyi People's Hospital, Linyi, Shandong 276000, P.R. China.
Li-Xiang QiaoDepartment of Traumatology, Linyi People's Hospital, Linyi, Shandong 276000, P.R. China.
Chun-Lei JinDepartment of Traumatology, Linyi People's Hospital, Linyi, Shandong 276000, P.R. China.
Jing TianOperating Room, Linyi Cancer Hospital, Linyi, Shandong 276000, P.R. China.
Qiu-Shi LiDepartment of Traumatology, Linyi People's Hospital, Linyi, Shandong 276000, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

According to the cancer stem cell theory, the presence of a small sub‑population of cancer cells, termed cancer stem cells (CSCs), have a significant implication on cancer treatment and are responsible for tumor recurrence. Previous studies have reported that alterations in the Wnt/β‑catenin signaling are crucial in the maintenance of CSCs. In the present study, the characteristic features and activation of Wnt/β‑catenin signaling in CSCs from osteosarcoma, an aggressive human bone tumor, were investigated. In total, ~2.1% of the cancer stem‑like side population (SP) cells were identified in the osteosarcoma samples. The results of subsequent western blot and reverse transcription‑quantitative polymerase chain reaction analyses revealed that the protein levels of β‑catenin and cyclin D1 were markedly upregulated in the fluorescence‑activated cell sorted osteosarcoma SP cells. In addition, the elevated expression levels of stem cell proteins, including CD133, nestin Oct‑4, Sox‑2 and Nanog were significantly higher in the SP cells, which contributed to self‑renewal and enhanced the proliferation rate of the SP cells. Furthermore, the SP cells were found to be highly invasive and able to form tumors in vivo. Taken together, these data suggested that the identification of novel anticancer drugs, which suppress the Wnt/β‑catenin signaling and its downstream pathway may assist in eradicating osteosarcoma stem cells.

Indexed as

Gene Expression Regulation, NeoplasticWnt Signaling PathwayAC133 AntigenAdultAnimalsAntigens, CDAntineoplastic Agentsbeta CateninBone NeoplasmsCyclin D1Drug Resistance, NeoplasmFemaleGlycoproteinsHomeodomain ProteinsHumansMaleAC133 AntigenAntigens, CDAntineoplastic Agentsbeta CateninCCND1 protein, humanCTNNB1 protein, humanCyclin D1GlycoproteinsHomeodomain ProteinsNanog Homeobox ProteinNANOG protein, humanOctamer Transcription Factor-3PeptidesPOU5F1 protein, humanPROM1 protein, humanProm1 protein, mouseSOX2 protein, humanSOXB1 Transcription Factors

Identifiers

PMID26134785
PMCPMC4581745

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Registered trials

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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.