Evidence map›Paper›PMID 27469492›Full record

ArticleScientific reports2016

CD271 regulates the proliferation and motility of hypopharyngeal cancer cells.

Mai Mochizuki, Keiichi Tamai, Takayuki Imai, Sayuri Sugawara, Naoko Ogama, Mao Nakamura, Kazuto Matsuura, Kazunori Yamaguchi, Kennichi Satoh, Ikuro Sato and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

  1. Nerve growth factor receptor (NGFR): A key player in glioblastoma progression.Biochimica et biophysica acta. Reviews on cancer · 2026
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  12. Cell Surface Proteins for Enrichment andStem cells international · 2022
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  13. Article
  14. Cancer stem cells and strategies for targeted drug delivery.Drug delivery and translational research · 2021
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. CD271 is a negative prognostic factor and essential for cell proliferation in lung squamous cell carcinoma.Laboratory investigation; a journal of technical methods and pathology · 2019
    Article
  20. CD271 Confers an Invasive and Metastatic Phenotype of Head and Neck Squamous Cell Carcinoma through the Upregulation of Slug.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
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

13 authors at 2 institutions in 1 country.

Mai MochizukiDivision of Cancer Stem Cell, Miyagi Cancer Center Research Institute, Natori, Japan.
Keiichi TamaiDivision of Cancer Stem Cell, Miyagi Cancer Center Research Institute, Natori, Japan.
Takayuki ImaiDepartment of Head and Neck Surgery, Miyagi Cancer Center, Natori, Japan.
Sayuri SugawaraDivision of Cancer Biology and Therapeutics, Miyagi Cancer Center Research Institute, Natori, Japan.
Naoko OgamaDivision of Cancer Biology and Therapeutics, Miyagi Cancer Center Research Institute, Natori, Japan.
Mao NakamuraMolecular and Cellular Oncology, Miyagi Cancer Center Research Institute, Natori, Japan.
Kazuto MatsuuraDepartment of Head and Neck Surgery, Miyagi Cancer Center, Natori, Japan.
Kazunori YamaguchiMolecular and Cellular Oncology, Miyagi Cancer Center Research Institute, Natori, Japan.
Kennichi SatohDivision of Cancer Stem Cell, Miyagi Cancer Center Research Institute, Natori, Japan.
Ikuro SatoDepartment of Pathology, Miyagi Cancer Center, Natori, Japan.
Hozumi MotohashiDepartment of Gene Expression Regulation, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan.
Kazuo SugamuraMolecular and Cellular Oncology, Miyagi Cancer Center Research Institute, Natori, Japan.
Nobuyuki TanakaDivision of Cancer Biology and Therapeutics, Miyagi Cancer Center Research Institute, Natori, Japan.
Miyagi Prefectural Hospital Organization · JPTohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD271 (p75 neurotrophin receptor) plays both positive and negative roles in cancer development, depending on the cell type. We previously reported that CD271 is a marker for tumor initiation and is correlated with a poor prognosis in human hypopharyngeal cancer (HPC). To clarify the role of CD271 in HPC, we established HPC cell lines and knocked down the CD271 expression using siRNA. We found that CD271-knockdown completely suppressed the cells' tumor-forming capability both in vivo and in vitro. CD271-knockdown also induced cell-cycle arrest in G0 and suppressed ERK phosphorylation. While treatment with an ERK inhibitor only partially inhibited cell growth, CDKN1C, which is required for maintenance of quiescence, was strongly upregulated in CD271-depleted HPC cells, and the double knockdown of CD271 and CDKN1C partially rescued the cells from G0 arrest. In addition, either CD271 depletion or the inhibition of CD271-RhoA signaling by TAT-Pep5 diminished the in vitro migration capability of the HPC cells. Collectively, CD271 initiates tumor formation by increasing the cell proliferation capacity through CDKN1C suppression and ERK-signaling activation, and by accelerating the migration signaling pathway in HPC.

Indexed as

CarcinogenesisCell MovementCell ProliferationCell Line, TumorGene Knockdown TechniquesHumansHypopharyngeal NeoplasmsNerve Tissue ProteinsReceptors, Nerve Growth FactorNerve Tissue ProteinsNGFR protein, humanReceptors, Nerve Growth Factor

Identifiers

PMID27469492
PMCPMC4965829
OpenAlexW2482225679

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.