Evidence map›Paper›PMID 31019292›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2019

CD271 is a negative prognostic factor and essential for cell proliferation in lung squamous cell carcinoma.

Mai Mochizuki, Mao Nakamura, Rie Sibuya, Toshimasa Okazaki, Jiro Abe, Takayuki Nakagawa, Satomi Takahashi, Tomoko Yamazaki, Takayuki Imai, Atsushi Takano and 9 more

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In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 13 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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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

19 authors at 3 institutions in 1 country.

Mai MochizukiDivision of Cancer Stem Cell, Miyagi Cancer Center Research Institute, Natori, Japan.
Mao NakamuraDivision of Molecular and Cellular Oncology, Miyagi Cancer Center Research Institute, Natori, Japan.
Rie SibuyaDivision of Cancer Stem Cell, Miyagi Cancer Center Research Institute, Natori, Japan.
Toshimasa OkazakiDepartment of Thoracic Surgery, Miyagi Cancer Center, Natori, Japan.
Jiro AbeDepartment of Thoracic Surgery, Miyagi Cancer Center, Natori, Japan.
Takayuki NakagawaDivision of Cancer Stem Cell, Miyagi Cancer Center Research Institute, Natori, Japan.
Satomi TakahashiDepartment of Thoracic Surgery, Miyagi Cancer Center, Natori, Japan.
Tomoko YamazakiDepartment of Head and Neck Medical Oncology, Miyagi Cancer Center, Natori, Japan.
Takayuki ImaiDepartment of Head and Neck Surgery, Miyagi Cancer Center, Natori, Japan.
Atsushi TakanoCenter for Antibody and Vaccine Therapy, Research Hospital, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Hiroyuki ItoDepartment of Thoracic Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Tomoyuki YokoseDepartment of Pathology, Kanagawa Cancer Center, Yokohama, Japan.ORCID http://orcid.org/0000-0002-9403-9592
Yohei MiyagiMolecular Pathology and Genetics Division, Kanagawa Cancer Center Research Institute, Yokohama, Japan.
Yataro DaigoCenter for Antibody and Vaccine Therapy, Research Hospital, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Ikuro SatoDepartment of Pathology, Miyagi Cancer Center, Natori, Japan.
Kennichi SatohDivision of Cancer Stem Cell, Miyagi Cancer Center Research Institute, Natori, Japan.
Kazuo SugamuraDivision of Molecular and Cellular Oncology, Miyagi Cancer Center Research Institute, Natori, Japan.
Kazunori YamaguchiDivision of Molecular and Cellular Oncology, Miyagi Cancer Center Research Institute, Natori, Japan.
Keiichi TamaiDivision of Cancer Stem Cell, Miyagi Cancer Center Research Institute, Natori, Japan. tamaikeiichi@med.tohoku.ac.jp.
Miyagi Prefectural Hospital Organization · JPKanagawa Prefectural Hospital Organization · JPShiga University of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Squamous cell carcinoma is a major type of cancer in the lung. While several therapeutic target molecules for lung adenocarcinoma have been identified, little is known about lung squamous cell carcinoma (LSCC). We recently reported that CD271 (p75 neurotrophin receptor) serves as a marker for tumor initiation and is a key regulator of cell proliferation in hypopharyngeal squamous cell carcinoma. In this study, we found that CD271 was also expressed in squamous cell carcinoma, but not in adenocarcinoma, of several tissues, including the lung, and the expression of CD271 was associated with a poor prognosis in LSCC. To examine CD271's role in LSCC, we established xenograft cell lines from LSCC patients. Within the sorted live LSCC cell population, the CD271

Indexed as

Nerve Tissue ProteinsReceptors, Nerve Growth FactorAgedAged, 80 and overAnimalsBiomarkers, TumorCarcinoma, Squamous CellCell Line, TumorCell MovementCell ProliferationDisease-Free SurvivalFemaleHumansLung NeoplasmsMaleMice, Inbred NODBiomarkers, TumorNerve Tissue ProteinsNGFR protein, humanReceptors, Nerve Growth Factor

Identifiers

PMID31019292
OpenAlexW2941591292

What OpenQuestion holds

Textmetadata
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.