Evidence map›Paper›PMID 26918356›Full record

ArticleOncotarget2016

Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients.

Bharath Kumar Velmurugan, Kun-Tu Yeh, Chien-Hung Lee, Shu-Hui Lin, Mei-Chung Chin, Shang-Lun Chiang, Zhi-Hong Wang, Chun-Hung Hua, Ming-Hsui Tsai, Jan-Gowth Chang and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. 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
1.3field-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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. [Silenced ANP32A inhibits the growth, invasion and migration of colorectal cancerNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
  3. Article
  4. Gga-miR-181a modulates ANP32A expression and inhibits MDCC-MSB-1 cell.In vitro cellular & developmental biology. Animal · 2021
    Article
  5. B Cells Improve Overall Survival in HPV-Associated Squamous Cell Carcinomas and Are Activated by Radiation and PD-1 Blockade.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. 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

11 authors at 5 institutions in 1 country.

Bharath Kumar VelmuruganEnvironment-Omics-Diseases Research, China Medical University Hospital, Taichung, Taiwan.
Kun-Tu YehDepartment of Pathology, Changhua Christian Hospital, Changhua, Taiwan.
Chien-Hung LeeDepartment of Public Health, College of Health Science, Kaohsiung Medical University, Kaohsiung, Taiwan.
Shu-Hui LinDepartment of Pathology, Changhua Christian Hospital, Changhua, Taiwan.
Mei-Chung ChinDepartment of Pathology, Changhua Christian Hospital, Changhua, Taiwan.
Shang-Lun ChiangEnvironment-Omics-Diseases Research, China Medical University Hospital, Taichung, Taiwan.
Zhi-Hong WangEnvironment-Omics-Diseases Research, China Medical University Hospital, Taichung, Taiwan.
Chun-Hung HuaDepartment of Otorhinolaryngology, China Medical University Hospital, Taichung, Taiwan.
Ming-Hsui TsaiDepartment of Otorhinolaryngology, China Medical University Hospital, Taichung, Taiwan.
Jan-Gowth ChangDepartment of Laboratory Medicine, China Medical University Hospital, Taichung, Taiwan.
Ying-Chin KoEnvironment-Omics-Diseases Research, China Medical University Hospital, Taichung, Taiwan.
China Medical University Hospital · TWChina Medical University · TWChung Shan Medical University · TWChanghua Christian Hospital · TWKaohsiung Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) is a multifunctional protein aberrantly expressed in various types of cancers. However, its expression pattern and clinical significance in oral squamous cell carcinoma (OSCC) remains unclear. In this study, we immunohistochemically investigated the expression pattern of ANP32A in 259 OSCC patients and the results were correlated with clinicopathological factors using Allred, Klein and Immunoreactive scoring (IRS) system. Our data indicated that high expression of ANP32A was significantly associated with N stage and tumor differentiation status in OSCC patients. High ANP32A expression with N2/N3 stage had an increased mortality risk than low ANP32A expressing OSCC patients with N0/N1 stage. Functional studies revealed that knockdown of ANP32A significantly decreased the migration and invasion ability thereby concomitantly increasing E-cadherin and decreasing Slug, Claudin-1 and Vimentin expression in vitro. These results suggest that ANP32A is commonly increased in oral squamous cell carcinoma and ANP32A protein could act as a potential biomarker for prognosis assessment of oral cancer patients with lymph node metastasis.

Indexed as

AgedBiomarkers, TumorCarcinoma, Squamous CellCell MovementClaudin-1FemaleHead and Neck NeoplasmsHumansImmunohistochemistryIntracellular Signaling Peptides and ProteinsLymphatic MetastasisMiddle AgedMouth NeoplasmsNuclear ProteinsPrognosisRNA-Binding ProteinsANP32A protein, humanBiomarkers, TumorClaudin-1CLDN1 protein, humanIntracellular Signaling Peptides and ProteinsNuclear ProteinsRNA-Binding ProteinsVimentinANP32AClaudlin-1EMTOSCCPathology SectionSlug

Identifiers

PMID26918356
PMCPMC4905446
OpenAlexW2292031391

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.