Evidence map›Paper›PMID 26053695›Full record

ArticlePloS one2015

The Characteristics and Function of S100A7 Induction in Squamous Cell Carcinoma: Heterogeneity, Promotion of Cell Proliferation and Suppression of Differentiation.

Zhi Qi, Ting Li, Fei Kong, Yunguang Li, Rui Wang, Junhao Wang, Qianqian Xiao, Weiqing Zhang, Suozhu Sun, Dacheng He and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 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
1.5field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Zhi QiKey laboratory of Cell Proliferation and Regulation of Ministry of Education, Beijing Normal University, Beijing, China.
Ting LiKey laboratory of Cell Proliferation and Regulation of Ministry of Education, Beijing Normal University, Beijing, China.
Fei KongKey laboratory of Cell Proliferation and Regulation of Ministry of Education, Beijing Normal University, Beijing, China.
Yunguang LiKey laboratory of Cell Proliferation and Regulation of Ministry of Education, Beijing Normal University, Beijing, China.
Rui WangKey laboratory of Cell Proliferation and Regulation of Ministry of Education, Beijing Normal University, Beijing, China.
Junhao WangKey laboratory of Cell Proliferation and Regulation of Ministry of Education, Beijing Normal University, Beijing, China.
Qianqian XiaoKey laboratory of Cell Proliferation and Regulation of Ministry of Education, Beijing Normal University, Beijing, China.
Weiqing ZhangKey laboratory of Cell Proliferation and Regulation of Ministry of Education, Beijing Normal University, Beijing, China.
Suozhu SunKey laboratory of Cell Proliferation and Regulation of Ministry of Education, Beijing Normal University, Beijing, China; Department of Pathology, General Hospital of the Second Artillery, Beijing, China.
Dacheng HeUniversities' Confederated Institute of Proteomics, Beijing, China.
Xueyuan XiaoKey laboratory of Cell Proliferation and Regulation of Ministry of Education, Beijing Normal University, Beijing, China.
Beijing Normal University · CNBeijing Proteome Research Center · CNSecond Artillery General Hospital of Chinese People's Liberation Army · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

S100A7 is highly expressed in squamous cell carcinomas (SCC) and is related to the terminal differentiation of keratinocytes. However, its characteristic and function in SCC is not very known. In this present study, we used immunohistochemistry to examine the expression of S100A7 in 452 SCC specimens, including the lung, esophagus, oral cavity, skin, cervix, bladder, and three SCC cell lines. We found that S100A7-positive staining showed significant heterogeneity in six types of SCC specimen and three SCC cell lines. Further examination found that S100A7-positive cells and its expression at mRNA and protein levels could be induced in HCC94, FaDu, and A-431 cells both in vitro and in vivo using immunohistochemistry, real-time PCR, and Western blotting. Notably, the upregulation of squamous differentiation markers, including keratin-4, keratin-13, TG-1, and involucrin, also accompanied S100A7 induction, and a similar staining pattern of S100A7 and keratin-13 was found in HCC94 cells both in vitro and in vivo. Further study revealed that the overexpression of S100A7 significantly increased proliferation and inhibited squamous differentiation in A-431 cells both in vitro and in vivo. Conversely, silencing S100A7 inhibited cell growth and survival and increased the expression of keratin-4, keratin-13, TG-1, and involucrin in HCC94 cells. Therefore, these results demonstrate that S100A7 displays heterogeneous and inducible characteristic in SCC and also provide novel evidence that S100A7 acts as a dual regulator in promoting proliferation and suppressing squamous differentiation of SCC.

Indexed as

Cell DifferentiationAnimalsBiomarkers, TumorCarcinoma, Squamous CellCell Line, TumorCell ProliferationCell SurvivalHumansImmunohistochemistryKeratin-13Mice, Inbred BALB CMice, NudeS100 Calcium Binding Protein A7S100 ProteinsSuspensionsXenograft Model Antitumor AssaysBiomarkers, TumorKeratin-13KRT13 protein, humanS100A7 protein, humanS100 Calcium Binding Protein A7S100 ProteinsSuspensions

Identifiers

PMID26053695
PMCPMC4460013
OpenAlexW1907937493

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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.