Evidence map›Paper›PMID 25816351›Full record

ArticlePloS one2015

The differential expression of OCT4 isoforms in cervical carcinoma.

Shao-Wen Li, Xiao-Ling Wu, Chun-Li Dong, Xiu-Ying Xie, Jin-Fang Wu, Xin Zhang

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 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 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

6 authors at 1 institution in 1 country.

Shao-Wen LiDepartment of Pediatrics, the Second Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, China.
Xiao-Ling WuDepartment of Obstetrics and Gynecology, the Second Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, China.
Chun-Li DongDepartment of Obstetrics and Gynecology, the Second Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, China.
Xiu-Ying XieDepartment of Obstetrics and Gynecology, the Second Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, China.
Jin-Fang WuDepartment of Obstetrics and Gynecology, the Second Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, China.
Xin ZhangDepartment of Obstetrics and Gynecology, the Second Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, China.
Second Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OCT4 is a transcription factor involved in maintaining stem cell phenotype and pluripotential. However, it remains unclear the expression pattern and biological function of OCT4 isoforms in cervical cancer. Here, we reported that both nuclear OCT4A and cytoplasmic OCT4B were overexpressed in CC. OCT4A was responsible for self-renewal of cervical cancer stem-like cells (CCSCs). Furthermore, OCT4B overexpression in SiHa cervical cancer cell line significantly increased cell proliferation and tumorigenesis by inhibiting apoptosis. Moreover, OCT4B enhanced angiogenesis by the upregulation of CD34, VEGF, HIF-1α and IL-6, and promoted tumor cell mobility to the surrounding tissue by the upregulation of MMP2 and MMP9, and the induction of epithelial-mesenchymal transition (EMT). In conclusion, nuclear OCT4A may serve as a marker of CCSCs and the driving force for cervical cancer metastasis and recurrence, while cytoplasmic OCT4B may cooperate with OCT4A to regulate the progression of cervical cancer through inducing angiogenesis and EMT.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisCarcinogenesisCell Line, TumorCell ProliferationCell Transformation, NeoplasticFemaleHumansMiceNeovascularization, PathologicOctamer Transcription Factor-3Protein IsoformsUterine Cervical NeoplasmsOctamer Transcription Factor-3POU5F1 protein, humanProtein Isoforms

Identifiers

PMID25816351
PMCPMC4376746
OpenAlexW1987084841

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.