Evidence map›Paper›PMID 30510261›Full record

ArticleScientific reports2018

Crosstalk between SOX2 and cytokine signaling in endometrial carcinoma.

Chang-Jung Lee, Pi-Lin Sung, Ming-Han Kuo, Min-Hwa Tsai, Cheng-Kuang Wang, Shien-Tung Pan, Yi-Jen Chen, Peng-Hui Wang, Kuo-Chang Wen, Yu-Ting Chou

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 27 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

10 authors at 4 institutions in 1 country.

Chang-Jung LeeDepartment of Life Science and Institute of Biotechnology, National Tsing-Hua University, HsinChu, 300, Taiwan (R.O.C.).
Pi-Lin SungDepartment of Obstetrics and Gynecology, Taipei Veterans General Hospital, Taipei, 112, Taiwan (R.O.C.).
Ming-Han KuoDepartment of Life Science and Institute of Biotechnology, National Tsing-Hua University, HsinChu, 300, Taiwan (R.O.C.).
Min-Hwa TsaiDepartment of Life Science and Institute of Biotechnology, National Tsing-Hua University, HsinChu, 300, Taiwan (R.O.C.).
Cheng-Kuang WangDepartment of Medical Technology, Jen-Teh Junior College of Medicine, Nursing and Management, Miaoli, 356, Taiwan (R.O.C.).
Shien-Tung PanDepartment of Pathology, Tungs' Taichung MetroHarbor Hospital, Taichung, 433, Taiwan (R.O.C.).
Yi-Jen ChenDepartment of Obstetrics and Gynecology, Taipei Veterans General Hospital, Taipei, 112, Taiwan (R.O.C.).
Peng-Hui WangDepartment of Obstetrics and Gynecology, Taipei Veterans General Hospital, Taipei, 112, Taiwan (R.O.C.).ORCID http://orcid.org/0000-0002-6048-8541
Kuo-Chang WenDepartment of Obstetrics and Gynecology, Taipei Veterans General Hospital, Taipei, 112, Taiwan (R.O.C.). kcwen@vghtpe.gov.tw.
Yu-Ting ChouDepartment of Life Science and Institute of Biotechnology, National Tsing-Hua University, HsinChu, 300, Taiwan (R.O.C.). ytchou@life.nthu.edu.tw.
National Tsing Hua University · TWNational Yang Ming Chiao Tung University · TWKang-Ning Junior College of Medical Care and Management · TWTungs' Taichung MetroHarbor Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endometrial carcinoma is a cancer derived from oncogenesis of the regenerating uterine cavity, in which cytokine stimulation shapes cell differentiation and tissue remodeling. Expression of the stem cell factors SOX2, OCT4, NANOG, and MYC has been linked to tumor malignancy in several cancers. However, how these stem cell factors crosstalk with cytokine signaling to promote malignancy in endometrial carcinoma is still elusive. Here we report that the expression of SOX2 and MYC, but not that of OCT4 and NANOG, correlate with poor histological differentiation and prognosis, while SOX2 expression is negatively associated with MYC level. We found that SOX2-high endometrial carcinoma cells possessed a higher colony-forming ability than their SOX2-low counterparts, and knockdown of SOX2 attenuated the colony-forming ability. We observed that SOX2 regulated EGFR expression in a SOX2-EGFR positive feedback loop. EGF stimulation induced SOX2 expression and promoted migration of endometrial carcinoma cells, whereas TGF-β stimulation inhibited SOX2 expression and attenuated the colony-forming ability. Immunohistochemistry analysis revealed that SOX2 expression correlated with lymph node infiltration of endometrial carcinoma. Our findings support that cytokine-induced stem cell factor SOX2 possesses oncogenic properties, with the potential to serve as a prognostic biomarker in endometrial carcinoma.

Indexed as

Gene Expression Regulation, NeoplasticBiomarkers, TumorCell Line, TumorCell MovementEndometrial NeoplasmsFemaleHumansProto-Oncogene Proteins c-mycSOXB1 Transcription FactorsBiomarkers, TumorMYC protein, humanProto-Oncogene Proteins c-mycSOX2 protein, humanSOXB1 Transcription Factors

Identifiers

PMID30510261
PMCPMC6277382
OpenAlexW2903363350

What OpenQuestion holds

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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.