Evidence map›Paper›PMID 35034634›Full record

ArticleJournal of biomedical science2022

Estradiol-mediated inhibition of Sp1 decreases miR-3194-5p expression to enhance CD44 expression during lung cancer progression.

Ming-Jer Young, Yung-Ching Chen, Shao-An Wang, Hui-Ping Chang, Wen-Bin Yang, Chia-Chi Lee, Chia-Yu Liu, Yau-Lin Tseng, Yi-Ching Wang, H Sunny Sun and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of biomedical science, 2022. 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
2.0field-weighted citation impact, top 12% 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, 23 citations in OpenAlex.

  1. Review
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  12. Specificity Proteins (Sp) and Cancer.International journal of molecular sciences · 2023
    Review
  13. Review
  14. 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

12 authors at 2 institutions in 1 country.

Ming-Jer Young *Department of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan.
Yung-Ching Chen *Department of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan.
Shao-An WangSchool of Respiratory Therapy, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Hui-Ping ChangDepartment of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan.
Wen-Bin YangTMU Research Center of Neuroscience, Taipei Medical University, 11031, Taipei, Taiwan.
Chia-Chi LeeDivision of Thoracic Surgery, Department of Surgery, College of Medicine National, Cheng Kung University, Tainan, Taiwan.
Chia-Yu LiuDepartment of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan.
Yau-Lin TsengDivision of Thoracic Surgery, Department of Surgery, College of Medicine National, Cheng Kung University, Tainan, Taiwan.
Yi-Ching WangDepartment of Pharmacology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
H Sunny SunInstitute of Molecular Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Wen-Chang ChangThe Ph.D. Program for Neural Regenerative Medicine, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
Jan-Jong HungDepartment of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan. petehung@mail.ncku.edu.tw.ORCID http://orcid.org/0000-0001-5772-8877
National Cheng Kung University · TWTaipei Medical University · TW

Funding

Ministry of Science and Technology, Taiwan 106-2320-B-006-065-MY3Ministry of Science and Technology, Taiwan 108-2320-B-006-019Ministry of Science and Technology, Taiwan 109-2320-B-006-057
6 · The paper itself

Abstract

backgroundSp1, an important transcription factor, is involved in the progression of various cancers. Our previous studies have indicated that Sp1 levels are increased in the early stage of lung cancer progression but decrease during the late stage, leading to poor prognosis. In addition, estrogen has been shown to be involved in lung cancer progression. According to previous studies, Sp1 can interact with the estrogen receptor (ER) to coregulate gene expression. The role of interaction between Sp1 and ER in lung cancer progression is still unknown and will be clarified in this study.

methodsThe clinical relevance between Sp1 levels and survival rates in young women with lung cancer was studied by immunohistochemistry. We validated the sex dependence of lung cancer progression in EGFR

resultsIn this study, we found that Sp1 expression was decreased in premenopausal women with late-stage lung cancer, resulting in a poor prognosis. Tumor formation was more substantial in female EGFR

conclusionPremenopausal women with lung cancer and decreased Sp1 levels have a poor prognosis. E2 increases RNF4 expression to repress Sp1 levels in premenopausal women with lung cancer, thus decreasing the expression of several miRNAs that can target CD44 and ultimately leading to cancer malignancy.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsMicroRNAsA549 CellsAnimalsCell Line, TumorCell ProliferationEstradiolFemaleHumansHyaluronan ReceptorsMaleMiceNuclear ProteinsSp1 Transcription FactorTranscription FactorsCD44 protein, humanEstradiolHyaluronan ReceptorsMicroRNAsMIRN218 microRNA, humanNuclear ProteinsRNF4 protein, humanSP1 protein, humanSp1 Transcription FactorTranscription FactorsCD44Estradiol (E2)Lung cancermicroRNAsRNF4Sp1

Identifiers

PMID35034634
PMCPMC8762881
OpenAlexW4206025390

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.