Evidence map›Paper›PMID 36151071›Full record

ArticleCell death & disease2022

miR-138-5p-mediated HOXD11 promotes cell invasion and metastasis by activating the FN1/MMP2/MMP9 pathway and predicts poor prognosis in penile squamous cell carcinoma.

Xingliang Tan, Zhenhua Liu, Yanjun Wang, Zhiming Wu, Yuantao Zou, Sihao Luo, Yi Tang, Dong Chen, Gangjun Yuan, Kai Yao

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

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  7. Review
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  9. Article
  10. Article
  11. Article
  12. The Role of miR-138 in Cardiovascular Diseases.BioMed research international · 2025
    Review
  13. The Role of Redox Environment in Tumors.Current medicinal chemistry · 2025
    Review
  14. Article
  15. Article
  16. Article
  17. Review
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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 2 institutions in 1 country.

Xingliang Tan *Department of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China.ORCID 0000-0002-4015-4982
Zhenhua Liu *Department of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Yanjun Wang *Department of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Zhiming Wu *Department of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Yuantao ZouDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Sihao LuoDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Yi TangDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Dong ChenDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China. chendong1@sysucc.org.cn.
Gangjun YuanDepartment of Urology Oncological Surgery, Chongqing University Cancer Hospital, Chongqing, China. yuangj@cqu.edu.cn.
Kai YaoDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China. yaokai@sysucc.org.cn.ORCID 0000-0002-2589-3058
Sun Yat-sen University · CNChongqing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence and extent of regional lymph node and distant metastasis are the most fatal prognostic factors in penile squamous cell carcinoma (PSCC). However, the available biomarkers and detailed mechanisms underlying the metastasis of PSCC remain elusive. Here, we explored the expression landscape of HOX genes in twelve paired PSCC tissues, including primary tumors, metastatic lymph nodes and corresponding normal tissues, and highlighted that HOXD11 was indispensable in the progression of PSCC. HOXD11 was upregulated in PSCC cell lines and tumors, especially in metastatic lymph nodes. High HOXD11 expression was associated with aggressive features, such as advanced pN stages, extranodal extension, pelvic lymph node and distant metastasis, and predicted poor survival. Furthermore, tumorigenesis assays demonstrated that knockdown of HOXD11 not only inhibited the capability of cell proliferation, invasion and tumor growth but also reduced the burden of metastatic lymph nodes. Further mechanistic studies indicated that miR-138-5p was a tumor suppressor in PSCC by inhibiting the translation of HOXD11 post-transcriptionally through binding to the 3' untranslated region. Furthermore, HOXD11 activated the transcription of FN1 to decompose the extracellular matrix and to promote epithelial mesenchymal transition-like phenotype metastasis via FN1/MMP2/MMP9 pathways. Our study revealed that HOXD11 is a promising prognostic biomarker and predicts advanced disease with poor outcomes, which could serve as a potential therapeutic target for PSCC.

Indexed as

Carcinoma, Squamous CellMicroRNAsPenile Neoplasms3' Untranslated RegionsCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticGenes, HomeoboxHumansMaleMatrix Metalloproteinase 2Matrix Metalloproteinase 9Transcription Factors3' Untranslated RegionsMatrix Metalloproteinase 2Matrix Metalloproteinase 9MicroRNAsMIRN138 microRNA, humanMMP2 protein, humanMMP9 protein, humanTranscription Factors

Identifiers

PMID36151071
PMCPMC9508180
OpenAlexW4297036852

What Socratic 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 Socratic graph.