Evidence map›Paper›PMID 30852380›Full record

ArticleMolecular therapy. Nucleic acids2019

miR-582-3p and miR-582-5p Suppress Prostate Cancer Metastasis to Bone by Repressing TGF-β Signaling.

Shuai Huang, Changye Zou, Yubo Tang, Qingde Wa, Xinsheng Peng, Xiao Chen, Chunxiao Yang, Dong Ren, Yan Huang, Zhuangwen Liao and 3 more

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

67 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. The multifaceted roles of ribosomal P complex in cancer.World journal of surgical oncology · 2025
    Review
  6. Review
  7. Biomarkers in Localized Prostate Cancer: From Diagnosis to Treatment.International journal of molecular sciences · 2025
    Review
  8. Review
  9. Article
  10. Mechanistic studies ofFrontiers in oncology · 2025
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

7 more citing papers are in PubMed but not listed here.

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

13 authors.

Shuai HuangDepartment of Orthopaedic Surgery, The Second Affiliated Hospital of Guangzhou Medical University, 510260 Guangzhou, China; Department of Orthopaedic Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080 Guangzhou, China; Department of Guangdong Provincial Key Laboratory of Orthopaedics and Traumatology, 510080 Guangzhou, China. Electronic address: huang-shuai@hotmail.com.
Changye ZouDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080 Guangzhou, China; Department of Guangdong Provincial Key Laboratory of Orthopaedics and Traumatology, 510080 Guangzhou, China.
Yubo TangDepartment of Pharmacy, The First Affiliated Hospital of Sun Yat-sen University, 510080 Guangzhou, China.
Qingde WaDepartment of Orthopaedic Surgery, The Affiliated Hospital of Zunyi Medical College, 563003 Zunyi, China.
Xinsheng PengDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080 Guangzhou, China; Department of Guangdong Provincial Key Laboratory of Orthopaedics and Traumatology, 510080 Guangzhou, China.
Xiao ChenDepartment of Pharmacy, The First Affiliated Hospital of Sun Yat-sen University, 510080 Guangzhou, China.
Chunxiao YangDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Dong RenDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080 Guangzhou, China; Department of Guangdong Provincial Key Laboratory of Orthopaedics and Traumatology, 510080 Guangzhou, China.
Yan HuangDepartment of Orthopaedic Surgery, The Second Affiliated Hospital of Guangzhou Medical University, 510260 Guangzhou, China.
Zhuangwen LiaoDepartment of Orthopaedic Surgery, The Second Affiliated Hospital of Guangzhou Medical University, 510260 Guangzhou, China.
Sheng HuangDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Nanchang University, 330006 Nanchang, China.
Xuenong ZouDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080 Guangzhou, China; Department of Guangdong Provincial Key Laboratory of Orthopaedics and Traumatology, 510080 Guangzhou, China. Electronic address: zxnong@hotmail.com.
Jincheng PanDepartment of Urology Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080 Guangzhou, China. Electronic address: panjinchengos@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A number of studies have reported that aberrant expression of microRNAs (miRNAs) closely correlates with the bone metastasis of prostate cancer (PCa). However, clinical significance and functional roles of both strands of a single miRNA in bone metastasis of PCa remain undefined. Here, we reported that miR-582-3p and miR-582-5p expression were simultaneously reduced in bone metastatic PCa tissues compared with non-bone metastatic PCa tissues. Downexpression of miR-582-3p and miR-582-5p strongly and positively correlated with advanced clinicopathological characteristics and shorter bone metastasis-free survival in PCa patients. Upregulating miR-582-3p and miR-582-5p inhibited invasion and migration abilities of PCa cells in vitro, as well as repressed bone metastasis in vivo. Our results further revealed that miR-582-3p and miR-582-5p attenuated bone metastasis of PCa via inhibiting transforming growth factor β (TGF-β) signaling by simultaneously targeting several components of TGF-β signaling, including SMAD2, SMAD4, TGF-β receptor I (TGFBRI), and TGFBRII. Moreover, deletion contributes to miR-582-3p and miR-582-5p downexpression in PCa tissues. Finally, clinical negative correlations of miR-582-3p and miR-582-5p with SMAD2, SMAD4, TGFBRI, and TGFBRII were demonstrated in PCa tissues. Thus, our findings explore a novel tumor-suppressive miRNA with its both strands implicated in bone metastasis of PCa, suggesting its potential therapeutic value in treatment of PCa bone metastasis.

Identifiers

PMID30852380
PMCPMC6409413

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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.