Evidence map›Paper›PMID 25075250›Full record

ArticleAmerican journal of translational research2014

Epithelial and stromal expression of miRNAs during prostate cancer progression.

Qinghu Ren, Jiaqian Liang, Jianjun Wei, Olca Basturk, Jinhua Wang, Garrett Daniels, Lan Lin Gellert, Yirong Li, Ying Shen, Iman Osman and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. microRNAs and DICER1 are regulated by 1,25-dihydroxyvitamin D in prostate stroma.The Journal of steroid biochemistry and molecular biology · 2017
    Trial
  3. Review
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  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. MicroRNAs in prostate cancer: From function to biomarker discovery.Experimental biology and medicine (Maywood, N.J.) · 2018
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. A step-by-step microRNA guide to cancer development and metastasis.Cellular oncology (Dordrecht, Netherlands) · 2017
    Review
  20. Molecular mechanisms involving prostate cancer racial disparity.American journal of clinical and experimental urology · 2017
    Review
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 at 4 institutions in 3 countries.

Qinghu RenDepartment of Pathology, New York University School of Medicine New York, USA.
Jiaqian LiangDepartment of Pathology, New York University School of Medicine New York, USA ; Department of Urology, Wuhan No. 1 Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan, Hubei Province, China.
Jianjun WeiDepartment of Pathology, Northwestern University School of Medicine Chicago, IL, USA.
Olca BasturkDepartment of Pathology, New York University School of Medicine New York, USA.
Jinhua WangDepartment of NYU Cancer Institute, New York University School of Medicine New York, USA.
Garrett DanielsDepartment of Pathology, New York University School of Medicine New York, USA.
Lan Lin GellertDepartment of Pathology, New York University School of Medicine New York, USA.
Yirong LiDepartment of Pathology, New York University School of Medicine New York, USA.
Ying ShenDepartment of Pathology, New York University School of Medicine New York, USA.
Iman OsmanDepartment of Urology, New York University School of Medicine New York, USA.
Jun ZhaoDepartment of Urology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan, Hubei Province, China.
Jonathan MelamedDepartment of Pathology, New York University School of Medicine New York, USA.
Peng LeeDepartment of Pathology, New York University School of Medicine New York, USA ; Department of NYU Cancer Institute, New York University School of Medicine New York, USA ; Department of Urology, New York University School of Medicine New York, USA ; Department of New York Harbor Healthcare System, New York University School of Medicine New York, USA.
New York University · USHuazhong University of Science and Technology · CNNorthwestern University · USWuhan Union Hospital · CN

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
TRAINING PROGRAM IN MOLECULAR ONCOLOGY &IMMUNOLOGYT32CA009161 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CARROLL, WILLIAM L., LEVY, DAVID E · 1985 to 2020
$13.3M
Signaling Pathway Alterations in the Racial Disparity of Prostate CancerU01CA149556 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LEE, PENG, ZHANG, DAVID Y · 2011 to 2016
$1.9M
A signal pathway-based signature for metastatic prostate cancerI01BX001505 · VA · VA MEDICAL CENTER · PI LEE, PENG · 2014 to 2014
–
BLRD VA I01 BX001505NCI NIH HHS P30 CA016087NCI NIH HHS T32 CA009161NCI NIH HHS U01 CA149556
6 · The paper itself

Abstract

Global microRNA (miRNA) profile may predict prostate cancer (PCa) behaviors. In this study, we examined global miRNA expression by miRNA profiling as well as specific miRNA expression levels in PCa epithelium and stroma by in situ hybridization (ISH) and correlated with various clinicopathological features. We first performed comprehensive miRNA profiling on 27 macrodissected cases of PCa by miRNA microarray. A total of 299 miRNAs were significantly dysregulated in high grade and advanced stage PCa. We demonstrated that PCa can be readily classified into high grade/stage and low-grade/stage groups by its global miRNA expression profile. Next, we examined the expression of several selected dysregulated miRNAs, including let-7c, miR-21, miR-27a, miR-30c, and miR-219, in PCa by ISH. The levels of miRNA expression in epithelial and stromal cells were scored semiquantitatively and compared with clinicopathological features, including age, race, Gleason score, stage, PSA recurrence, metastasis, hormone resistance and survival. We found that the expression of miR-30c and miR-219 were significantly down-regulated in PCa. miR-21 and miR-30c were significantly down-regulated in PCa in African Americans compared to Caucasian Americans. In addition, down-regulation of let-7c, miR-21, miR-30c, and miR-219 are associated with metastatic disease. Furthermore, down-regulation of miR-30c and let-7c are significantly associated with androgen-dependent PCa. In PCa stromal cells, let-7c downregulation is significantly associated with extraprostatic extension. Our data suggest that selected miRNAs may serve as potential biomarkers to predict cancer progression.

Indexed as

miRNAprostate cancer progression

Identifiers

PMID25075250
PMCPMC4113495
OpenAlexW1913502161

What OpenQuestion holds

Textmetadata
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.