Evidence map›Paper›PMID 26339409›Full record

ArticleInternational journal of clinical and experimental pathology2015

Prognostic implications of tissue and serum levels of microRNA-128 in human prostate cancer.

Xiaoke Sun, Zhen Yang, Yu Zhang, Jing He, Feng Wang, Pengxiao Su, Juanli Han, Zhe Song, Yanjiang Fei

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. MicroRNA-128 acts as a suppressor in the progression of gastrointestinal stromal tumor by targeting B-lymphoma Mo-MLV insertion region 1.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

9 authors.

Xiaoke SunDepartment of Surgery, Xi'an Honghui Hospital Xi'an 710054, China.
Zhen YangDepartment of Surgery, Xi'an Honghui Hospital Xi'an 710054, China.
Yu ZhangDepartment of Infectious Diseases, Children's Hospital of Xi'an Xi'an 710003, China.
Jing HeDepartment of Surgery, Xi'an Honghui Hospital Xi'an 710054, China.
Feng WangDepartment of Surgery, Xi'an Honghui Hospital Xi'an 710054, China.
Pengxiao SuDepartment of Surgery, Xi'an Honghui Hospital Xi'an 710054, China.
Juanli HanDepartment of Surgery, Xi'an Honghui Hospital Xi'an 710054, China.
Zhe SongDepartment of Surgery, Xi'an Honghui Hospital Xi'an 710054, China.
Yanjiang FeiDepartment of Surgery, Xi'an Honghui Hospital Xi'an 710054, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeMicroRNA-128 (miR-128) has been identified as a negative regulator of malignant phenotypes of prostate cancer (PCa) cells. The aim of this study was to evaluate the prognostic implications of both tissue and serum levels of miR-128 expression in PCa patients undergoing radical prostatectomy.

methodsA series of 128 cases with PCa were evaluated for both tissue and serum levels of miR-128 expression by quantitative reverse-transcription PCR.

resultsCompared with non-cancerous prostate tissues and normal sera, both tissue and serum levels of miR-128 expression were significantly decreased in PCa patients (both P<0.001). Importantly, there was a close correlation between tissue and serum levels of miR-128 expression in PCa patients (rs=0.808, P<0.001). Then, low miR-128 expression in both PCa tissues and patients' sera were dramatically associated with aggressive clinicopathological features, including advanced pathological stage (both P=0.001), positive lymph node metastasis (P=0.006 and 0.01, respectively), high preoperative PSA (both P=0.01) and positive angiolymphatic invasion (both P=0.02). Moreover, Kaplan-Meier survival analysis showed that low miR-128 expression in both PCa tissues and patients' sera were significantly associated with short biochemical recurrence (BCR)-free survival. Furthermore, multivariate analysis indicated that both tissue and serum levels of miR-128 expression were independent prognostic factors for BCR-free survival of PCa patients.

conclusionOur data suggest that the decreased expression of miR-128 in both tissue and serum samples of PCa patients may be associated with tumor malignant progression and BCR-free survival. Particularly, serum miR-128 may be developed as a novel noninvasive biomarker for PCa diagnosis and prognosis.

Indexed as

AgedBiomarkers, TumorChi-Square DistributionDisease-Free SurvivalDisease ProgressionDown-RegulationGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateLymphatic MetastasisMaleMicroRNAsMultivariate AnalysisNeoplasm StagingPredictive Value of TestsProportional Hazards ModelsBiomarkers, TumorMicroRNAsMIRN128 microRNA, humanclinical pathologymicroRNA-128prognosisProstate cancerserum

Identifiers

PMID26339409
PMCPMC4555737

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.