Evidence map›Paper›PMID 29844841›Full record

ArticleOncology letters2018

Expression of serum Hsa-miR-93 in uterine cancer and its clinical significance.

Shengquan Fang, Min Gao, Shilu Xiong, Qian Chen, Huifeng Zhang

Abstract read
In one paragraph

Article in Oncology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. MiRNA-93: a novel signature in human disorders and drug resistance.Cell communication and signaling : CCS · 2023
    Review
  2. Article
  3. 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

5 authors.

Shengquan FangDepartment of Gynecologic Oncology, Hubei Cancer Hospital, Wuhan, Hubei 430079, P.R. China.
Min GaoDepartment of Radiochemotherapy Oncology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China.
Shilu XiongDepartment of Gynecologic Oncology, Hubei Cancer Hospital, Wuhan, Hubei 430079, P.R. China.
Qian ChenDepartment of Gynecologic Oncology, Hubei Cancer Hospital, Wuhan, Hubei 430079, P.R. China.
Huifeng ZhangDepartment of Gynecologic Oncology, Hubei Cancer Hospital, Wuhan, Hubei 430079, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the study was to investigate the differential expression of micro-ribonucleic acid (miRNA)-93 in serum of patients with uterine cancer, and to explore the clinical significance. A total of 176 patients with uterine cancer who received surgery from May, 2009 to January, 2011 in the Department of Oncology of Hubei Cancer Hospital were selected. At the same time, 100 healthy individuals selected from the Physical Examination Center of Hubei Cancer Hospital comprised the control group. Mean age of patients was 55±11 years, and of the healthy individuals in the control group was 53±9 years. Blood was extracted from each participant to prepare serum samples. Change in the expression of serum miRNA-93 was detected by reverse transcription-polymerase chain reaction (RT-PCR), and the correlation between the expression of miRNA-93 and clinicopathological features of uterine cancer was analyzed. Expression level of miRNA-93 in serum of patients with uterine cancer was significantly lower than that in the healthy controls (P<0.05). Expression level of miRNA-93 was significantly correlated with pathological staging and lymph node metastasis (P<0.05). Receiver operating characteristic curve analysis showed that the area under curve was 0.781 and 95% confidence interval was 0.724-0.842. Survival rate of the high miRNA-93 expression group was significantly higher than that in the low miRNA-93 expression group (P=0.036). These results indicate that change in the expression of miRNA-93 is related to the occurrence of uterine cancer, and its decreased expression level suggests tumorigenesis.

Indexed as

micro-ribonucleic acid-93molecular markerpolymerase chain reactionreceiver operating characteristicuterine cancer

Identifiers

PMID29844841
PMCPMC5958810

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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.