Evidence map›Paper›PMID 31938391›Full record

ArticleInternational journal of clinical and experimental pathology2018

Serum miR-342-3p is a novel diagnostic and prognostic biomarker for non-small cell lung cancer.

Yingzhi Qin, Xiaoyun Zhou, Cheng Huang, Li Li, Hongsheng Liu, Naixin Liang, Yeye Chen, Dongjie Ma, Zhijun Han, Xiaohui Xu and 2 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Yingzhi QinDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Xiaoyun ZhouDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Cheng HuangDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Li LiDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Hongsheng LiuDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Naixin LiangDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Yeye ChenDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Dongjie MaDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Zhijun HanDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Xiaohui XuDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Jia HeDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Shanqing LiDepartment of Thoracic Surgery, Peking Union Medical College Hospital (PUMCH) Beijing 100730, China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the leading cause of cancer-related mortality and non-small cell lung carcinoma (NSCLC) is the most common type. MicroRNAs (miRNAs) are small non-coding RNAs that negatively regulate gene expression at the post-transcriptional level. Aberrant expression of miRNAs has been demonstrated to be a prominent feature in NSCLC. The aim of this study was to determine the potential clinical value of serum miR-342-3p in NSCLC. We first evaluated the miR-342-3p levels in NSCLC cell lines, culture media of NSCLC cell lines, and serum samples from NSCLC patients as well as in their respective controls. The associations between serum miR-342-3p levels and clinicopathological parameters as well as clinical outcome were then determined. miR-342-3p expression was significantly downregulated in NSCLC cell lines, culture media of NSCLC cell lines, and the serum samples from NSCLC patients compared to their controls. Serum miR-342-3p discriminated NSCLC patients from healthy individuals. Low expression of serum miR-342-3p was significantly associated with advanced TNM stage and positive lymph node metastasis. In addition, NSCLC patients in the low serum miR-342-3p expression group had remarkably shorter overall survival than those in the high serum miR-342-3p expression group. Serum miR-342-3p was shown to be an independent prognosis factor. In conclusion, serum miR-342-3p might be a promising biomarker for NSCLC that can be used to improve diagnosis and prognosis.

Indexed as

biomarkerdiagnosisNon-small cell lung carcinomaprognosisserum miR-342-3p

Identifiers

PMID31938391
PMCPMC6958259
OpenAlexW3028058445

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.