Evidence map›Paper›PMID 32869851›Full record

SynthesisBioscience reports2020

Meta-analysis of the clinicopathological significance of miRNA-145 in breast cancer.

Peng Lv, Zhenzhu Zhang, Li Hou, Yayue Zhang, Lingeng Lu, Chong Wang, Fengqin Shi

Abstract readMeta-Analysis
In one paragraph

Synthesis in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

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

  1. Pooled it
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  5. Non-Coding RNAs in Breast Cancer: Diagnostic and Therapeutic Implications.International journal of molecular sciences · 2024
    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

7 authors.

Peng LvDepartment of Oncology and Hematology, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, 5 Haiyuncang Street, Dongcheng District, Beijing 100700, China.
Zhenzhu ZhangDepartment of Oncology and Hematology, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, 5 Haiyuncang Street, Dongcheng District, Beijing 100700, China.
Li HouDepartment of Oncology and Hematology, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, 5 Haiyuncang Street, Dongcheng District, Beijing 100700, China.
Yayue ZhangDepartment of Oncology and Hematology, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, 5 Haiyuncang Street, Dongcheng District, Beijing 100700, China.
Lingeng LuDepartment of Chronic Disease Epidemiology, Yale School of Public Health, School of Medicine, Yale University, New Haven, CT 06520, U.S.A.
Chong WangDepartment of Oncology and Hematology, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, 5 Haiyuncang Street, Dongcheng District, Beijing 100700, China.
Fengqin ShiDepartment of Oncology and Hematology, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, 5 Haiyuncang Street, Dongcheng District, Beijing 100700, China.

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

Low expression of tumor suppressor microRNA (miRNA) and high expression of carcinogenic miRNA promote the occurrence and progression of human cancer. Most studies show that miR-145 is a tumor suppressor miRNA, and is closely related to the clinicopathology of breast cancer. However, the results are still inconsistent. Therefore, we conducted a meta-analysis on the basis of eligible studies to summarize the possible correlation between miR-145 and the clinicopathology and prognosis of breast cancer. Using PubMed, Embase, Web of Science, Wanfang and CNKI, we searched all published papers written in either English or Chinese on miR-145 expression in breast cancer from 1990 to November 2019 for meta-analysis. We used standardized mean difference (SMD) to evaluate the differential expression of miR-145 in breast cancer tissues and adjacent normal tissues or normal breast tissues. We found that miR-145 expression was significantly lower in breast cancer tissues than that in adjacent normal tissues (SMD = -2.93, P<0.0001) and in healthy women (SMD = -0.52, P=0.009). miR-145 expression was lower in breast cancer patients with ER-positive (SMD = 0.65, P<0.001), HER-2-positive (SMD = -1.04, P<0.001), compared with their counterparts, respectively. In addition, breast cancer patients with low expression of miR-145 had larger tumor diameters (SMD = -1.97, P<0.001) and lymph node metastasis (SMD = -1.75, P<0.001) that are unfavorable prognostic factors. Conclusion: Low miR-145 is observed in breast cancer, which is closely related to molecular subtypes and unfavorable factors of breast cancer. These findings indicate that miR-145 is tumor suppressor miRNA, and may be a potential diagnostic and prognostic marker in breast cancer.

Indexed as

Gene Expression Regulation, NeoplasticBiomarkers, TumorBreastBreast NeoplasmsFemaleHumansLymphatic MetastasisMicroRNAsTumor BurdenBiomarkers, TumorMicroRNAsMIRN145 microRNA, humanbreast carcinomameta- analysisMicroRNAmiR-145

Identifiers

PMID32869851
PMCPMC7502658

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Registered trials

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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.