Evidence map›Paper›PMID 37243445›Full record

ReviewHuman gene therapy2023

Long Non-Coding RNAs, Cell Cycle, and Human Breast Cancer.

Qinan Yin, Haodi Ma, Gayan Bamunuarachchi, Xuewei Zheng, Yan Ma

Open access · greenAbstract readReview
In one paragraph

Review in Human gene therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 23 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

5 authors at 3 institutions in 2 countries.

Qinan YinPrecision Medicine Laboratory, College of Medical Technology and Engineering, Henan University of Science and Technology, Luoyang, China.ORCID 0000-0001-8560-5751
Haodi MaPrecision Medicine Laboratory, College of Medical Technology and Engineering, Henan University of Science and Technology, Luoyang, China.
Gayan BamunuarachchiDepartment of Medicine, Washington University School of Medicine in St. Louis, St. Louis, Missouri, USA.
Xuewei ZhengPrecision Medicine Laboratory, College of Medical Technology and Engineering, Henan University of Science and Technology, Luoyang, China.
Yan MaSpatial Navigation and Memory Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0003-3783-6795
Henan University of Science and Technology · CNNational Institute of Neurological Disorders and Stroke · USWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The long non-coding RNAs (lncRNAs) constitute an important class of the human transcriptome. The discovery of lncRNAs provided one of many unexpected results of the post-genomic era and uncovered a huge number of previously ignored transcriptional events. In recent years, lncRNAs are known to be linked with human diseases, with particular focus on cancer. Growing evidence has indicated that dysregulation of lncRNAs in breast cancer (BC) is strongly associated with the occurrence, development, and progress. Increasing numbers of lncRNAs have been found to interact with cell cycle progression and tumorigenesis in BC. The lncRNAs can exert their effect as a tumor suppressor or oncogene and regulate tumor development through direct or indirect regulation of cancer-related modulators and signaling pathways. What is more, lncRNAs are excellent candidates for promising therapeutic targets in BC due to the features of high tissue and cell-type specific expression. However, the underlying mechanisms of lncRNAs in BC still remain largely undefined. Here, we concisely summarize and sort out the current understanding of research progress in relationships of the roles for lncRNA in regulating the cell cycle. We also summarize the evidence for aberrant lncRNA expression in BC, and the potential for lncRNA to improve BC therapy is also discussed. Together, lncRNAs can be considered as exciting therapeutic candidates whose expression can be altered to impede BC progression.

Indexed as

Breast NeoplasmsRNA, Long NoncodingCell CycleFemaleHumansOncogenesTranscriptomeRNA, Long Noncodingbreast cancercell cyclelncRNAs

Identifiers

PMID37243445
PMCPMC10398747
OpenAlexW4378515394

What Socratic 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 Socratic graph.