Evidence map›Paper›PMID 38258348›Full record

ReviewAdvanced biology2024

Cellular and Exosomal MicroRNAs: Emerging Clinical Relevance as Targets for Breast Cancer Diagnosis and Prognosis.

Faith Mokobi Zablon, Parth Desai, Kristen Dellinger, Shyam Aravamudhan

Open access · hybridAbstract readReview
In one paragraph

Review in Advanced biology, 2024. 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
3.4field-weighted citation impact, top 7% 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, 12 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

4 authors at 2 institutions in 1 country.

Faith Mokobi ZablonDepartment of Nanoengineering, Joint School of Nanoscience and Nanoengineering, North Carolina, A&T State University, 2907 E. Gate City Blvd, Greensboro, NC, 27401, USA.ORCID 0000-0001-5391-5253
Parth DesaiDepartment of Nanoscience, Joint School of Nanoscience and Nanoengineering, University of North Carolina, 2904 E. Gate City Blvd, Greensboro, NC, 27401, USA.
Kristen DellingerDepartment of Nanoengineering, Joint School of Nanoscience and Nanoengineering, North Carolina, A&T State University, 2907 E. Gate City Blvd, Greensboro, NC, 27401, USA.ORCID 0000-0001-8193-7564
Shyam AravamudhanDepartment of Nanoengineering, Joint School of Nanoscience and Nanoengineering, North Carolina, A&T State University, 2907 E. Gate City Blvd, Greensboro, NC, 27401, USA.ORCID 0000-0001-9968-7188
North Carolina Agricultural and Technical State University · USUniversity of North Carolina at Greensboro · US

Funding

North Carolina Translational and Clinical Science Institute (NC TraCS) KL2KL2TR002490 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WEINBERGER, MORRIS · 2018 to 2022
$11.0M
A Diagnostic Platform for Extracellular Vesicle-Derived Biomarkers - Towards Early Detection of Alzheimer's DiseaseR16GM149496 · NIGMS · NORTH CAROLINA AGRI & TECH ST UNIV · PI Kristen Dellinger · 2023 to 2026
$563k
NCATS NIH HHS KL2 TR002490NIGMS NIH HHS R16 GM149496NIH HHS 1R16GM149496-01
6 · The paper itself

Abstract

Breast cancer accounts for the highest cancer cases globally, with 12% of occurrences progressing to metastatic breast cancer with a low survival rate and limited effective early intervention strategies augmented by late diagnosis. Moreover, a low concentration of prognostic and predictive markers hinders disease monitoring. Circulating and exosomal microRNAs (miRNAs) have recently shown a considerable interplay in breast cancer, standing out as effective diagnostic and prognostic markers. The primary functions are as gene regulatory agents at the genetic and epigenetic levels. An array of dysregulated miRNAs stimulates cancer-promoting mechanisms, activating oncogenes and controlling tumor-suppressing genes and mechanisms. Exosomes are vastly studied extracellular vesicles, carrying, and transporting cargo, including noncoding RNAs with premier roles in oncogenesis. Translocation of miRNAs from the circulation to exosomes, with RNA-binding proteins in stress-induced conditions, has shown significant cooperation in function to promote breast cancer. This review examines cellular and exosomal miRNA biogenesis and loading, the clinical implications of their dysregulation, their function in diagnosis, prognosis, and prediction of breast cancer, and in regulating cancer signaling pathways. The influence of cellular and exosomal miRNAs presents clinical significance on breast cancer diagnosis, subtyping, staging, prediction, and disease monitoring during treatment, hence a potent marker for breast cancer.

Indexed as

Breast NeoplasmsExosomesMicroRNAsClinical RelevanceFemaleHumansPrognosisMicroRNAsbiomarkerdiagnosisexosomal miRNAsexosomesmicroRNA (miRNA)prognosis

Identifiers

PMID38258348
PMCPMC11198028
OpenAlexW4391142610

What OpenQuestion holds

Textmetadata
LicenceTDM
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.