Evidence map›Paper›PMID 38139352›Full record

ReviewInternational journal of molecular sciences2023

Functional and Potential Therapeutic Implication of MicroRNAs in Pancreatic Cancer.

Amartya Pal, Anushka Ojha, Jingfang Ju

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

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

13 citing papers in PubMed.

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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

3 authors.

Amartya PalDepartment of Pathology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY 11794, USA.ORCID 0009-0006-7546-942X
Anushka OjhaDepartment of Pathology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY 11794, USA.ORCID 0009-0008-7220-4201
Jingfang JuDepartment of Pathology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY 11794, USA.

Funding

BLRD VA I01 BX005260NCI NIH HHS R01CA1550197098
6 · The paper itself

Abstract

The alarmingly low five-year survival rate for pancreatic cancer presents a global health challenge, contributing to about 7% of all cancer-related deaths. Late-stage diagnosis and high heterogeneity are the biggest hurdles in treating pancreatic cancer. Thus, there is a pressing need to discover novel biomarkers that could help in early detection as well as improve therapeutic strategies. MicroRNAs (miRNAs), a class of short non-coding RNA, have emerged as promising candidates with regard to both diagnostics and therapeutics. Dysregulated miRNAs play pivotal roles in accelerating tumor growth and metastasis, orchestrating tumor microenvironment, and conferring chemoresistance in pancreatic cancer. The differential expression profiles of miRNAs in pancreatic cancer could be utilized to explore novel therapeutic strategies. In this review, we also covered studies on recent advancements in various miRNA-based therapeutics such as restoring miRNAs with a tumor-suppressive function, suppressing miRNA with an oncogenic function, and combination with chemotherapeutic drugs. Despite several challenges in terms of specificity and targeted delivery, miRNA-based therapies hold the potential to revolutionize the treatment of pancreatic cancer by simultaneously targeting multiple signaling pathways.

Indexed as

MicroRNAsPancreatic NeoplasmsBiomarkers, TumorGene Expression Regulation, NeoplasticHumansSignal TransductionTumor MicroenvironmentBiomarkers, TumorMicroRNAsbiomarkermiRNApancreatic cancerresistancetherapeutics

Identifiers

PMID38139352
PMCPMC10744132

What Socratic holds

Textmetadata
LicenceCC BY
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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.