Evidence map›Paper›PMID 38329638›Full record

ArticleMolecular biology reports2024

Horizontal transfer of miR-383 sensitise cells to cisplatin by targeting VEGFA-Akt signalling loop.

Grace R Raji, Aswini Poyyakkara, T V Sruthi, Lincy Edatt, K Haritha, S Sharath Shankar, V B Sameer Kumar

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 98% 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

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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

2 citing papers in PubMed, 0 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

7 authors at 4 institutions in 2 countries.

Grace R RajiDepartment of Biochemistry and Molecular Biology, School of Biological Sciences, Central University of Kerala, Kasaragod, Kerala, 671316, India.
Aswini PoyyakkaraDepartment of Biochemistry and Molecular Biology, School of Biological Sciences, Central University of Kerala, Kasaragod, Kerala, 671316, India.
T V SruthiDepartment of Medicine, Thomas Jefferson University, Jefferson Alumni Hall, 1020 Locust Street, Philadelphia, PA, 19107, USA.
Lincy EdattLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27516, USA.
K HarithaDepartment of Pediatrics, Neurooncology Division and Aflac Cancer and Blood Disorders Centre of Childrens Healthcare of Atlanta, Emory University, Atlanta, GA, 30322, USA.
S Sharath ShankarDepartment of Medicine, Thomas Jefferson University, Jefferson Alumni Hall, 1020 Locust Street, Philadelphia, PA, 19107, USA.
V B Sameer KumarDepartment of Genomic Science, School of Biological Sciences, Central University of Kerala, Kasaragod, Kerala, 671316, India. sameerkumarvb@gmail.com.ORCID http://orcid.org/0000-0002-0895-0241
Central University of Kerala · INThomas Jefferson University · USEmory University · USUniversity of North Carolina at Chapel Hill · US

Funding

Kerala Biotechnology Commission 023/YIPB/KBC/2013/KSCSTE
6 · The paper itself

Abstract

backgroundCellular resistance to cisplatin has been one of the major obstacles in the success of combination therapy for many types of cancers. Emerging evidences suggest that exosomes released by drug resistant tumour cells play significant role in conferring resistance to drug sensitive cells by means of horizontal transfer of genetic materials such as miRNAs. Though exosomal miRNAs have been reported to confer drug resistance, the exact underlying mechanisms are still unclear. METHODS AND

resultsIn the present study, mature miRNAs secreted differentially by cisplatin resistant and cisplatin sensitive HepG2 cells were profiled and the effect of most significantly lowered miRNA in conferring cisplatin resistance when horizontally transferred, was analysed. we report miR-383 to be present at the lowest levels among the differentially abundant miRNAs expressed in exosomes secreted by cisplatin resistant cells compared to that that of cisplatin sensitive cells. We therefore, checked the effect of ectopic expression of miR-383 in altering cisplatin sensitivity of Hela cells. Drug sensitivity assay and apoptotic assays revealed that miR-383 could sensitise cells to cisplatin by targeting VEGF and its downstream Akt mediated pathway.

conclusionResults presented here provide evidence for the important role of miR-383 in regulating cisplatin sensitivity by modulating VEGF signalling loop upon horizontal transfer across different cell types.

Indexed as

CisplatinMicroRNAsHeLa CellsHumansProto-Oncogene Proteins c-aktVascular Endothelial Growth Factor ACisplatinMicroRNAsMIRN383 microRNA, humanProto-Oncogene Proteins c-aktVascular Endothelial Growth Factor AVEGFA protein, humanAktCisplatin resistanceExosomesmiR-383VEGF

Identifiers

PMID38329638
OpenAlexW4391651729

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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.