Evidence map›Paper›PMID 34599680›Full record

ArticleCancer chemotherapy and pharmacology2021

EVs delivery of miR-1915-3p improves the chemotherapeutic efficacy of oxaliplatin in colorectal cancer.

Zhenhuan Xiao, Yun Liu, Qun Li, Qinyuan Liu, Yong Liu, Yan Luo, Songzhi Wei

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer chemotherapy and pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

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  9. Targeting the deubiquitinaseOncology reports · 2023
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  16. The value of exosome-derived noncoding RNAs in colorectal cancer proliferation, metastasis, and clinical applications.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  17. The Role of Exosomal Non-Coding RNAs in Colorectal Cancer Drug Resistance.International journal of molecular sciences · 2022
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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 3 institutions in 1 country.

Zhenhuan XiaoDepartment of General Surgery, The Shenzhen Hospital of Southern Medical University, Shenzhen, China.
Yun LiuDepartment of Pediatrics, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Qun LiHealth Management Center, The Shenzhen Hospital of Southern Medical University, Shenzhen, China.
Qinyuan LiuDepartment of General Surgery, The Shenzhen Hospital of Southern Medical University, Shenzhen, China.
Yong LiuDepartment of Oncology, The People's Hospital of Leping City, Jingdezhen, China.
Yan LuoDepartment of Oncology, The Third Affiliated Hospital of Nanchang University, Nanchang, China.
Songzhi WeiDepartment of Oncology, The Third Hospital of Nanchang, No. 2 Xiangshannan Road, Nanchang, China. wstwsz@127.com.ORCID 0000-0003-3562-0288
Nanchang University · CNSouthern Medical University Shenzhen Hospital · CNThird Hospital of Nanchang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOxaliplatin is a crucial component of the combinatorial chemotherapeutic standard of care for advanced colorectal cancer (CRC). Unfortunately, a serious barrier to effective oxaliplatin treatment is drug resistance due to epithelial-mesenchymal transitioning (EMT). Interestingly, stable oxaliplatin-resistant CRC cell lines show differential expression of miR-1915-3p; thus, this microRNA may represent a potential modifier of oxaliplatin resistance in CRC cells.

methodsmiR-1915-3p was over-expressed in oxaliplatin-resistant CRC cells and a non-tumorigenic intestinal cell line (FHC) via lentiviral transduction. Extracellular vesicles (EVs) were purified from transduced FHC cells and co-incubated with CRC cells. Expression levels of miR-1915-3p and other RNA species were assessed by RT-qPCR, while protein expression levels were assessed by Western blotting. The effects of miR-1915-3p on CRC viability were evaluated by proliferation, apoptosis assays, and Transwell assays. Effects of miR-1915-3p over-expression on in vivo oxaliplatin sensitivity was tested via murine xenograft models.

resultsmiRNA-1915-3p decreased EMT marker expression in oxaliplatin-resistant CRC cell lines and in vivo. FHC cells were able to produce and secrete miR-1915-3p-containing EVs, which we employed to mediate miR-1915-3p delivery to oxaliplatin-resistant CRC cells and increase their oxaliplatin sensitivity in vivo and in vitro. Mechanistically, miR-1915-3p overexpression downregulated the EMT-promoting oncogenes 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (PFKFB3) and ubiquitin carboxyl-terminal hydrolase 2 (USP2) as well as upregulated E-cadherin (a cell adhesion mediator). miR-1915-3p's effects on chemosensitivity and EMT were mediated by its regulation of PFKFB3 and USP2.

conclusionExosomal delivery of miR-1915-3p can improve the chemotherapeutic efficacy of oxaliplatin in CRC cells by suppressing the EMT-promoting oncogenes PFKFB3 and USP2.

Indexed as

Drug Resistance, NeoplasmAnimalsAntineoplastic AgentsApoptosisCell ProliferationColorectal NeoplasmsExosomesHumansMiceMicroRNAsOxaliplatinTumor Cells, CulturedXenograft Model Antitumor AssaysAntineoplastic AgentsMicroRNAsMIRN1915 microRNA, humanOxaliplatinChemoresistanceChemosensitivityColorectal cancermiR-1915-3pOxaliplatin

Identifiers

PMID34599680
OpenAlexW3203405581

What OpenQuestion 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 OpenQuestion graph.