Evidence map›Paper›PMID 33613846›Full record

ArticleOncotarget2021

MicroRNA-214 enriched exosomes from human cerebral endothelial cells (hCEC) sensitize hepatocellular carcinoma to anti-cancer drugs.

Louie Semaan, Qingning Zeng, Yong Lu, Yi Zhang, Mehdi Mohamad Zreik, Mohamad Baqer Chamseddine, Michael Chopp, Zheng Gang Zhang, Dilip Moonka

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  13. Exosomes as potential diagnosis and treatment for liver cancer.World journal of gastrointestinal oncology · 2022
    Article
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  15. Microvesicles: the functional mediators in sorafenib resistance.Cancer drug resistance (Alhambra, Calif.) · 2022
    Review
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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

9 authors at 3 institutions in 1 country.

Louie SemaanDepartment of Neurology, Henry Ford Hospital, Detroit, MI 48202, USA.
Qingning ZengDepartment of Neurology, Henry Ford Hospital, Detroit, MI 48202, USA.
Yong LuDepartment of Neurology, Henry Ford Hospital, Detroit, MI 48202, USA.
Yi ZhangDepartment of Neurology, Henry Ford Hospital, Detroit, MI 48202, USA.
Mehdi Mohamad ZreikDepartment of Neurology, Henry Ford Hospital, Detroit, MI 48202, USA.
Mohamad Baqer ChamseddineDepartment of Neurology, Henry Ford Hospital, Detroit, MI 48202, USA.
Michael ChoppDepartment of Neurology, Henry Ford Hospital, Detroit, MI 48202, USA.
Zheng Gang ZhangDepartment of Neurology, Henry Ford Hospital, Detroit, MI 48202, USA.
Dilip MoonkaDivision of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, MI 48202, USA.
Henry Ford Hospital · USUniversity of Michigan–Dearborn · USWayne State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common primary liver tumor worldwide. Current medical therapy for HCC has limited efficacy. The present study tests the hypothesis that human cerebral endothelial cell-derived exosomes carrying elevated miR-214 (hCEC-Exo-214) can amplify the efficacy of anti-cancer drugs on HCC cells. Treatment of HepG2 and Hep3B cells with hCEC-Exo-214 in combination with anti-cancer agents, oxaliplatin or sorafenib, significantly reduced cancer cell viability and invasion compared with monotherapy with either drug. Additionally, the therapeutic effect of the combination therapy was detected in primary tumor cells derived from patients with HCC. The ability of hCEC-Exo-214 in sensitizing HCC cells to anti-cancer drugs was specific, in that combination therapy did not affect the viability and invasion of human liver epithelial cells and non-cancer primary cells. Furthermore, compared to monotherapy with oxaliplatin and sorafenib, hCEC-Exo-214 in combination with either drug substantially reduced protein levels of P-glycoprotein (P-gp) and splicing factor 3B subunit 3 (SF3B3) in HCC cells. P-gp and SF3B3 are among miR-214 target genes and are known to mediate drug resistance and cancer cell proliferation, respectively. In conclusion, the present

Indexed as

anti-cancer drughepatocellular carcinoma (HCC)human cerebral endothelial cells-derived exosomesmicroRNA-214therapeutic efficacy

Identifiers

PMID33613846
PMCPMC7869574
OpenAlexW3128629953

What Socratic holds

Textmetadata
LicenceCC BY
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.