Evidence map›Paper›PMID 36416311›Full record

ReviewInternational journal of molecular medicine2023

Exosomal delivery of TRAIL and miR‑335 for the treatment of hepatocellular carcinoma (Review).

Nikita Thapa, Yong Joon Chwae, Kwang Ho Yoo, Tae-Bin Won, Daewook Kang, Daae Choi, Jaeyoung Kim

Abstract readReview
In one paragraph

Review in International journal of molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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, 1 synthesis or guideline pooled it.

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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.

Nikita Thapa *CK‑Exogene, Inc., Seongnam, Gyeonggi‑do 13201, Republic of Korea.
Yong Joon Chwae *Department of Microbiology, Ajou University School of Medicine, Suwon, Gyeonggi‑do 16499, Republic of Korea.
Kwang Ho Yoo *Department of Dermatology, Chung‑Ang University College of Medicine, Seoul 06973, Republic of Korea.
Tae-Bin WonDepartment of Otorhinolaryngology, Seoul National University Hospital, Seoul 03080, Republic of Korea.
Daewook KangDepartment of Microbiology, Ajou University School of Medicine, Suwon, Gyeonggi‑do 16499, Republic of Korea.
Daae ChoiDepartment of Microbiology, Ajou University School of Medicine, Suwon, Gyeonggi‑do 16499, Republic of Korea.
Jaeyoung KimCK‑Exogene, Inc., Seongnam, Gyeonggi‑do 13201, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver cancer is the sixth most prevalent type of cancer worldwide and accounts for the third most frequent cause of cancer‑associated mortality. Conventional anticancer drugs display limited efficacy owing to their short half‑life, poor solubility and inefficient drug delivery. Despite advancements being made in drug discovery and development for the treatment of hepatocellular carcinoma (HCC), drug inefficacy and drug continue to pose significant obstacles to effective treatment. Therefore, it is imperative that novel treatment strategies be developed with the aim of developing anticancer treatments without any side‑effects and with long‑term durability. Extracellular vesicles, such as exosomes, intercellular communication agents which have the ability to carry heterogenous molecules with high penetrability, low immunogenicity and longer durability, may provide a versatile natural delivery system. The present review article illustrates the innovative treatment strategy using exosomes as a delivery agent for two distinct anticancer candidates, i.e., tumor necrosis factor‑related apoptosis‑inducing ligand and microRNA‑335. The aim of the present review was to present a unique strategy for the development of an exceptional anticancer treatment therapy exploiting exosomes as a delivery vehicle which may be used for HCC.

Indexed as

Carcinoma, HepatocellularExosomesLiver NeoplasmsMicroRNAsHumansTNF-Related Apoptosis-Inducing LigandMicroRNAsMIRN335 microRNA, humanTNF-Related Apoptosis-Inducing Ligandanticancer therapydrug resistanceexosomeshepatocellular carcinomamiR335tumor necrosis factor‑related apoptosis‑inducing ligand

Identifiers

PMID36416311
PMCPMC9728509

What OpenQuestion holds

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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 OpenQuestion graph.