Evidence map›Paper›PMID 36466338›Full record

ReviewFrontiers in bioengineering and biotechnology2022

Exploiting the potential of extracellular vesicles as delivery vehicles for the treatment of melanoma.

Chongchao Hou, Qiang Wu, Lizhou Xu, Rongwei Cui, Rongying Ou, Danyang Li, Yunsheng Xu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in bioengineering and biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Editorial: The functions of extracellular vesicles in melanoma.Frontiers in cell and developmental biology · 2023
    Article
  7. Review
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.

Chongchao HouThe Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Qiang WuThe Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Lizhou XuZJU-Hangzhou Global Scientific and Technological Innovation Center, Hangzhou, China.
Rongwei CuiThe Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Rongying OuDepartment of Gynaecology and Obstetrics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Danyang LiThe Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Yunsheng XuThe Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
The Seventh Affiliated Hospital of Sun Yat-sen University · CNFirst Affiliated Hospital of Wenzhou Medical University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma, the most aggressive skin cancer that originated from genetic mutations in the melanocytes, is still a troublesome medical problem under the current therapeutic approaches, which include surgical resection, chemotherapy, photodynamic therapy, immunotherapy, biochemotherapy and targeted therapy. Nanotechnology has significantly contributed to the development of cancer treatment in the past few years, among which extracellular vesicles (EVs) are nanosized lipid bilayer vesicles secreted from almost all cells that play essential roles in many physiological and pathological processes. In terms of melanoma therapy, the unique physicochemical properties of EVs make them promising nanocarriers for drug transportation compared to other synthetic nanocarriers. Moreover, EVs can be further engineered to maximize their drug delivery potential. Herein, in this minireview, we gave a brief overview of EV-based drug delivery strategies for melanoma therapy, in which different therapeutics delivered

Indexed as

chemotherapydrug deliveryendogenous miRNAsextracellular vesicleimmunotherapymelanomaphotothermal therapy (PPT)radiotherapy

Identifiers

PMID36466338
PMCPMC9714302
OpenAlexW4309269231

What OpenQuestion 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 OpenQuestion graph.