Evidence map›Paper›PMID 39342305›Full record

ArticleCancer cell international2024

M1 macrophage-derived exosomal microRNA-29c-3p suppresses aggressiveness of melanoma cells via ENPP2.

Byoungha An, Cheol-Hee Shin, Jae Won Kwon, Na Ly Tran, A Hui Kim, Hyeyeon Jeong, Sang-Heon Kim, Kwideok Park, Seung Ja Oh

Abstract read
In one paragraph

Article in Cancer cell international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–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

14 citing papers in PubMed.

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  12. Multi-omics elucidation ofFrontiers in nutrition · 2025
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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.

Byoungha AnCenter for Biomaterials, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Cheol-Hee ShinCenter for Biomaterials, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Jae Won KwonCenter for Biomaterials, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Na Ly TranDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si, Gyeonggi-do, 17104, Republic of Korea.
A Hui KimDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si, Gyeonggi-do, 17104, Republic of Korea.
Hyeyeon JeongDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si, Gyeonggi-do, 17104, Republic of Korea.
Sang-Heon KimCenter for Biomaterials, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Kwideok ParkCenter for Biomaterials, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Seung Ja OhDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si, Gyeonggi-do, 17104, Republic of Korea. seungja.oh@khu.ac.kr.

Funding

by National Research Foundation (NRF) grant funded by the Korea government RS-2023-00208795Kyung Hee University KHU-20222227National Research Foundation (NRF) grant funded by the Korea government RS-2023-00260529
6 · The paper itself

Abstract

In the tumor microenvironment, macrophages play crucial roles resulting in tumor suppression and progression, depending on M1 and M2 macrophages, respectively. In particular, macrophage-derived exosomes modulate the gene expression of cancer cells by delivering miRNAs which downregulate specific genes. The communication between macrophages and cancer cells is especially important in immunogenic tumors such as melanoma, where the cancer pogression is significantly influenced by the surrounding immune cells. In this study, we identified that M1 macrophages secrete exosomal miR-29c-3p in the co-culture system with melanoma cells. Simultaneously, ENPP2, the target of miR-29c-3p, decreased in the melanoma cells which are co-cultured with M1 macrophages. Additionally, we observed that the reduction of ENPP2 alleviates melanoma cell migration and invasion, due to the changes of cholesterol metabolism and ECM remodeling. Based on these findings, we demonstrated that M1 macrophages suppress aggressiveness of melanoma cells via exosomal miR-29c-3p-mediated knock-down of ENPP2 in cancer cells.

Indexed as

ENPP2Exosomal miR-29c-3pM1 macrophageMelanomaTumor microenvironment

Identifiers

PMID39342305
PMCPMC11438108

What Socratic holds

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Registered trials

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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 Socratic graph.