Melanoma cell line-derived exosomal miR-424-5p: a key promoter of angiogenesis through LATS2 interaction

Melanoma cell-derived exosomal miR-424-5p promotes angiogenesis by targeting LATS2, contributing to melanoma progression. Targeting the exosomal miR-424-5p/LATS2 axis could be a potential therapeutic strategy for melanoma.

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Publication Details

Journal
Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics
Published
2024-08-26
DOI
https://doi.org/10.32604/or.2024.050878
Citations
4
Primary Topic
Cell Adhesion Molecules Research
Type
article
Field-Weighted Citation Impact
1.53
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article

Melanoma cell line-derived exosomal miR-424-5p: a key promoter of angiogenesis through LATS2 interaction

Renbing Jiang, Maierdanjiang Maihemuti, Zhang Qiang, Haiyang He et al.
4 citations
Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics
Cell Adhesion Molecules Research
1.53
article

Melanoma cell line-derived exosomal miR-424-5p: a key promoter of angiogenesis through LATS2 interaction

Renbing Jiang, Maierdanjiang Maihemuti, Zhang Qiang, Haiyang He, Junwei DU, Jing Zhang
article en
4 citations

Abstract

Melanoma cell-derived exosomal miR-424-5p promotes angiogenesis by targeting LATS2, contributing to melanoma progression. Targeting the exosomal miR-424-5p/LATS2 axis could be a potential therapeutic strategy for melanoma.

Oncology Research Featuring Preclinical and Clinical Cancer TherapeuticsVol. 33(2)
Xinjiang Medical University (CN), Tumor Hospital of Xinjiang Medical University (CN)
Zero hunger
Openalex Percentile: Top 17%
Cell Adhesion Molecules Research
1.53
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