Virus-mimetic nanovesicle for the Hijacking- Integration-Vesicular amplification-Exocytosis treatment of ocular tumor

We developed a kind of virus-mimetic nanovesicle (Mel-VSVG-NA), which could react with tumor cells in a membrane fusion procedure (named as First Fusion ), result by the function of Vesicular Stomatitis Virus Glycoprotein (VSVG) in acid microenvironment. Meanwhile, the melittin on Mel-VSVG-NA was transfer on the surface of targeted tumor cell, and thus execute hole-digging process on the tumor cell membrane, causing severe cell content loss and suppression of tumor growth. After the first-round treatment, a harmless ultrasound exposure was carried out, the further engineered vesicles were generated from the damaged cells. Afterwards, the produced vesicles were also confirmed to engineered with VSVG and melittin, which could further fuse with other tumor cells and induced another cell death (named as Second Fusion ). These results indicated that Mel-VSVG-NA is a reliable advance of nano-treatment in ocular tumor therapy, and we bring in this concept of Hijacking- Integration-Vesicular amplification-Exocytosis mode as HIVE therapy. • A Hijacking- Integration-Vesicular amplification-Exocytosis treatment was constructed. • The Mel-VSVG-NA could induce a fusion procedure and execute the hole-digging process, thus induce the cellular damage. • The Mel-VSVG-NA treated MUM-2B cells could in situ produce nanovesicle by an ultrasound stimulation.

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Publication Details

Journal
Materials Today Advances
Published
2025-10-31
DOI
https://doi.org/10.1016/j.mtadv.2025.100643
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
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article

Virus-mimetic nanovesicle for the Hijacking- Integration-Vesicular amplification-Exocytosis treatment of ocular tumor

Xiaofei Wen, Jinfa Ye, Chenyue Qiu, Chengchao Chu et al.
Materials Today Advances
RNA Interference and Gene Delivery
article

Virus-mimetic nanovesicle for the Hijacking- Integration-Vesicular amplification-Exocytosis treatment of ocular tumor

Xiaofei Wen, Jinfa Ye, Chenyue Qiu, Chengchao Chu, Ke Lang, Gang Liu, Pei-Yu Wang, Xingyuan Wei, Yun Han
article en

Abstract

We developed a kind of virus-mimetic nanovesicle (Mel-VSVG-NA), which could react with tumor cells in a membrane fusion procedure (named as First Fusion ), result by the function of Vesicular Stomatitis Virus Glycoprotein (VSVG) in acid microenvironment. Meanwhile, the melittin on Mel-VSVG-NA was transfer on the surface of targeted tumor cell, and thus execute hole-digging process on the tumor cell membrane, causing severe cell content loss and suppression of tumor growth. After the first-round treatment, a harmless ultrasound exposure was carried out, the further engineered vesicles were generated from the damaged cells. Afterwards, the produced vesicles were also confirmed to engineered with VSVG and melittin, which could further fuse with other tumor cells and induced another cell death (named as Second Fusion ). These results indicated that Mel-VSVG-NA is a reliable advance of nano-treatment in ocular tumor therapy, and we bring in this concept of Hijacking- Integration-Vesicular amplification-Exocytosis mode as HIVE therapy. • A Hijacking- Integration-Vesicular amplification-Exocytosis treatment was constructed. • The Mel-VSVG-NA could induce a fusion procedure and execute the hole-digging process, thus induce the cellular damage. • The Mel-VSVG-NA treated MUM-2B cells could in situ produce nanovesicle by an ultrasound stimulation.

Materials Today AdvancesVol. 28
Xiamen University (CN), First Affiliated Hospital of Xiamen University (CN)
Openalex Percentile: Top 72%
RNA Interference and Gene Delivery
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