# In vitro assessment of Moringa Oleifera leaf extract’s protective impact on fibroblast cell line (WI-38) exposed to electronic cigarette liquid

**Authors:** Raneem F. Obeid, Yara Y. Mouselhy, Mona Eltaher, Radwa T. El-sharkawy

PMC · DOI: 10.1038/s41598-025-14513-y · Scientific Reports · 2025-08-16

## TL;DR

This study shows that Moringa Oleifera leaf extract can cause cell death in lung cells exposed to e-cigarette liquid, suggesting it may act as an anti-proliferative agent.

## Contribution

The study reveals the anti-proliferative potential of Moringa Oleifera leaf extract against e-cigarette liquid toxicity in fibroblast cells.

## Key findings

- MOLE induced apoptosis in EC e-liquid treated WI-38 cells by up-regulating Bax and down-regulating Bcl2.
- MOLE caused cell cycle arrest at the S phase in treated cells.
- MOLE was ineffective as a cytoprotective agent but showed cytotoxic effects.

## Abstract

Moringa oleifera (MO), a medicinal herb, has been studied in recent decades for its diverse range of biological activities. Several studies have revealed that MO leaf extract (MOLE) possesses cytoprotective properties, while other studies have reported anti-proliferative potential. This study was conducted to assess the potential effect of MOLE on electronic cigarette liquid (EC e-liquid) treated human lung fibroblast cell line (WI-38). An MTT assay was performed to investigate the potential effect of EC e-liquid and MOLE on cell viability and determine the cytotoxic concentration (CC50) in WI-38 cells. Cells were treated with 190.2 µg/mL of EC e-liquid (EC group) and 33.2 µg/mL of EC e-liquid and MOLE (EC + MOLE group) for 24 h. Analysis of apoptosis and cell cycle was performed using flow cytometric assay. Moreover, the expression of apoptosis-related proteins Bax and Bcl2 was measured using ELISA.Our findings revealed that MOLE demonstrated a cytotoxic effect on EC e-liquid treated WI-38 cells through induction of apoptosis via up-regulation of Bax and down-regulation of Bcl2. Additionally, MOLE induced cell cycle arrest at the S phase. Overall, these findings indicate that MOLE is an inefficient cytoprotective agent against EC e-liquid cytotoxicity; nonetheless, it exerts a cytotoxic effect, suggesting a promising role as a valuable anti-proliferative agent.

## Linked entities

- **Proteins:** BAX (BCL2 associated X, apoptosis regulator), BCL2 (BCL2 apoptosis regulator)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CCNL2 (cyclin L2) [NCBI Gene 81669] {aka ANIA-6B, CCNM, CCNS, HCLA-ISO, HLA-ISO, PCEE}, CDKN1A (cyclin dependent kinase inhibitor 1A) [NCBI Gene 1026] {aka CAP20, CDKN1, CIP1, MDA-6, P21, SDI1}, CDK2 (cyclin dependent kinase 2) [NCBI Gene 1017] {aka CDKN2, p33(CDK2)}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, ANXA5 (annexin A5) [NCBI Gene 308] {aka ANX5, CPB-I, ENX2, HEL-S-7, PP4, RPRGL3}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}
- **Diseases:** breast cancer (MESH:D001943), necrosis (MESH:D009336), melanoma (MESH:D008545), carcinogenic (MESH:D011230), Cytotoxicity (MESH:D064420), cancer (MESH:D009369)
- **Chemicals:** beta-carotene (MESH:D019207), FITC (MESH:D016650), chromium (MESH:D002857), EDTA (MESH:D004492), tocopherol (MESH:D024505), PI (MESH:D010716), potassium (MESH:D011188), glycerin (MESH:D005990), HEPES (MESH:D006531), flavonoid (MESH:D005419), phenolic acids (MESH:C017616), iron (MESH:D007501), Quercetin (MESH:D011794), PBS (MESH:D007854), alkaloids (MESH:D000470), calcium (MESH:D002118), alcohol (MESH:D000438), cadmium (MESH:D002104), acetone (MESH:D000096), ethanol (MESH:D000431), DMSO (MESH:D004121), uranyl acetate (MESH:C005460), water (MESH:D014867), copper (MESH:D003300), ROS (MESH:D017382), MTT (MESH:C070243), steroids (MESH:D013256), aluminum (MESH:D000535), acetaldehyde (MESH:D000079), tannins (MESH:D013634), sterols (MESH:D013261), nitrosamines (MESH:D009602), osmium tetroxide (MESH:D009993), 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MESH:C022616), L-glutamine (MESH:D005973), Nicotine (MESH:D009538), CO2 (MESH:D002245), PG (MESH:D019946), formaldehyde (MESH:D005557), terpenoids (MESH:D013729), nickel (MESH:D009532), DMEM (-), glutaraldehyde (MESH:D005976), epoxy resin (MESH:D004853), silicon (MESH:D012825), kaempferol (MESH:C006552), glycol (MESH:D006018), gentamycin (MESH:D005839), alkanes (MESH:D000473), C (MESH:D002244)
- **Species:** Homo sapiens (human, species) [taxon 9606], Moringa oleifera (horseradish tree, species) [taxon 3735], Nicotiana tabacum (American tobacco, species) [taxon 4097], Microbacterium sp. O (species) [taxon 2502250]
- **Cell lines:** MO-522 — Homo sapiens (Human), Xeroderma pigmentosum, complementation group C, Finite cell line (CVCL_M231), WI-38 — Homo sapiens (Human), Finite cell line (CVCL_0579)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12357913/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12357913/full.md

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Source: https://tomesphere.com/paper/PMC12357913