# Anti-cancer activity of 7-methoxyheptaphylline from Clausena harmandiana against PANC-1 pancreatic cancer cells and its sustainable extraction method

**Authors:** Juthamart Maneenet, Suresh Awale, Chantana Boonyarat, Pornthip Waiwut, Rawiwun Kaewamatawong

PMC · DOI: 10.1371/journal.pone.0334901 · PLOS One · 2025-10-16

## TL;DR

This study shows that 7-methoxyheptaphylline from Clausena harmandiana effectively targets pancreatic cancer cells and can be sustainably extracted using ultrasound.

## Contribution

The study introduces a sustainable extraction method for 7-methoxyheptaphylline and demonstrates its anti-cancer activity under nutrient-deprived conditions.

## Key findings

- 7-MH showed selective cytotoxicity against PANC-1 cells with minimal toxicity to normal cells.
- The compound inhibited wound closure and colony formation, indicating anti-metastatic potential.
- 7-MH suppressed the PI3K/Akt/mTOR pathway, especially under nutrient deprivation.

## Abstract

Pancreatic cancer presents a significant therapeutic challenge characterized by poor survival rates, leading to development of innovative treatment strategies. This study evaluated the anti-cancer potential of 7-methoxyheptaphylline (7-MH), a carbazole alkaloid from Clausena harmandiana, against pancreatic cancer cells (PANC-1) and developed an environmentally sustainable extraction methodology using ultrasonic-assisted extraction (UAE). 7-MH demonstrated selective cytotoxicity against PANC-1 cells with preferential activity under nutrient deprivation conditions (PC50 = 4.54 μM) compared to nutrient-rich conditions (IC50 = 46.84 μM). This compound exhibited minimal toxicity toward normal MCE301 epithelial cells (IC50 = 83.4 μM). Live-cell imaging showed dose-dependent apoptotic morphology including membrane blebbing and cell shrinkage within 24 hours. At concentrations of 25 and 50 μM, the compound significantly inhibited wound closure and colony formation, suggesting antimetastatic properties. Mechanistic analysis exhibited that 7-MH suppressed the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt)/mammalian target of rapamycin (mTOR) signaling pathway specially under nutrient deprived conditions. Western blot analysis showed 45% reduction in Akt expression, 43% decrease in mTOR phosphorylation, and complete inhibition of Akt phosphorylation at 20 µM concentration. For sustainable extraction of 7-MH, UAE using ethanol was optimized through response surface methodology (RSM) with central composite design (CCD). The optimal protocol (50 °C, 60 minutes, 0.40 g/10 mL plant/solvent ratio) achieved 1.26 ± 0.02% yield with only 3.55% deviation from predicted values. This developed extraction method provides an efficient and environmentally sustainable alternative to conventional halogenated solvent extraction methods. These findings offer valuable insights for advancing natural product-based cancer therapeutics and demonstrate the implementation of sustainable natural products extraction principles.

## Linked entities

- **Proteins:** PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha), AKT1 (AKT serine/threonine kinase 1), MTOR (mechanistic target of rapamycin kinase)
- **Chemicals:** 7-methoxyheptaphylline (PubChem CID 189688), ethanol (PubChem CID 702)
- **Diseases:** pancreatic cancer (MONDO:0005192)
- **Species:** Clausena harmandiana (taxon 159036)

## Full-text entities

- **Genes:** PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}
- **Diseases:** Pancreatic cancer (MESH:D010190), cancer (MESH:D009369), cytotoxicity (MESH:D064420)
- **Chemicals:** carbazole alkaloid (-), ethanol (MESH:D000431), 7-MH (MESH:C557425)
- **Cell lines:** MCE301 — Mus musculus (Mouse), Conditionally immortalized cell line (CVCL_6B09), PANC-1 — Homo sapiens (Human), Pancreatic ductal adenocarcinoma, Cancer cell line (CVCL_0480)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12530583/full.md

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12530583/full.md

## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12530583/full.md

---
Source: https://tomesphere.com/paper/PMC12530583