# Phytochemical Profile and Selective Anticancer Activity of Parietaria judaica L. Extracts

**Authors:** Izabela Bielecka, Dorota Natorska-Chomicka, Wioleta Dołomisiewicz, Arlindo Rodrigues Fortes, Katarzyna Dos Santos Szewczyk

PMC · DOI: 10.3390/molecules30132739 · 2025-06-25

## TL;DR

This study explores Parietaria judaica as a natural source of anticancer compounds, showing that its ethanolic extract is effective against cancer cells while being less toxic to normal cells.

## Contribution

The study identifies the ethanolic extract of Parietaria judaica as a selective anticancer agent with potential for further therapeutic development.

## Key findings

- The ethanolic extract (PJ-E) showed strong cytotoxicity against HeLa cells with an IC50 of 11.82 µg/mL.
- PJ-E had significantly higher IC50 (139.42 µg/mL) against noncancerous HEK-293 cells, indicating tumor selectivity.
- The water extract (PJ-W) showed selective activity against lung cancer cells with minimal toxicity toward normal cells.

## Abstract

Parietaria judaica L. (alfavaca-de-cobra) was investigated as a potential source of anticancer compounds. Leaf extracts obtained using solvents of different polarities were evaluated for their phytochemical profiles and cytotoxic activities against a panel of human cancer cell lines (glioblastoma LN-229, lung NCI-H1563, breast MDA-MB-231, liver HepG2, renal 769-P, cervical HeLa, and melanoma A-375) and a noncancerous HEK-293 cell line. LC-ESI-MS/MS analysis confirmed that the extracts are rich in polyphenols, including phenolic acids and flavonoids. Cytotoxicity was assessed via MTT and SRB assays, demonstrating dose-dependent antiproliferative effects. Among the extracts, the ethanolic fraction (PJ-E) exhibited the strongest cytotoxicity, with an IC50 of 11.82 µg/mL against HeLa cells, while displaying a significantly higher IC50 (139.42 µg/mL) against HEK-293, indicating tumor selectivity. The water extract (PJ-W) showed selective activity against lung cancer cells (IC50 = 87.69 µg/mL), with minimal toxicity toward normal cells. The methanol/acetone extract (PJ-M) displayed intermediate activity, whereas the hexane extract (PJ-H) was the least effective. These findings highlight P. judaica, particularly its ethanolic extract, as a promising source of natural anticancer agents. Further research focusing on the isolation of active constituents, formulation development, and in vivo validation is warranted to support its therapeutic potential.

## Linked entities

- **Diseases:** glioblastoma (MONDO:0018177), lung cancer (MONDO:0005138), breast cancer (MONDO:0004989), liver cancer (MONDO:0002691), renal cancer (MONDO:0005206), cervical cancer (MONDO:0002974), melanoma (MONDO:0005105)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** lung cancer (MESH:D008175), cancer (MESH:D009369), glioblastoma (MESH:D005909), melanoma A-375 (MESH:D008545), Cytotoxicity (MESH:D064420)
- **Chemicals:** water (MESH:D014867), flavonoids (MESH:D005419), polyphenols (MESH:D059808), PJ-E (-), phenolic acids (MESH:C017616), acetone (MESH:D000096), MTT (MESH:C070243), methanol (MESH:D000432), hexane (MESH:D006586)
- **Species:** Homo sapiens (human, species) [taxon 9606], Parietaria judaica (species) [taxon 33127]
- **Cell lines:** HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030), HEK-293 — Homo sapiens (Human), Transformed cell line (CVCL_0045), renal 769-P — Homo sapiens (Human), Renal cell carcinoma, Cancer cell line (CVCL_1050), NCI-H1563 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_1475), MDA-MB-231 — Homo sapiens (Human), Breast adenocarcinoma, Cancer cell line (CVCL_0062), HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027), LN-229 — Homo sapiens (Human), Glioblastoma, Cancer cell line (CVCL_0393)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12251272/full.md

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Source: https://tomesphere.com/paper/PMC12251272