# Natural products as kinase inhibitors in lung cancer: molecular mechanisms, therapeutic potential, and clinical trials

**Authors:** Adil Farooq Wali, Sirajunisa Talath, Rasha Babiker, Mohamed El-Tanani, Imran Rashid Rangraze, Walaa Ibraheem, Yusra Al Aldhaheri, Shakta Mani Satyam, Yahia El-Tanani

PMC · DOI: 10.3389/fphar.2026.1764550 · 2026-02-25

## TL;DR

Natural products may offer safer and more effective lung cancer treatments by targeting multiple kinases involved in tumor growth and resistance.

## Contribution

This review highlights the potential of natural kinase inhibitors as multi-targeted, less toxic alternatives to synthetic drugs in lung cancer therapy.

## Key findings

- Natural kinase inhibitors like curcumin and resveratrol modulate key cancer pathways such as EGFR and MAPK.
- Preclinical and emerging clinical evidence supports the use of natural products as adjuncts or alternatives to conventional therapies.
- Challenges include poor solubility and limited clinical validation, requiring formulation optimization and large-scale trials.

## Abstract

Lung cancer remains a leading cause of cancer mortality worldwide, with current treatments often limited by toxicity and resistance. Dysregulated kinase signaling particularly involving EGFR, PI3K/AKT/mTOR, MAPK, and ALK pathways drives tumor growth, survival, and metastasis. While synthetic kinase inhibitors have improved outcomes, their use is constrained by adverse effects and acquired resistance. Natural kinase inhibitors (NKIs) derived from plants, marine organisms, and microorganisms offer a promising alternative due to their multi-targeted action, lower toxicity, and potential to overcome resistance. This review aims to evaluate the molecular mechanisms, therapeutic potential, and clinical relevance of NKIs in lung cancer management. Key compounds such as curcumin, resveratrol, quercetin, genistein, and epigallocatechin gallate inhibit critical kinases, modulating pathways that regulate proliferation, apoptosis, angiogenesis, and metastasis. Preclinical studies demonstrate significant anticancer activity, while emerging clinical evidence supports their role as adjuncts or alternatives to conventional therapies. Strategies such as nanotechnology-based delivery systems and combination regimens further enhance bioavailability and efficacy. Despite these advantages, challenges persist, including poor solubility, rapid metabolism, and limited clinical validation. Future research should focus on optimizing formulations, elucidating pharmacokinetics, and conducting large-scale clinical trials to confirm safety and effectiveness. Integration of NKIs into personalized treatment paradigms could transform lung cancer therapy, offering cost-effective, less toxic, and multi-targeted approaches to improve patient outcomes.

## Linked entities

- **Proteins:** EGFR (epidermal growth factor receptor), PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha), AKT1 (AKT serine/threonine kinase 1), MTOR (mechanistic target of rapamycin kinase), MAPK (mitogen activated kinase-like protein), ALK (ALK receptor tyrosine kinase)
- **Chemicals:** curcumin (PubChem CID 969516), resveratrol (PubChem CID 5056), quercetin (PubChem CID 5280343), genistein (PubChem CID 5280961), epigallocatechin gallate (PubChem CID 1287)
- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}
- **Diseases:** metastasis (MESH:D009362), toxicity (MESH:D064420), cancer (MESH:D009369), Lung cancer (MESH:D008175)
- **Chemicals:** curcumin (MESH:D003474), genistein (MESH:D019833), resveratrol (MESH:D000077185), epigallocatechin gallate (MESH:C045651), quercetin (MESH:D011794)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

50 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12975763/full.md

---
Source: https://tomesphere.com/paper/PMC12975763