# Nanotechnology-Enabled Precision Therapy for Lung Cancer in Never-Smokers

**Authors:** Cristian Cojocaru, Adina Magdalena Țurcanu, Ruxandra Cojocaru, Elena Cojocaru

PMC · DOI: 10.3390/pharmaceutics18020161 · 2026-01-26

## TL;DR

This paper reviews how nanotechnology can improve targeted therapies for lung cancer in people who have never smoked, by overcoming biological barriers and resistance issues.

## Contribution

The paper introduces nanocarrier-based strategies to enhance drug delivery and address resistance in lung cancer in never-smokers.

## Key findings

- Nanocarriers can improve drug solubility, circulation, and targeting in lung cancer in never-smokers.
- Combining TKIs with nucleic acid-based therapies via nanocarriers may help overcome resistance mechanisms.
- Successful clinical translation depends on biomarker-guided patient selection and scalable manufacturing.

## Abstract

Lung cancer in never-smokers (LCINS) represents a distinct clinical entity driven by dominant oncogenic alterations and characterized by a low tumor mutational burden. Although tyrosine kinase inhibitors (TKIs) achieve high initial response rates, their long-term efficacy is limited by suboptimal pharmacokinetics, restricted central nervous system (CNS) penetration, tumor microenvironment barriers, and acquired resistance. In this review, we critically assess the current state of nanotechnology-assisted drug delivery systems for LCINS, with a primary focus on how rationally designed nanocarriers can overcome biological barriers, enable molecular subtype-specific therapeutic strategies, and address mechanisms that limit clinical efficacy and durability of response. We conducted a structured literature search using PubMed and Web of Science (January 2022 to November 2025), focusing on primary studies reporting the preparation, physicochemical properties, and therapeutic performance of nanocarriers in in vitro and in vivo models, as well as available pharmacokinetic and clinical data. LCINS is characterized by inefficient vasculature, high extracellular matrix density, active efflux transporters, and immunosuppressive niches, and is frequently complicated by brain metastases. Nanocarrier-based platforms can enhance aqueous solubility, prolong systemic circulation, and improve tumor or CNS targeting. Co-delivery systems combining TKIs with nucleic acid-based therapeutics, together with stimuli-responsive platforms, offer the potential for simultaneous modulation of multiple oncogenic pathways and partial mitigation of resistance mechanisms. In summary, nanotechnology provides a promising strategy to improve both the efficacy and specificity of targeted therapies in LCINS. Successful clinical translation will depend on biologically aligned carrier–payload combinations, scalable and reproducible manufacturing processes, and biomarker-guided patient selection.

## Linked entities

- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}, TAT (tyrosine aminotransferase) [NCBI Gene 6898], Met (MET proto-oncogene, receptor tyrosine kinase) [NCBI Gene 24553] {aka Hgfr}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, ROS1 (ROS proto-oncogene 1, receptor tyrosine kinase) [NCBI Gene 6098] {aka MCF3, ROS, c-ros-1}, TFRC (transferrin receptor) [NCBI Gene 7037] {aka CD71, IMD46, T9, TFR, TFR1, TR}, Ros1 (ROS proto-oncogene 1 , receptor tyrosine kinase) [NCBI Gene 25346] {aka ROS1C}, Trf (transferrin) [NCBI Gene 22041] {aka Cd176, HP, Tf, Tfn, hpx}, DNER (delta/notch like EGF repeat containing) [NCBI Gene 92737] {aka UNQ26, bet}, KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, HDAC9 (histone deacetylase 9) [NCBI Gene 9734] {aka HD7, HD7b, HD9, HDAC, HDAC7B, HDAC9B}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, EML4 (EMAP like 4) [NCBI Gene 27436] {aka C2orf2, ELP120, EMAP-4, EMAPL4, ROPP120}, ABCG2 (ATP binding cassette subfamily G member 2 (JR blood group)) [NCBI Gene 9429] {aka ABC15, ABCP, BCRP, BMDP, CD338, CDw338}, Kras (KRAS proto-oncogene, GTPase) [NCBI Gene 24525] {aka K-ras, Kras2, c-Ki-ras, p21}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, SLTM (SAFB like transcription modulator) [NCBI Gene 79811] {aka Met}, Alk (ALK receptor tyrosine kinase) [NCBI Gene 266802], EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, Hgf (hepatocyte growth factor) [NCBI Gene 24446] {aka HPTA}, PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 5243] {aka ABC20, CD243, CLCS, ENPAT, GP170, MDR1}, SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, Ret (ret proto-oncogene) [NCBI Gene 24716], Pik3cg (phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma) [NCBI Gene 298947] {aka Pi3k}, MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313] {aka CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1}, Egfr (epidermal growth factor receptor) [NCBI Gene 24329] {aka ERBB1, ErbB-1, Errp}, Tfrc (transferrin receptor) [NCBI Gene 22042] {aka 2610028K12Rik, CD71, E430033M20Rik, Mtvr1, TFR, TFR1}, FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, RET (ret proto-oncogene) [NCBI Gene 5979] {aka CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1}, PGP (phosphoglycolate phosphatase) [NCBI Gene 283871] {aka AUM, G3PP, PGPase}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, Egfr (epidermal growth factor receptor) [NCBI Gene 13649] {aka 9030024J15Rik, Erbb, Errb1, Errp, Wa5, wa-2}, LRP1 (LDL receptor related protein 1) [NCBI Gene 4035] {aka A2MR, APOER, APR, CD91, DDH3, IGFBP-3R}, STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}
- **Diseases:** metastases (MESH:D009362), thrombus (MESH:D013927), cytotoxic (MESH:D064420), involvement (MESH:C564676), coronavirus disease 2019 (MESH:D000086382), solid (MESH:D018250), prostate (MESH:D011472), Brain metastases (MESH:D001932), glioblastoma (MESH:D005909), glioma (MESH:D005910), injury to (MESH:D014947), intracranial disease (MESH:D020765), cancer (MESH:D009369), adenocarcinoma (MESH:D000230), Lung (MESH:D008171), LCINS (MESH:D008175), hypoxic (MESH:D002534), hypoxia (MESH:D000860), NSCLC (MESH:D002289), hyperthermia (MESH:D005334)
- **Chemicals:** disulfide (MESH:D004220), patritumab (MESH:C585471), entrectinib (MESH:C000607349), poloxamers (MESH:D020442), lorlatinib (MESH:C000590786), Silica (MESH:D012822), doxorubicin (MESH:D004317), brigatinib (MESH:C000598580), taletrectinib (MESH:C000720459), BDTX-1535 (-), arginine (MESH:D001120), dacomitinib (MESH:C525726), selpercatinib (MESH:C000656166), gefitinib (MESH:D000077156), Lipid (MESH:D008055), poziotinib (MESH:C557213), trastuzumab deruxtecan (MESH:C000614160), poly(amidoamine) (MESH:C531249), erlotinib (MESH:D000069347), GSH (MESH:D005978), afatinib (MESH:D000077716), savolitinib (MESH:C000593259), glycerides (MESH:D005989), poly(beta amino ester) (MESH:C507253), BIND-014 (MESH:D000077143), Dendrimers (MESH:D050091), poly(lactic-co-glycolic acid) (MESH:D000077182), poly(ethylene imine) (MESH:C505405), alginate (MESH:D000464), osimertinib (MESH:C000596361), Chitosan (MESH:D048271), acid (MESH:D000143), deoxy (MESH:C038782), ramucirumab (MESH:C543333), tepotinib (MESH:C000707607), polymer (MESH:D011108), waxes (MESH:D014885), PEG (MESH:D011092), paclitaxel (MESH:D017239), polysaccharide (MESH:D011134), bortezomib (MESH:D000069286), isoliquiritigenin (MESH:C040920), Alectinib (MESH:C582670), almonertinib (MESH:C000718108), pyrotinib (MESH:C000622954), Doxil (MESH:C506643), tyrosine (MESH:D014443), pralsetinib (MESH:C000655704), phospholipid (MESH:D010743), hyaluronic acid (MESH:D006820), repotrectinib (MESH:C000708510), bevacizumab (MESH:D000068258), mitoxantrone (MESH:D008942), copper (MESH:D003300), capmatinib (MESH:C000613976), furmonertinib (MESH:C000705711)
- **Species:** Homo sapiens (human, species) [taxon 9606], Bacteriophage sp. (species) [taxon 38018], Mus musculus (house mouse, species) [taxon 10090], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Nicotiana tabacum (American tobacco, species) [taxon 4097]
- **Mutations:** C797S, D1203N, G810R/S, D1228H, G2032R, G810R, L1196M, L858R, G1202R, T790M
- **Cell lines:** A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), H1975 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_1511)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12944088/full.md

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Source: https://tomesphere.com/paper/PMC12944088