# Organoids: technology refining, current applications and future directions

**Authors:** Xianda Cheng, Ziqi Fang, Jianhui Sun, Liyu Liu, Yan Yang, Junyi Wang, Jianwei Shuai, Xikun Zhou, Ping Lin, Gen Yang, Xiuli Bi, Min Wu

PMC · DOI: 10.1186/s43556-026-00422-7 · Molecular Biomedicine · 2026-03-14

## TL;DR

Organoids are miniature organ models used for studying diseases and testing treatments, with promising applications in cancer research and drug development.

## Contribution

The paper reviews recent advances in organoid culture and highlights their potential for precise cancer modeling and immunotherapy.

## Key findings

- Organoids are being used for disease modeling, drug screening, and testing treatment responses.
- Immune organoids are valuable for understanding drug resistance and guiding drug development.
- Organoid-on-chip technologies simulate real organ environments for improved research accuracy.

## Abstract

Organoids are derived from pluripotent stem cells or tissue stem cells, progenitor cells, or differentiated cells from healthy or diseased tissues (e.g., tumors). Numerous organoid engineering strategies have been tested to support the culture, growth, proliferation, differentiation, and maturation of organoids. A variety of organoids and organoid-on-chips have also been constructed to reflect real environments of human and mouse organs. Currently, four major areas of potential application for organoids include disease modeling, anticancer drug screening, drug toxicology testing, and gene/cell therapy. For cancer immunotherapy, immune organoids based on co-culturing human tumor cells have been used as a critical platform for drug screening and targeted therapy. This review summarizes recent advances in organoid culture, lists the methods for constructing organoids and their main applications, and highlights its value as a tool for precise cancer modeling. Given the enormous potential of organoids as an in vitro culture model in cancer treatment, we also discussed organoid-based methods for angiogenesis and immune microenvironment modeling, and analyzed the wide range of applications of immune organoids, such as testing treatment response, exploring mechanisms of drug resistance, optimizing treatment strategies, and guiding drug development. Finally, we attempt to look into the critical challenges and bright prospects for cancer organoid research.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)
- **Species:** Homo sapiens (taxon 9606), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, LGR5 (leucine rich repeat containing G protein-coupled receptor 5) [NCBI Gene 8549] {aka FEX, GPR49, GPR67, GRP49, HG38}, AURKA (aurora kinase A) [NCBI Gene 6790] {aka AIK, ARK1, AURA, BTAK, PPP1R47, STK15}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, MSLN (mesothelin) [NCBI Gene 10232] {aka MPF, SMRP}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, GPC3 (glypican 3) [NCBI Gene 2719] {aka DGSX, GTR2-2, MXR7, OCI-5, SDYS, SGB}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, TBK1 (TANK binding kinase 1) [NCBI Gene 29110] {aka AIARV, FTDALS4, IIAE8, NAK, T2K}
- **Diseases:** SCLC (MESH:D018288), solid (MESH:D018250), hematologic malignancies (MESH:D019337), CeD (MESH:D002446), inflammation (MESH:D007249), hereditary copper poisoning (MESH:D009386), liver disease (MESH:D008107), breast cancer (MESH:D001943), asthma (MESH:D001249), necrosis (MESH:D009336), Wilson's disease (MESH:D006527), lymphoma (MESH:D008223), hypoxia (MESH:D000860), MOS (MESH:C536681), cystic fibrosis (MESH:D003550), ulcerative colitis (MESH:D003093), fibrosis (MESH:D005355), multiple sclerosis (MESH:D009103), Cancer (MESH:D009369), Crohn's disease (MESH:D003424), viral infection (MESH:D014777), melanoma (MESH:D008545), liver toxicity (MESH:D056486), autoimmune (MESH:D001327), psoriasis (MESH:D011565), CRC (MESH:D015179), end-stage diseases (MESH:D007676), Huntington's disease (MESH:D006816), cytotoxicity (MESH:D064420), gastric cancer (MESH:D013274), hepatocellular carcinoma (MESH:D006528), microcephaly (MESH:D008831), autism (MESH:D001321), metastasis (MESH:D009362), lung cancer (MESH:D008175), carcinogenesis (MESH:D063646), PKD (MESH:D007690), TNBC (MESH:D064726), PDAC (MESH:D021441), IBD (MESH:D015212), HIV infection (MESH:D015658), infection (MESH:D007239), Small-cell lung cancer (MESH:D055752)
- **Chemicals:** water (MESH:D014867), oil (MESH:D009821), heparin (MESH:D006493), platinum (MESH:D010984), oxygen (MESH:D010100), Cet-ZA (-)
- **Species:** Canis lupus familiaris (dog, subspecies) [taxon 9615], Homo sapiens (human, species) [taxon 9606], Comamonas testosteroni (species) [taxon 285], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** Vd2 — Homo sapiens (Human), Finite cell line (CVCL_S042)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12988128/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12988128/full.md

## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12988128/full.md

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Source: https://tomesphere.com/paper/PMC12988128