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Organoids and the Future of Medicine

  • Writer: Han Loke
    Han Loke
  • Aug 7
  • 3 min read

In recent years, organoid technology has transformed the landscape of biomedical science. Derived from a patient’s pluripotent stem cells or adult tissue stem cells, these miniature, three-dimensional structures closely resemble the architecture and function of real human organs. From modelling diseases to testing therapies and enabling personalised treatments, organoids are becoming indispensable tools in modern medicine.


Despite being no larger than a grain of rice and grown in vitro, organoids replicate the complex cellular organisation, microenvironment, and physiological behaviour of tissues like the liver, intestine, brain, pancreas, and lungs. This ability to mimic organ-specific processes has opened up new avenues across regenerative medicine, oncology, genetic disease research, and drug discovery.


🔬 Drug Screening Meets Biology

Organoids make it possible to perform high-throughput drug screening—testing dozens or even hundreds of compounds simultaneously on organoid cultures derived from a specific patient. This is especially crucial in oncology, where cancers often carry unique genetic mutations that influence how they respond to chemotherapy or targeted therapy.

Instead of relying on population-based protocols, treatments can now be individually tailored. Researchers can correlate a patient's genetic mutations, molecular signatures, or biomarkers with how their organoids respond to drugs. This allows for the selection of the most effective, least toxic therapeutic agents, minimising trial-and-error in clinical settings.


Co-Clinical Trials and Living Biobanks

One of the most promising applications of organoids is in co-clinical trials. Here, doctors treat both the patient and their corresponding organoid models simultaneously to compare outcomes. If the organoid shows resistance to a certain drug, it may serve as an early indicator that the treatment will be ineffective in the patient too—thus preventing unnecessary side effects and treatment delays.


Moreover, the creation of organoid biobanks—repositories of living organoids from diverse patient populations—facilitates longitudinal studies and allows for the testing of emerging therapies. These biobanks are particularly valuable for rare diseases or hard-to-study conditions, offering a reusable model system to simulate disease progression and resistance.


Technology Integration: Organoid-on-Chip & Multi-Omics

New technologies are elevating organoid systems to even greater levels of clinical relevance:

  • Organoid-on-chip systems integrate microfluidics and sensors to simulate blood flow, shear stress, and organ-organ interactions. This allows for more realistic modelling of how drugs are absorbed, metabolised, and excreted.


  • Multi-omics integration—combining genomics, transcriptomics, proteomics, and metabolomics—allows researchers to study the entire biological response of an organoid to a treatment. This helps identify new drug targets, refine diagnostics, and monitor resistance development over time.


Together, these tools improve the predictive power of organoid models and support more accurate and adaptive therapeutic strategies.


Why It Matters: From Biology to Better Healthcare

Organoids guide personalised therapy by enabling direct drug testing on patient-derived tissues before treatment is administered. This approach can:

  • Avoid ineffective or toxic treatments

  • Inform therapy adjustments as resistance develops

  • Support adaptive medicine, where care evolves with disease progression

  • Identify optimal therapy combinations and sequences


Relevance to IB biology:

Topic 1: Cell Biology

Organoids are created by growing stem cells into 3D structures that mimic organs. This ties directly into:

  • Cell Differentiation & Specialisation: Organoids develop from pluripotent stem cells, showing how gene expression governs cell fate—essential for understanding embryonic development and tissue formation.

  • Microscopy and Cell Structures: Visualising organoids highlights the importance of microscopy techniques and cellular organisation within tissues.


Topic 2: Molecular Biology

  • Gene Expression: The genetic manipulation of cells to express organ-specific genes shows transcription, translation, and regulation in action.

  • DNA Technology: CRISPR and other tools are used to edit genes in organoids, linking to recombinant DNA and biotechnology topics.


Topic 6: Human Physiology

Organoids model complex organ systems and diseases:

  • Digestive, Nervous, and Endocrine Systems: Intestinal, brain, and pancreatic organoids replicate key organ functions for studying digestion, neural development, and hormone signalling.

  • Medical Applications: Organoids mimic real patient conditions (like cystic fibrosis or cancer), helping students understand how biological systems can fail and how personalised medicine is developed.


Option B: Biotechnology

  • Stem Cells and Cloning: Organoids are created using induced pluripotent stem cells (iPSCs), demonstrating practical uses of stem cell theory.

  • Pharmacogenomics: Organoid models test patient-specific drug responses, aligning with personalised medicine approaches.



References:

1.Organoid-Based Personalized Medicine: From Tumor Outcome Prediction to Autologous Transplantation. Soto-Gamez A, Gunawan JP, Barazzuol L, Pringle S, Coppes RP. Stem Cells (Dayton, Ohio). 2024;42(6):499-508. doi:10.1093/stmcls/sxae023.

2. Patient-Derived Organoids in Precision Medicine: Drug Screening, Organoid-on-a-Chip and Living Organoid Biobank. Zhou Z, Cong L, Cong X. Frontiers in Oncology. 2021;11:762184. doi:10.3389/fonc.2021.762184.

3. Patient-Derived Organoid (PDO) Platforms to Facilitate Clinical Decision Making. Liu L, Yu L, Li Z, Li W, Huang W. Journal of Translational Medicine. 2021;19(1):40. doi:10.1186/s12967-020-02677-2.

4. Patient-Derived Organoids as a Preclinical Platform for Precision Medicine in Colorectal Cancer. Cho YW, Min DW, Kim HP, et al. Molecular Oncology. 2022;16(12):2396-2412. doi:10.1002/1878-0261.13144.


 
 
 

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