Orthotopic Models – Realistic Tumor Microenvironments

Orthotopic models mimic the human disease state more accurately than subcutaneous models by implanting tumor cells or tissue directly into the organ of origin. This preserves the tumor’s interaction with local stroma, vasculature, and immune environment, making these models essential for studying invasion, metastasis, and drug response in a clinically relevant setting.

Why choose orthotopic models?

  • Organ-specific tumor growth: Captures tissue- and site-specific drug responses
  • Natural metastatic behavior: Enables observation of spontaneous or distant-site metastasis
  • Higher predictive value: Better recapitulates clinical efficacy vs. subcutaneous or cell-line-only models
  • Real-time tumor tracking: Bioluminescence and fluorescence imaging for dynamic monitoring of progression and response
  • Supports rare & aggressive cancers: Includes brain metastases, hematologic malignancies, and pretreated tumors

At LIDE, we offer orthotopic models built on PDX, CDX, and hematological tumors, across a wide spectrum of solid and liquid cancers.


Summary of available orthotopic PDX models

Leveraging our best-in-class PDX library, LIDE provides well-characterized orthotopic PDX models—each using luciferase-labeled tumor cells for non-invasive monitoring.

Clinical DiagnosisGenderAgePDX PathologyModel ID
DLBCLF42Diffuse Large B cell LymphomaLD1-0026-410827
Refractory Multiple MyelomaM54Multiple MyelomaLD1-0029-361847
Brain metastasis of breast cancerF64Breast cancer with brain metastasesLD1-2009-362541
Triple-negative breast cancerF38Poorly differentiated adenocarcinomaLD1-2009-362263
AML-M4/5F38Not specifiedLD1-0040-361280
AML-M5M23High-grade lymphoma/leukemiaLD1-0040-362349
AML-M2F57High-grade lymphoma/leukemiaLD1-0040-362393

Analysis and Readouts:

  • IVIS bioluminescent imaging for real-time tracking
  • FACS and molecular profiling for endpoint validation
  • Tumor burden, survival, and toxicity assessment

Summary of available orthotopic CDX models

When patient tissue isn’t available or preferred, LIDE provides well-characterized orthotopic CDX models across multiple organs and tumor types.

IndicationCell LineImplantation SiteSOC Example
GlioblastomaU-87MG-luc, LN229-luc, U251-lucBrain cortex (stereotactic)Temozolomide
Lung AdenocarcinomaA549-luc (orthotopic & metastatic)Lung lobe / lateral veinTrametinib
Colorectal CancerHCT116-lucCecum wall
Hepatocellular CarcinomaHep 3B-lucLiver parenchyma
Pancreatic CancerPANC-1-lucPancreasGemcitabine
Breast Cancer (TNBC)MDA-MB-231-lucMammary fat padGemcitabine
Prostate CancerLNCaP FGC-luc,
PC-3-luc
Dorsal lobe of prostateDocetaxel
Bladder CancerSW780-luc, RT112-lucSW780: (unspecified); RT112: Detrusor & mucosaSW780: Docetaxel; RT112: Sunitinib
Leukemia & LymphomaMV4-11-luc, NALM6-luc, K-562-luc, Raji-lucSystemic (lateral vein)Sunitinib
Murine ModelsGL261-luc, Hepa1-6-luc, H22-lucBrain / LiverTemozolomide, Sorafenib, anti-PD-1, mPD-1

Benefits of using orthotopic CDX Models:

  • Enables rapid proof-of-concept and dose-response studies
  • Supports mechanism-of-action and metastasis tracking
  • Scalable and reproducible: ideal for early screening or validation before PDX scale-up

Model Customization Available:

If your study requires a specific indication, strain, or delivery route, LIDE’s scientific team can support custom orthotopic development on request.

Leverage LIDE’s vast PDX and CDX libraries in an orthotopic environment.


Featured Studies

LN-229-luc Glioblastoma Model
  • Tumor implanted in the brain cortex via stereotactic injection
  • Assessed response to Temozolomide
  • Results: Significant inhibition of tumor progression and metastasis to the spine; monitored via BLI and confirmed through post-mortem analysis
  • Tumor implanted into the bladder mucosa using catheter-based delivery
  • Treated with Docetaxel
  • Results: Reduced tumor radiance and stabilized body weight, confirming therapeutic efficacy

  • Method: Tumor cells derived from PDX tumors are labeled with luciferase and implanted into the mouse brain via stereotactic injection.
  • Endpoints: Tumor growth (via BLI), survival curves, and body weight changes.
  • Use Case: Hematologic malignancies (e.g., AML, DLBCL, Multiple Myeloma).
  • Method: PDX-derived cells are implanted into immunodeficient mice intrafemorally or intravenously after preconditioning.
  • Endpoints: Flow cytometry (FACS) tracking of tumor burden via specific immune cell markers (e.g., CD45+, CD33+, CD19+, CD38+).