banner
Custom In Vivo Tumor Model Services
Online Inquiry

JURL-MK1 Xenograft Model Service for CML

JURL-MK1 Xenograft Model Service for CML

The JURL-MK1 cell line provides a highly specialized and translationally relevant in vivo platform for investigating the molecular complexities of Chronic myeloid leukemia (CML), particularly in the blast crisis phase. As a premier pre-clinical contract research organization, Alfa Cytology delivers an integrated, high-precision JURL-MK1 Xenograft Model Service, meticulously optimized to provide reproducible, audit-ready data packages that accelerate your CML drug discovery and development pipeline.

Overview of JURL-MK1 Xenograft Model for CML

The JURL-MK1 xenograft model is an established in vivo translational system widely utilized in hematological oncology research for the study of CML. By transplanting human JURL-MK1 myeloid cells into highly permissive, immunodeficient rodent hosts, this model effectively reproduces the systemic dissemination, bone marrow homing kinetics, and peripheral blood pathophysiological profiles characteristic of progressive human CML.

Biologically, the JURL-MK1 model is highly valued for its consistent engraftment profiles and predictable disease progression, which provide investigators with a reliable experimental window for evaluating complex dosing schedules and pharmacodynamics. This model preserves critical human myeloid molecular features, including lineage-specific marker expression and intracellular signaling pathways that drive blast expansion. Consequently, the JURL-MK1 model is extensively deployed in pre-clinical screening programs to assess the anti-leukemic potency of novel small-molecule inhibitors, targeted monoclonal antibodies, and combination therapeutic regimens in a physiologically relevant in vivo setting.

Percentage cell viability in CML cell lines KU812, Lama84, KYO-1, JURL-MK1, EM2, and KLC22, treated with imatinib for 48 h; Imatinib IC-50 for each cell line is depicted (right)Fig 1. Percentage cell viability in CML cell lines KU812, Lama84, KYO-1, JURL-MK1, EM2, and KLC22, treated with imatinib for 48 h; Imatinib IC-50 for each cell line is depicted (right). (Rajamani BM, et al., 2023)

Cell Line Information: JURL-MK1

The JURL-MK1 cell line is derived from a patient diagnosed with CML in the blast crisis phase. These cells grow as suspension cultures under standard in vitro laboratory parameters, maintaining a stable myeloblastic phenotype that serves as a robust proxy for hematological cancer research.

Attribute Details
Cell Line Name JURL-MK1
Organism Homo sapiens (Human)
Tissue/Origin Peripheral blood
Disease/Pathology Chronic myeloid leukemia (CML)
Genetic Features BCR-ABL1 positive; Philadelphia chromosome positive
Morphology Myeloblast
Growth Properties Suspension
Biosafety Level BSL-1 / BSL-2 (Depending on regional institutional guidelines)
Applications In vitro drug sensitivity screening, in vivo xenograft tracking, target validation, and therapeutic efficacy testing

Our Services

Workflow of JURL-MK1 Xenograft Model Construction

  • Cell Culture & Quality Control: Human JURL-MK1 cells are expanded in vitro using certified nutrient suspension media under optimized growth parameters. STR authentication and mycoplasma clearance verification are completed prior to inoculation to ensure absolute phenotypic identity and biological purity.
  • Host Selection & Acclimatization: Standardized, healthy immunodeficient mice are sourced from validated vendors. The animals undergo a dedicated acclimatization phase to stabilize baseline biological and physiological metrics.
  • Precision Inoculation: A calibrated suspension of high-viability JURL-MK1 cells is prepared in a sterile physiological buffer. The cellular suspension is precisely inoculated in vivo into the host cohorts via tail vein intravenous routes to facilitate systemic leukemic distribution.
  • Longitudinal Growth Tracking: Following inoculation, disease progression is systematically monitored using FACS to detect human CD45+ cells or specific myeloid markers in peripheral blood. Animal weight, physical clinical indicators, and systemic disease burden are documented routinely.
  • Stratification & Dosing: Once peripheral leukemic chimerism reaches a predetermined, statistically optimal range, the mice are randomized into matched experimental cohorts to ensure balanced baseline systemic dimensions before the initiation of customized therapeutic dosing regimens.

JURL-MK1 Xenograft Model Construction WorkflowFig 2. JURL-MK1 Xenograft Model Construction Workflow

Case Study - JURL-MK1 Xenograft Model Development

A pre-clinical validation study was conducted using the JURL-MK1 xenograft model to evaluate the therapeutic efficacy of a novel targeted inhibitor designed for CML. Following precision intravenous inoculation of human JURL-MK1 cells into immunodeficient mice, the animals exhibited steady, systemic leukemic engraftment and highly predictable disease progression across all study cohorts. Animals assigned to the active treatment group demonstrated a clear, statistically significant reduction in circulating leukemic blasts and prolonged survival times compared to the vehicle control, confirming the model's high sensitivity and predictive reliability for screening targeted CML therapies.

Case Study - JURL-MK1 Xenograft Model Development

Why Choose Alfa Cytology?

  • Oncology Domain Expertise: Profound experience in managing diverse hematological and myeloid lineages, providing highly reproducible in vivo translational platforms for complex leukemia research.
  • Rigorous Quality Control: Meticulous cell validation and standardized operating procedures that minimize experimental variability across all project stages.
  • Tailored Experimental Design: Highly flexible protocols that adapt to specific animal strain requirements, custom dosing schedules, and unique compound properties.
  • High-Resolution Deliverables: Every project concludes with a detailed, audit-ready data report providing comprehensive digital caliper metrics and robust statistical validations.

Contact us

Accelerating your CML pipeline requires a pre-clinical partner with the technical proficiency to execute rigorous in vivo workflows flawlessly. If you are looking to advance your novel compound or require specialized pre-clinical testing using our JURL-MK1 platform, please reach out to us today to discuss your project requirements with our expert scientific team.

Reference

  1. Rajamani BM, et al. Modulating retinoid-X-receptor alpha (RXRA) expression sensitizes chronic myeloid leukemia cells to imatinib in vitro and reduces disease burden in vivo. Front Pharmacol. 2023 May 31;14:1187066.

For research use only. Not intended for any clinical use.

Related Services

Adrenal Cancer
Breast Cancer
Biliary Tract Cancer
Head and Neck Cancer
Bladder Cancer
Cervical Cancer
Glioblastoma
Retinoblastoma
Medulloblastoma
Colon Cancer
Endometrial Cancer
Gastric Cancer
Epidermoid Carcinoma
Esophageal Adenocarcinoma (EAC)
Esophageal Squamous Cell Carcinoma (ESCC)
Ewing's Sarcoma
AML
CML
ALL
Leukemia
Liver Cancer
Prostate Cancer
NSCLC