Tumour model

MBT-2

Carcinoma
SyngeneicIn vitroResistant

Standard of Care sensibility: Anti-PD1 = no / Anti PDL1 = yes (12,5 mg/kg)

Acquired resistance to: PDL1

 

MBT-2 cells 

Mouse MBT-2 cells are derived from C3H/He bladder transitional cells serially transplanted and  exposed to FANFT 

Tumour growth in vivo 

The cells were collected from a tissue culture flask and injected subcutaneously in the right flank of  C3H/He mice. The resulting tumours were monitored by measuring two diameters with calipers, and extrapolating the volume to a sphere.  

The mice bearing MBT-2 tumours can be treated by intra-peritoneal, intra-venous, intra-tumoral  or subcutaneous injection of the compounds. Per os administration is also possible.  

Figure 1: (View PDF)

Tumour growth curve of the MBT-2 cells as  subcutaneous tumours Mean ± SEM (n=4; take rate 100%) 

Drug Responses 

Anti-PD1 12.5 mg/kg → No reponse
Anti-PDL1 12.5 mg/kg → Response 

Immunophenotyping data of the lymphoid and myeloid lineage are available upon request.
Antineo has developed models of secondary resistance to anti-PDL1 (ID MBT-2 anti-PDL1R). These  models have been developed in vivo without genetic modifications.  

 

Download PDF

Model characteristics

Organism
Mouse
Tissue of origin
Bladder
Pathology
Carcinoma
Model type
In vitro, Resistant, Syngeneic
Availability
Off the shelf (time of expansion)

Request this model

Tell us about your compound and your endpoints. Our team confirms feasibility, timelines and study design before any commitment.

Related models

Other models sharing the same tissue of origin.

Model
Organism
Tissue of origin
Pathology
Type
Human
Bladder
Carcinoma
XenograftIn vitro
Human
Bladder
Carcinoma
XenograftIn vitro
Human
Bladder
Grade II carcinoma
XenograftIn vitro
Human
Bladder
Squamous cell carcinoma
XenograftIn vitro

J82

Human
Bladder
Transitional cell carcinoma
XenograftIn vitro
Human
Bladder
Carcinoma
XenograftIn vitro