PDX INSIGHTS
PIONEERING CANCER RESEARCH
Model Details

Patient Information for Model: BCM-15029

Model Contact
Model: BCM-15029
Model Contact: Michael Lewis
Institution: BCM Breast PDX Program
Email: mtlewis@bcm.edu

Patient Information
Clinical Timeline

Color Keys:
 
 Positive
 
 Negative
 
 N/A

Clinical Information at Collection
Clinical Biomarkers/Mutations at Collection
Pathology Information at Collection

Model Information for Model: BCM-15029

Model Details - Initial Implantation of Patient Tissue
Biomarkers & Mutations
Model Details - Acceptable Conditions for Passaging
Mutations (Cancer Gene Census List)

GeneChrStartEndRefAltcDNA ChangeCodon ChangeProtein ChangeTVAF Gene Mutation Freq. Site Mutation Freq.Most Severe EffectAll EffectsMutation ImpactTranscript IDClinVar Clinical SignificanceCOSMIC IDgnomAD Non-Cancer AFdbSNP IDGene Mutation Freq.Site Mutation Freq.Transcript IDClinVar Clinical SignificanceCOSMIC IDdbSNP ID
AKAP9chr79200130692001306GTc.1389G>TatG/atTp.M463I0.63811573Missense VariantMissense VariantMODERATEENST00000356239.8
Benign
COSV62345589
0.376835000000rs6964587
11573ENST00000356239.8BenignCOSV62345589rs6964587
AKAP9chr79208559792085597CTc.8935C>TCct/Tctp.P2979S0.986115115Missense VariantMissense VariantMODERATEENST00000356239.8
Benign/Likely_benign
COSV104663065
0.996325000000rs1063242
115115ENST00000356239.8Benign/Likely_benignCOSV104663065rs1063242
AKAP9chr79208338492083384AGc.8375A>GaAt/aGtp.N2792S0.73311562Missense VariantMissense VariantMODERATEENST00000356239.8
Benign/Likely_benign
COSV62339152
0.357813000000rs6960867
11562ENST00000356239.8Benign/Likely_benignCOSV62339152rs6960867
AKAP9chr79202286492022864AAAACc.4004_4006dupaaa/aAACaap.K1335_L1336insQ0.57911573In-frame InsertionIn-frame InsertionMODERATEENST00000356239.8

COSV62337888
rs10644111
11573ENST00000356239.8COSV62337888rs10644111
ALKchr22919350029193500GCc.4587C>GgaC/gaGp.D1529E0.60511580Missense VariantMissense VariantMODERATEENST00000389048.8
Benign
COSV66569695
0.472160000000rs1881421
11580ENST00000389048.8BenignCOSV66569695rs1881421
ALKchr22919370629193706TCc.4381A>GAtc/Gtcp.I1461V0.997115115Missense VariantMissense VariantMODERATEENST00000389048.8
Benign
COSV101201052
0.997594000000rs1670283
115115ENST00000389048.8BenignCOSV101201052rs1670283
ALKchr22919361529193615TCc.4472A>GaAg/aGgp.K1491R0.60311551Missense VariantMissense VariantMODERATEENST00000389048.8
Benign
COSV66555753
0.349007000000rs1881420
11551ENST00000389048.8BenignCOSV66555753rs1881420
APCchr5112828868112828869GTGc.1643delgTt/gtp.L548*0.4931001Frameshift MutationFrameshift MutationHIGHENST00000257430.9

COSV57325795
rs1554082091
1001ENST00000257430.9COSV57325795rs1554082091
APCchr5112841059112841059TAc.5465T>AgTc/gAcp.V1822D0.988100100Missense VariantMissense VariantMODERATEENST00000257430.9
Benign
COSV57321643
0.794920000000rs459552
100100ENST00000257430.9BenignCOSV57321643rs459552
ARchrX6754531667545319TGCATc.237_239delctGCAg/ctgp.Q80del0.51610135In-frame DeletionIn-frame DeletionMODERATEENST00000374690.9

COSV65954886
.
10135ENST00000374690.9COSV65954886.
ARchrX6754531667545325TGCAGCAGCATc.231_239delctGCAGCAGCAg/ctgp.Q78_Q80del0.44810116In-frame DeletionIn-frame DeletionMODERATEENST00000374690.9

COSV65958085
.
10116ENST00000374690.9COSV65958085.
ARHGEF10chr819293141929314TGc.2950T>GTcc/Gccp.S984A0.9714310Missense VariantMissense VariantMODERATEENST00000349830.8
Benign
COSV50664117
0.053800200000rs17683288
4310ENST00000349830.8BenignCOSV50664117rs17683288
ARID1Bchr6157190043157190043GCc.4064G>CaGt/aCtp.S1355T0.98804Missense VariantMissense VariantMODERATEENST00000636930.2

COSV104368469
.
804ENST00000636930.2COSV104368469.
ATICchr2215325297215325297CGc.347C>GaCt/aGtp.T116S0.9855243Missense VariantMissense VariantMODERATEENST00000236959.14
Benign
COSV52691660
0.326476000000rs2372536
5243ENST00000236959.14BenignCOSV52691660rs2372536
ATRchr3142459302142459302CTc.7274G>AcGa/cAap.R2425Q0.23310124Missense VariantMissense VariantMODERATEENST00000350721.9
Benign
COSV63383988
0.130080000000rs2229032
10124ENST00000350721.9BenignCOSV63383988rs2229032
CNV

PDX Validation
In order to validate the identity of Baylor College of Medicine patient-derived xenograft (PDX) models, short tandem repeat (STR) testing is performed at the Cytogenetics and Cell Authentication core facility at MDACC. STR testing is performed on tissue from the initial tumor grown in the mouse (transplant generation 1 - TG1) and from a patient sample when possible. Thereafter, STR testing is performed every five transplant generations (TG5, TG10, TG15, and TG20). In the case that a PDX model is transplanted from viably frozen tissue to restart the model, the PDX Core will test the first outgrowth to confirm identity and every five transplant generations thereafter. In addition to STR, we assess clinical biomarkers and histology every 5th transplant generation. Finally, RNAseq gene expression profiles are evaluated periodically to ensure consistency with previous results and to evaluate phenotypic drift. If a significant change in PDX biology is noted, we identify the last known stable stock and re-start the model.

Histology Information for Model: BCM-15029
Patient
PDX

Metastasis Information for Model: BCM-15029
 
Patient
PDX
Abdomen
Adrenal gland
Bone
Bones
Brain
CTC
Chest
Chest wall
Contralateral Breast
Dura
Fallopian Tubes
Head
Kidney
Liver
Lung
Lymph node
Lymph nodes
Neck
Ovary
Pancreas
Pericardium
Peritoneal cavity
Peritoneum
Pleura
Pleural effusion
Shoulder
Skin
Spine
Spleen
Thoracic Spine
Thymus

Patient Treatment Information for Model: BCM-15029

Event IdTreatmentTreatment SettingAge at StartAge at EndDurationClinical ResponsePathologic ResponseReason Stopped
10Cyclophosphamide,Doxorubicin,Radiation TherapyAdjuvant46.8947.56245 daysNot ReportedNot ReportedTreatment Completed
30Carboplatin,DocetaxelNeoadjuvant63.0563.2884 daysPartial ResponsePartial ResponseSide Effects













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