PDX INSIGHTS
PIONEERING CANCER RESEARCH
Model Details

Patient Information for Model: BCM-15051

Model Contact
Model: BCM-15051
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-15051

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
ABL1chr9130884102130884105CAAGCc.1826_1828delAAG/-p.K609del0.0145542In-frame DeletionIn-frame DeletionMODERATEENST00000318560.6

COSV59324524
rs201725154
5542ENST00000318560.6COSV59324524rs201725154
AKAP9chr79200130692001306GTc.1389G>TatG/atTp.M463I0.99611573Missense VariantMissense VariantMODERATEENST00000356239.8
Benign
COSV62345589
0.376835000000rs6964587
11573ENST00000356239.8BenignCOSV62345589rs6964587
AKAP9chr79208559792085597CTc.8935C>TCct/Tctp.P2979S0.993115115Missense VariantMissense VariantMODERATEENST00000356239.8
Benign/Likely_benign
COSV104663065
0.996325000000rs1063242
115115ENST00000356239.8Benign/Likely_benignCOSV104663065rs1063242
AKAP9chr79208338492083384AGc.8375A>GaAt/aGtp.N2792S0.99611562Missense VariantMissense VariantMODERATEENST00000356239.8
Benign/Likely_benign
COSV62339152
0.357813000000rs6960867
11562ENST00000356239.8Benign/Likely_benignCOSV62339152rs6960867
AKAP9chr79202286492022864AAAACc.4004_4006dupaaa/aAACaap.K1335_L1336insQ0.99411573In-frame InsertionIn-frame InsertionMODERATEENST00000356239.8

COSV62337888
rs10644111
11573ENST00000356239.8COSV62337888rs10644111
ALKchr22992026229920262CTc.398G>AcGc/cAcp.R133H0.0078411151Missense VariantMissense VariantMODERATEENST00000389048.8
Uncertain_significance

0.000024843000rs768229646
1151ENST00000389048.8Uncertain_significancers768229646
ALKchr22919370629193706TCc.4381A>GAtc/Gtcp.I1461V0.999115115Missense VariantMissense VariantMODERATEENST00000389048.8
Benign
COSV101201052
0.997594000000rs1670283
115115ENST00000389048.8BenignCOSV101201052rs1670283
ANK1chr84170892041708920CTc.1856G>AcGt/cAtp.R619H0.9913711Missense VariantMissense VariantMODERATEENST00000289734.13
Benign/Likely_benign
COSV55882618
0.044445800000rs2304877
3711ENST00000289734.13Benign/Likely_benignCOSV55882618rs2304877
APCchr5112841059112841059TAc.5465T>AgTc/gAcp.V1822D0.99100100Missense VariantMissense VariantMODERATEENST00000257430.9
Benign
COSV57321643
0.794920000000rs459552
100100ENST00000257430.9BenignCOSV57321643rs459552
ARchrX6754531667545316TTGCAGCAc.234_239dupctg/ctGCAGCAgp.Q79_Q80dup0.08610115In-frame InsertionIn-frame InsertionMODERATEENST00000374690.9

COSV65953707
.
10115ENST00000374690.9COSV65953707.
ARchrX6754651467546514TTGGCc.1418_1420dup-/GGCp.G473dup0.93710118In-frame InsertionIn-frame InsertionMODERATEENST00000374690.9

COSV104687717
.
10118ENST00000374690.9COSV104687717.
ARchrX6754540067545403GGCAGc.271_273delagGCAg/aggp.Q91del0.01410124In-frame DeletionIn-frame DeletionMODERATEENST00000374690.9

COSV65954891
rs753526329
10124ENST00000374690.9COSV65954891rs753526329
ARchrX6754531667545316TTGCAGCAGCAc.231_239dupctg/ctGCAGCAGCAgp.Q78_Q80dup0.60910115In-frame InsertionIn-frame InsertionMODERATEENST00000374690.9

COSV105309998
.
10115ENST00000374690.9COSV105309998.
ARchrX6754531667545316TTGCAGCAGCAGCAc.228_239dupctg/ctGCAGCAGCAGCAgp.Q77_Q80dup0.2931018In-frame InsertionIn-frame InsertionMODERATEENST00000374690.9


.
1018ENST00000374690.9.
ARHGAP5chr143209213432092134GAc.1465G>AGag/Aagp.E489K0.044134Missense VariantMissense VariantMODERATEENST00000345122.8

COSV61533654
rs78337553
134ENST00000345122.8COSV61533654rs78337553
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-15051
Patient
PDX

Metastasis Information for Model: BCM-15051
 
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-15051

Event IdTreatmentTreatment SettingAge at StartAge at EndDurationClinical ResponsePathologic ResponseReason Stopped
10Carboplatin,PaclitaxelNeoadjuvant59.4559.6988 daysNot ReportedNo Response Treatment Completed
20Cyclophosphamide,DoxorubicinNeoadjuvant59.7659.815 daysProgressive DiseaseNot ApplicableDisease Progression
35Radiation Therapy Adjuvant59.9660.0844 daysNot ReportedNot ApplicableTreatment Completed
40CapecitabineAdjuvant60.0860.56175 daysNot ReportedNot ApplicableTreatment Completed













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