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PIONEERING CANCER RESEARCH
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Breast
BCM-15006
Model Details
Patient
PDX Model
Histology
Metastasis
Patient Treatment
Patient Information for Model: BCM-15006
Contact Model Developer
Model Contact
Model: BCM-15006
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-15006
Model Details - Initial Implantation of Patient Tissue
Biomarkers & Mutations
Model Details - Acceptable Conditions for Passaging
Mutations (Cancer Gene Census List)
Show/Hide Columns
The number of models in this collection with mutations in the listed gene;
may include models that are not publicly available for distribution.
The number of models in this collection with mutations at the listed site;
may include models that are not publicly available for distribution.
Total mutations showing: 48
F
P
1
2
3
4
N
E
Rows Per Page
10
15
25
50
Download
Gene
Filter by Gene
Chr
Filter by Chr
Start
End
Ref
Alt
cDNA Change
Codon Change
Protein Change
TVAF
Gene Mutation Freq.
Site Mutation Freq.
Most Severe Effect
All Effects
Mutation Impact
Transcript ID
ClinVar Clinical Significance
COSMIC ID
gnomAD Non-Cancer AF
dbSNP ID
Gene Mutation Freq.
Site Mutation Freq.
Transcript ID
ClinVar Clinical Significance
COSMIC ID
dbSNP ID
ACVR1
chr2
157765946
157765949
ATTC
A
c.1038_1040del
aaGAAt/aat
p.K346del
0.26
2
1
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000434821.7
2
1
ENST00000434821.7
AKAP9
chr7
92097327
92097330
TAGA
T
c.10373_10375del
AGA/-
p.R3458del
0.184
50
3
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000356239.8
rs757087367
50
3
ENST00000356239.8
rs757087367
ARID1A
chr1
26696849
26696849
G
A
c.446G>A
gGc/gAc
p.G149D
0.861
19
3
Missense Variant
Missense Variant
MODERATE
ENST00000324856.13
Uncertain_significance
COSV61376273
rs2080267760
19
3
ENST00000324856.13
Uncertain_significance
COSV61376273
rs2080267760
ATRX
chrX
77682471
77682471
C
G
c.2785G>C
Gag/Cag
p.E929Q
0.233
59
56
Missense Variant
Missense Variant
MODERATE
ENST00000373344.10
Benign
rs3088074
59
56
ENST00000373344.10
Benign
rs3088074
BARD1
chr2
214767531
214767532
CA
TG
c.1518_1519inv
caTGtg/caCAtg
p.V507M
0.486
34
24
Missense Variant
Missense Variant
MODERATE
ENST00000260947.9
COSV105837301
rs386654966
34
24
ENST00000260947.9
COSV105837301
rs386654966
BCR
chr22
23314599
23314599
C
G
c.3611C>G
gCc/gGc
p.A1204G
0.175
7
2
Missense Variant
Missense Variant
MODERATE
ENST00000305877.13
COSV59925974
0.000060068300
rs56265970
7
2
ENST00000305877.13
COSV59925974
rs56265970
BIRC6
chr2
32515477
32515480
ATTC
A
c.11059_11061del
aTTCtt/att
p.L3687del
0.211
15
3
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000421745.6
15
3
ENST00000421745.6
CDK12
chr17
39462615
39462618
GAGA
G
c.548_550del
gAGAag/gag
p.K183del
0.982
8
3
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000447079.6
8
3
ENST00000447079.6
CIC
chr19
42291340
42291340
C
T
c.2572C>T
Ccc/Tcc
p.P858S
0.97
11
3
Missense Variant
Missense Variant
MODERATE
ENST00000575354.6
COSV99360636
0.000175355000
rs139895527
11
3
ENST00000575354.6
COSV99360636
rs139895527
CIITA
chr16
10909070
10909070
A
G
c.2702A>G
cAg/cGg
p.Q901R
0.96
85
84
Missense Variant
Missense Variant
MODERATE
ENST00000618327.4
Benign
0.983235000000
rs7197779
85
84
ENST00000618327.4
Benign
rs7197779
CREB3L2
chr7
137928167
137928170
CTGG
C
c.299_301del
aCCAgt/agt
p.T100del
0.855
49
49
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000330387.11
COSV57791862
rs3217268
49
49
ENST00000330387.11
COSV57791862
rs3217268
ERBB3
chr12
56101214
56101214
A
T
c.3355A>T
Agc/Tgc
p.S1119C
0.95
14
9
Missense Variant
Missense Variant
MODERATE
ENST00000267101.8
Benign
COSV57247854
0.088057000000
rs773123
14
9
ENST00000267101.8
Benign
COSV57247854
rs773123
ERCC5
chr13
102846322
102846322
C
T
c.56C>T
cCc/cTc
p.P19L
0.954
14
3
Missense Variant
Missense Variant
MODERATE
ENST00000652225.2
Uncertain_significance
COSV99053842
0.000582552000
rs34291397
14
3
ENST00000652225.2
Uncertain_significance
COSV99053842
rs34291397
ERCC5
chr13
102862407
102862407
C
T
c.1258C>T
Cgt/Tgt
p.R420C
0.317
14
3
Missense Variant
Missense Variant
MODERATE
ENST00000652225.2
0.000012670500
rs374911899
14
3
ENST00000652225.2
rs374911899
FAM135B
chr8
138153029
138153030
TG
CA
c.1445_1446inv
cCA/cTG
p.P482L
0.657
35
29
Missense Variant
Missense Variant
MODERATE
ENST00000395297.6
rs71505459
35
29
ENST00000395297.6
rs71505459
Total mutations showing: 48
F
P
1
2
3
4
N
E
Rows Per Page
10
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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-15006
Patient
PDX
ER
H&E
HER2
PR
Metastasis Information for Model: BCM-15006
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-15006
Event Id
Treatment
Treatment Setting
Age at Start
Age at End
Duration
Clinical Response
Pathologic Response
Reason Stopped
20
Cyclophosphamide,Doxorubicin
Neoadjuvant
33.95
34.07
44 days
Partial Response
Not Reported
Treatment Completed
25
Carboplatin,Paclitaxel
Neoadjuvant
34.11
34.32
77 days
Progressive Disease
Not Reported
Treatment Completed
40
Radiation Therapy
Neoadjuvant
34.37
34.5
47 days
Complete Response
Pathological Complete Response
Treatment Completed
45
Cisplatin
Neoadjuvant
34.38
34.45
26 days
Complete Response
Pathological Complete Response
Treatment Completed
55
Capecitabine
Metastatic
34.78
35.28
183 days
Not Reported
Not Applicable
Treatment Completed
70
Radiation Therapy
Metastatic
35.78
35.85
26 days
Not Reported
Not Applicable
Treatment Completed
75
Capecitabine
Metastatic
35.8
35.92
44 days
Not Reported
Not Applicable
Disease Progression
80
Eribulin
Metastatic
35.93
35.94
4 days
Not Reported
Not Applicable
Disease Progression
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