General Information of This Antibody-drug Conjugate (ADC)
ADC ID
DRG0HYAKW
ADC Name
WT ADC
Synonyms
WT ADC
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Organization
The State University of New York at Buffalo.
Drug Status
Investigative
Structure
Antibody Name
Trastuzumab
 Antibody Info 
Antigen Name
Receptor tyrosine-protein kinase erbB-2 (ERBB2)
 Antigen Info 
Payload Name
Monomethyl auristatin E
 Payload Info 
Therapeutic Target
Microtubule (MT)
 Target Info 
Linker Name
Mc-Val-Cit-PABC
 Linker Info 
Conjugate Type
Site specific conjugation at LC-V205C.
Combination Type
Vedotin
General Information of The Activity Data Related to This ADC
Revealed Based on the Cell Line Data
Click To Hide/Show 3 Activity Data Related to This Level
Standard Type Value Units Cell Line Disease Model
Half Maximal inhibitory Concentration (lC50) 
0.2
nM
CVCL_1603
Gastric tubular adenocarcinoma
Half Maximal inhibitory Concentration (lC50) 
296
nM
CVCL_0419
Breast adenocarcinoma
Half Maximal inhibitory Concentration (lC50) 
1603
nM
CVCL_0031
Invasive breast carcinoma
Full List of Activity Data of This Antibody-drug Conjugate
Revealed Based on the Cell Line Data
Click To Hide/Show 3 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal inhibitory Concentration (lC50) 0.2 nM High HER2 expression (HER2 +++)
Method Description
The MTT (3- (4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assays were performed using WT ADC and positively charged ADC in three cell lines with varying HER2 expression levels: N87 (high), MCF-7 (low), and MDA-MB-468 (non-expressing). Cells were seeded at a density of 10,000 cells per well in 96-well plates and incubated for 24 h before treatment. ADCs were added at concentrations ranging from 0.01 nM to 1000 nM, and cells were incubated for an additional 96 h. Following treatment, 5 mg/mL MTT solution was added to each well and incubated for 4 h, after which 10% SDS-HCl solution was added to dissolve the formazan crystals. Absorbance was measured at 570 nm the next day. Cell viability (%) was calculated as (ODtreated/ (ODcontrol) × 100%. GraphPad Prism (version 10.4.1) was used for curve fitting of the sigmoidal dose-response curves (cell viability vs. ADC concentration) under the nonlinear regression option, and the half-maximal inhibitory concentration (IC50) values were determined.

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In Vitro Model Gastric tubular adenocarcinoma NCI-N87 cells CVCL_1603
Experiment 2 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal inhibitory Concentration (lC50) 296 nM Negative HER2 expression (HER2-)
Method Description
The MTT (3- (4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assays were performed using WT ADC and positively charged ADC in three cell lines with varying HER2 expression levels: N87 (high), MCF-7 (low), and MDA-MB-468 (non-expressing). Cells were seeded at a density of 10,000 cells per well in 96-well plates and incubated for 24 h before treatment. ADCs were added at concentrations ranging from 0.01 nM to 1000 nM, and cells were incubated for an additional 96 h. Following treatment, 5 mg/mL MTT solution was added to each well and incubated for 4 h, after which 10% SDS-HCl solution was added to dissolve the formazan crystals. Absorbance was measured at 570 nm the next day. Cell viability (%) was calculated as (ODtreated/ (ODcontrol) × 100%. GraphPad Prism (version 10.4.1) was used for curve fitting of the sigmoidal dose-response curves (cell viability vs. ADC concentration) under the nonlinear regression option, and the half-maximal inhibitory concentration (IC50) values were determined.

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In Vitro Model Breast adenocarcinoma MDA-MB-468 cells CVCL_0419
Experiment 3 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal inhibitory Concentration (lC50) 1603 nM Low HER2 expression (HER2+)
Method Description
The MTT (3- (4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assays were performed using WT ADC and positively charged ADC in three cell lines with varying HER2 expression levels: N87 (high), MCF-7 (low), and MDA-MB-468 (non-expressing). Cells were seeded at a density of 10,000 cells per well in 96-well plates and incubated for 24 h before treatment. ADCs were added at concentrations ranging from 0.01 nM to 1000 nM, and cells were incubated for an additional 96 h. Following treatment, 5 mg/mL MTT solution was added to each well and incubated for 4 h, after which 10% SDS-HCl solution was added to dissolve the formazan crystals. Absorbance was measured at 570 nm the next day. Cell viability (%) was calculated as (ODtreated/ (ODcontrol) × 100%. GraphPad Prism (version 10.4.1) was used for curve fitting of the sigmoidal dose-response curves (cell viability vs. ADC concentration) under the nonlinear regression option, and the half-maximal inhibitory concentration (IC50) values were determined.

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In Vitro Model Invasive breast carcinoma MCF-7 cells CVCL_0031
References
Ref 1 PK/PD of Positively Charged ADC in Mice