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. 2020 Jun 24;8(4):e00617. doi: 10.1002/prp2.617

TABLE 1.

Sensitivity to HER2‐targeted therapies and standard‐care chemotherapeutics

MDA‐MB‐361 S MDA‐MB‐361 TR MDA‐MB‐361 TCR
Drug target Drug name IC50 (nmol/L) IC50 (nmol/L) Relative resistance IC50 (nmol/L) Relative resistance
HER2 T‐DM1 0.23 1.95 7.9(***) 1.35 5.3(*)
Trastuzumab(#) 0.11 0.16 1.4 0.21 1.9
Pertuzumab 9.8 18.7 1.9 12.31 1.3
Lapatinib 4817 4428 0.9 3227 0.7
Afatinib 23.2 43.7 2.4(*) 13.1 0.6
Topoisomerase I Irinotecan 3443 5203 1.5 3797 1.1
PNU‐159682 0.10 0.16 1.0 0.1 0.8
DNA Antimetabolite Fluorouracil 16 227 9020 0.6 15 323 0.9
Alkylating Cisplatin 3867 7023 1.8 9457 2.4
Intercalating Doxorubicin 6.57 7.31 1.1 8.81 1.3
Tubulin Polymerizing Paclitaxel 0.08 0.17 2.0 0.23 2.7
Depolymerizing Vincristine 0.12 0.40 3.2 0.67 5.3(*)
Vinorelbine 2.26 3.99 2.8(*) 4.61 4.8
Colchicine 1.98 3.84 1.8(*) 2.27 1.5
S‐methylDM1 0.07 0.16 2.3 0.13 1.8
DM1 1.68 4.40 2.9(*) 3.52 4.7

The sensitivity after a 6 day exposure to the indicated anti‐cancer agents was studied by MTT cytotoxic assays. Data shown as the IC50 values of a single experiment, representative of 3‐4 independent experiments, and the relative resistance is the mean ratio of the IC50 of each resistant cell line over the parental cell line from 3‐4 independent experiments (#: IC75). Statistics were calculated using the Student t test (*:P < .05; **P < .01; ***P < .001).

Bold values indicate relative resistance numbers