Table 1.
Cancer type | Cell line/PDX | Name | BRAF | TP53 |
---|---|---|---|---|
PTC | Cell line | TPC-1 | WT | WT |
Cell line | K2 | V600E | WT | |
Cell line | BCPAP | V600E | D259Y | |
Cell line | MDA-T85 | V600E | WT | |
PDTC | Cell line | MDA-T192 | WT | WT |
ATC | Cell line | MDA-T178 | WT | WT |
Cell line | U-Hth83 | WT | Y236C and P153fs | |
Cell line | Hth7 | WT | G245S | |
Cell line | MDA-T187 | V600E | K132N | |
Cell line | SW1736 | V600E | No expression, Q192a | |
Cell line | Hth104 | V600E | No expression | |
Cell line | 8505C | V600E | R248G | |
PDX | MDA-ATC1 | V600E | K132N | |
PDX | MDA-ATC5 | WT | WT |
The mutation status of BRAF and TP53 was determined by whole exome sequencing, Sequenom, or Sanger sequencing. The expression of TP53 in Hth104 cells was determined by Western blot analysis after failed Sanger sequencing. MDA-ATC1 was generated from the same patient who gave rise to MDA-T187 cell line and carrying the same BRAF and TP53 mutations as determined by whole-exome sequencing.
Abbreviations: ATC, anaplastic thyroid carcinoma; PDTC, poorly differentiated thyroid carcinoma, PDX, patient-derived xenograft; PTC, papillary thyroid carcinoma; WT, wild-type.
a Nonsense mutation.