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Table 1 Characterization of oncogenic alterations in melanoma cell lines tested for sensitivity to TAK733

From: Antitumor effects of the investigational selective MEK inhibitor TAK733 against cutaneous and uveal melanoma cell lines

Driver Oncogenic Mutation

Cell Line

Known Oncogenic Alterations

Wild type for BRAF and NRAS

M230

KIT L576P

M257

CDKN2A R80

BRAF amplification

M285

None detected

M368

None detected

M375

None detected

NRAS Mutants

M202

NRAS Q61L

EGFR amplification

CDKN2A homozygous deletion

M207

NRAS Q61L

MITF amplification

EGFR L747_P753 > S

PTEN heterozygous deletion

M243

NRASQ61H homozygous

PTENE156G heterozygous

CTNNB1_D32Y

M245

NRASQ61K heterozygous

TP53 R273H

M244

NRASQ61K heterozygous

M296

NRASQ61R heterozygous

M318

NRASQ61L heterozygous

PIK3CA C420R

SBCL2

NRASQ61K homozygous

Wn1366

NRASQ61L heterozygous

BRAF mutants

M229

BRAFV600E homozygous

BRAF amplification

MITF amplification

AKT1 amplification

PTEN heterozygous deletion

M233

BRAFV600E heterozygous

BRAF amplification

AKT1 amplification

CCND1 amplification

EGFR amplification

CDKN2A homozygous deletion

PTEN homozygous deletion

M238

BRAFV600E heterozygous1

CDKN2A homozygous deletion

PTEN heterozygous deletion

M249

BRAFV600E heterozygous

BRAF amplification

MITF amplification

AKT2 amplification

PTEN homozygous deletion

M255

BRAFV600E heterozygous

AKT2 amplification

CCND1 amplification

EGFR amplification

CDKN2A homozygous deletion

M262

BRAFV600E homozygous

AKT1 E17K

AKT1 amplification

EGFR amplification

CDKN2A homozygous deletion

M263

BRAFV600E heterozygous

CDKN2A heterozygous deletion

M275

BRAFV600E heterozygous

M297

BRAFV600E homozygous

PTENG165X homozygous

M299

BRAFV600E heterozygous

M308

BRAFV600E heterozygous

BRAF amplification

MITF amplification

AKT2 amplification

EGFR amplification

CDKN2A heterozygous deletion

SKmel28

BRAFV600E homozygous

EGFR P753S

MITF amplification

CCND1 amplification

CDKN2A heterozygous deletion

PTEN heterozygous deletion

GNAQ or GNA11

Mel20-06-039

GNAQQ209L heterozygous

 

Mel20-06-045

GNAQQ209P heterozygous

 

Mel20-07-070

GNA11Q209L heterozygous

 

Mel20-08-128

GNA11Q209L heterozygous

 

Mel20-09-196

GNAQQ209P heterozygous

  1. Legend: 1Tandem mutation where the codon changed from GTG to GAA.