Table 1.
Summary of molecular and cytogenetic data for 18q21.1 status in colorectal cancer cell lines
Cell line | MSI* | B8 Western† | SMAD4 mutation‡ | Predicted effect of mutation§ | Loss at SMAD4¶ | Loss at DCC∥ | Karyotype** | 18q21 status‡‡ | TGFBIIR†† |
---|---|---|---|---|---|---|---|---|---|
COLO678 | MSI− | Absent | EX1 − 11del | No protein | Yes | Yes | ? | — | |
COLO201 | MSI− | Absent | EX1 − 4del | No protein | Yes | Yes | 78 | 2 copies | None |
COLO205 | MSI− | Absent | EX1 − 4del | No protein | Yes | Yes | 68 | 2 copies | None |
VACO10 | MSI− | Absent | c.715C>T (Q239X), EX5 | Nonsense | Yes | Yes | 115 | — | None |
C10 | MSI− | Absent | IVS6 − 1G>T | Splice disruption | Yes | Yes | 49 | — | — |
HT29/CX1 | MSI− | Absent | c.931C>T (Q311X), EX7 | Nonsense | 2/3 markers | Yes | 71 | 2 copies | None |
SW480 | MSI− | Absent | IVS7 + 5G>C | Splice disruption | Yes | Yes | 57 | 1 copy | None |
SW620 | MSI− | Absent | IVS7 + 5G>C | Splice disruption | Yes | Yes | 50 | 1 copy | None |
CACO2 | MSI− | Present | c.1051G>C (D351H), EX8 | Missense | Yes | Yes | 96 | — | None |
C80 | MSI− | Present | c.1051G>C (D351H), EX8 | Missense | Yes | Yes | 69 | 2 copies | — |
SW403 | MSI− | Absent | EX10 − 11del | Truncated protein | Yes | Yes | 68 | 2 copies | — |
SW948 | MSI− | Present | c.1609G>T (D537Y), EX11 | Missense | Yes | No | 67 | — | — |
SW1222 | MSI− | Present | c.1619T>G (L540R), EX11 | Missense | Yes | Yes | ? | 18q loss | — |
SW1116 | MSI− | Absent | None found | Yes | Yes | 63 | — | — | |
HT55 | MSI− | Absent | None found | Yes | Yes | 80 | 2 copies | — | |
C106 | MSI− | Absent | None found | Yes | Yes | 79 | 2 copies | — | |
PC/JW | MSI− | Absent | None found | Yes | Yes | 70 | 2 copies | — | |
SW1417 | MSI− | Absent | None found | Yes | No | 70 | 2 copies | — | |
SW837 | MSI− | Present | None found | Yes | Yes | 40 | 1 copy | None | |
C99 | MSI− | Present | None found | Yes | Yes | 52 | 1 copy | — | |
C84 | MSI− | Present | None found | No | Yes | 56 | 1 copy | — | |
C125 | MSI− | Present | None found | Yes | Yes | 60 | 1 copy | — | |
VACO4A | MSI− | Present | None found | Yes | Yes | 60 | 2 copies | — | |
HCA46 | MSI− | Present | None found | Yes | Yes | 71 | 2 copies | None | |
C32 | MSI− | Present | None found | Yes | Yes | 74 | 2 copies | — | |
LIM21-1863 | MSI− | Present | None found | Yes | Yes | 80 | 3 copies | — | |
C70 | MSI− | Present | None found | Yes | Yes | 127 | 4 copies | — | |
COLO320 | MSI− | Present | None found | Yes | Yes | 53 | — | None | |
VACO4S | MSI− | Present | None found | Yes | Yes | 64 | — | — | |
LS1034 | MSI− | Present | None found | Yes | Yes | 77 | — | — | |
HRA19 | MSI− | Present | None found | Yes | Yes | ? | — | — | |
SKC01 | MSI− | Present | None found | No | Yes | hypertriploid | — | — | |
HCT8 | MSI+ | Present | None found | No | No | ? | — | — | |
LS180 | MSI+ | Present | None found | No | No | 45 | — | — | |
SW48 | MSI+ | Present | None found | No | No | 47 | — | Mutant × 2 | |
LS174T | MSI+ | Present | None found | No | No | 45 | 2 copies | Mutant × 2 | |
DLD1/HCT15 | MSI+ | Present | None found | No | No | 46 | 2 copies | Mutant × 2 | |
LOVO | MSI+ | Present | None found | No | No | 49 | 2 copies | Mutant × 2 | |
VACO5 | MSI+ | Present | None found | No | No | 47 | 2 copies | Mutant × 2 | |
HCA7 | MSI+ | Present | None found | No | No | 43 | 2 copies | Mutant × 2 | |
HCT116 | MSI+ | Present | None found | No | No | 45 | 2 copies | Mutant × 2 | |
LS411 | MSI+ | Present | None found | No | No | 75 | 2 copies | Mutant × ? | |
GP2D | MSI+ | Present | None found | No | No | 46 | 2 copies | — | |
COLO741 | MSI+ | Present | None found | Yes | Yes | ? | 2 copies | — |
COLO201/COLO205, HT29/CX1, and DLD1/HCT8/HCT15 are essentially identical cell lines.
MSI status.
SMAD4 protein expression as assessed by using B8 and western blotting.
Identified SMAD4 mutations.
Predicted effect of SMAD4 mutations.
∥ Allelic loss as inferred from homozygosity at microsatellite markers near SMAD4 and at DCC, respectively.
Modal chromosome number of cell line (?, not known).
18q21.1 status as determined by CGH, SKY, and FISH (—, not done).
TGFBIIR mutation status (—, not done).