Cell lines database

p53 database

p53 mutations in cell lines

The hanbook of p53 mutation in cell lines

Cell lines with a controversial p53 status

The NCI 60 panel

Bladder cancer cell lines

Brain cancer cell lines

Breast cancer cell lines

Cervical carcinoma

Colorectal cancer cell lines

Esophageal cancer cell lines

Gastric cancer cell lines

Head and Neck cancer cell lines

Leukemia / Lymphoma cell lines

NSCLC cancer cell lines

Ovarian cancer cell lines

Pancreatic cancer cell lines

Sarcoma cell lines

SCLC cancer cell lines

Melanoma cell lines

Hepatocellular carcinoma

References

Breast carcinoma

Table I : cell lines with wt p53

Cell line ATCC
Reference
MCF-7 HTB-22
2091
MCF10-2A  
DU4475 HTB-123
2091
MDA-MB-175VII HTB-25
2091
MPE600  
2091
SK-BR-7  
2091
SUM102PT  
2091
UACC-812 CRL-1897
2091
ZR75-1 CRL-1500
2091
ZR75-30 CRL-1504
2091
HBL-100*  
2029
MRK-NU-1  
1006
YMB-1  
1006
YMB-1-E  
1006

*Positive for SV40

Table II : cell lines with p53 gene deletion or rearrangement

Cell line ATCC Reference
MDA- MB-157 HTB-24  

Table III : cell lines with p53 splice mutation
(exonic mutations that modify splice are listed in table IV)

no data

Table IV: cell lines with p53 mutations (missense or frameshift)
More information is available in the handbook

Pos: Codon position (1 to 393);
WT: Normal base sequence of the codon in which the mutation occurred;
Mut Sequence of the mutated codon. If the mutation is a deletion or an insertion, it is indicated by "del" or "ins" followed by the number of deleted or inserted bases. The position in the codon is indicated by “a”, “b”, or “c” for the first, second or third base of the codon respectively. Example: "del66b" is a deletion of 66 bases including the second base of the codon; "ins4a" is an insertion of 4 bases occurring between the first and the second base of the codon. Label a, b, or c is omitted if the boundary of the deletion or insertion is unknown
AA: Wild type amino acid;
Mut: Mutant amino acid. Stop: nonsense mutation: Fs.: Frameshift mutation: InF: In-frame insertion or deletion;
Comp: complexity of the mutation: SM: Single mutational event in the tumor; DMU (Double Mutation Unknown): Two p53 mutations in the same tumor but their allelique distribution is unknown; DMD (Double Mutation Different allele): Two p53 mutations in the same tumor on two different p53 alleles; DMS (Double Mutation Same allele): Two p53 mutations in the same tumor on the same p53 allele: MM (Multiple Mutation): More than two p53 mutations in the same tumor;
NB: Number of tumors with this particular mutant in the database;
Ref: reference number;
Comments: information;

Table of references (available also in the handbook)

Pos.
WT
Mut
      AA
Mut
Comp
Name
NB
Ref
Comments
179 CAT AAT His Asn SM 3522 S2 23 1017 Single report
266 GGA TGA Gly Stop SM BRC-230 19 1393 Single report
132 AAG CAG Lys Gln SM BT-20 14 24 Confirmed in another publication. wt in COSMIC
285 GAG AAG Glu Lys SM BT-474 165 24 Confirmed in three other publications
246 ATG del1c Met Fs. SM BT-483 1 2029 Controversy with other publications
246 ATG ATA Met Ile SM BT-483 33 2091 Controversy with other publications
249 AGG AGC Arg Ser SM BT-549 34 24 Single report
224 GAG AAG Glu Lys SM CAL-148 8 2249 Mutation in COSMIC database
132 AAG GAG Lys Glu SM CAL-85-1 25 2249 Mutation in COSMIC database
280 AGA ACA Arg Thr SM CAMA-1 92 2029 wt in COSMIC
241 TCC TGC Ser Cys SM EVSA-T 36 2091 wt in COSMIC
248 CGG CAG Arg Gln SM H-31 883 1689 Single report
262 GGT GTT Gly Val SM H-71 14 1689 Single report
281 GAC CAC Asp His SM HCC1007 41 1396 Single report
281 GAC TAC Asp Tyr SM HCC1008 16 2258  
248 CGG CAG Arg Gln SM HCC1143 883 2249 Mutation in COSMIC database
248 CGG CAG Arg Gln SM HCC1143 883 2258  
108 GGT del3b Gly InF SM HCC1187 1 2258  
108 GGT del3a Gly InF SM HCC1187 1 2249 Mutation in COSMIC database
175 CGC CAC Arg His SM HCC1395 1187 1396 Single report
175 CGC CAC Arg His SM HCC1395 1187 2258  
74 GCC del6a Ala InF DMU HCC1419 1 2249 Mutation in COSMIC database
220 TAT TGT Tyr Cys DMU HCC1419 336 2249 Mutation in COSMIC database
294 GAG TAG Glu Stop SM HCC1569 54 1396 Single report
256 ACA ins2 Thr Fs. SM HCC1806 2 1396 Single report
306 CGA TGA Arg Stop SM HCC1937 160 1396 Confirmed in another publication
306 CGA TGA Arg Stop SM HCC1937 160 2258  
163 TAC TGC Tyr Cys SM HCC1954 140 2258  
163 TAC TGC Tyr Cys SM HCC1954 140 2249 Mutation in COSMIC database
248 CGG TGG Arg Trp SM HCC2157 728 2249 Mutation in COSMIC database
248 CGG TGG Arg Trp SM HCC2157 728 2258  
283 CGC TGC Arg Cys SM HCC2218 27 1396 Single report
241 TCC del1b Ser Fs. SM HCC2713 26 2258  
213 CGA TGA Arg Stop SM HCC2998 306 2249 Mutation in COSMIC database
273 CGT CTT Arg Leu SM HCC38 147 1396 Single report
273 CGT CTT Arg Leu SM HCC38 147 2258  
248 CGG CAG Arg Gln SM HCC70 883 1396 Single report
213 CGA TGA Arg Stop SM HDQ-P1 306 1713 Single report
249 AGG GGG Arg Gly SM HMT-3909 52 552 Single report
157 GTC TTC Val Phe SM Hs 578T 177 76 Confirmed in two other publications
157 GTC TTC Val Phe SM HS578T 177 2258  
215 AGT ATT Ser Ile SM L56BR-X1 25 1968 Single report
244 GGC AGC Gly Ser SM MAST 72 1393 Single report
285 GAG AAG Glu Lys SM MDA-MB-134-VI 165 2029 wt in COSMIC
261 AGT del26a Ser Fs. SM MDA-MB-157 1 2029 wt in COSMIC
280 AGA AAA Arg Lys SM MDA-MB-231 78 24 Confirmed in another publication
220 TAT TGT Tyr Cys SM MDA-MB-330 336 2091 Single report
166 TCA TAA Ser Stop SM MDA-MB-361 19 2029 wt in COSMIC
236 TAC TGC Tyr Cys SM MDA-MB-415 75 2091 Single report
266 GGA GAA Gly Glu SM MDA-MB-435 74 1018 Single report
204 GAG ins7c Glu Fs. SM MDA-MB-436 1 2029 Controversy with other publications
273 CGT CAT Arg His SM MDA-MB-436 780 1367 Controversy with other publications
368 CAC del30 His InF SM MDA-MB-453 1 147 wt in COSMIC
273 CGT CAT Arg His SM MDA-MB-468 780 9 Confirmed in another publication
132 AAG AGG Lys Arg SM MFM-223 51 2249 Mutation in COSMIC database
234 TAC TAA Tyr Stop SM MW1C-6.3 10 147 Single report
244 GGC AGC Gly Ser SM OCUB-F 72 2091 Single report
244 GGC AGC Gly Ser SM OCUB-M 72 2249 Mutation in COSMIC database
277 TGT TTT Cys Phe SM R11T 48 1806 Single report
136 CAA TAA Gln Stop SM R18T 47 1806 Single report
273 CGT TGT Arg Cys SM R30T 687 1806 Single report
175 CGC CAC Arg His SM SK-BR-3 1187 76 Confirmed in another publication. wt in COSMIC
161 GCC GAC Ala Asp SM SK-BR-5 19 2091 Single report
135 TGC TTC Cys Phe SM SUM1315MO2 52 2091 Single report
237 ATG ATA Met Ile SM SUM149PT 123 2091 Single report
158 CGC ins3a Arg InF SM SUM159PT 1 2091 Single report
144 CAG TAG Gln Stop SM SUM185PE 53 2091 Single report
317 CAG TAG Gln Stop SM SUM190PT 25 2091 Single report
265 CTG CCG Leu Pro SM SUM225CWN 23 2091 Single report
273 CGT TGT Arg Cys SM SUM229PE 687 2091 Single report
213 CGA TGA Arg Stop SM SUM52PE 306 2091 Single report
194 CTT TTT Leu Phe SM T47D 28 9 Confirmed in another publication
342 CGA TGA Arg Stop SM UACC-893 74 2029 Single report

 

 

 

 

 
 
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