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

Sarcoma

 

Table I : cell lines with wt p53

Cell line
ATCC
 
Reference
FPBH   Ewing sarcoma  
SAL-2   Ewing sarcoma  
STA-ET-1   Ewing sarcoma  
WE-68   Ewing sarcoma  
VH-64   Ewing sarcoma  
STA-ET-6   Ewing sarcoma  
TC 252   Ewing sarcoma  
       
U2OS* HTB-96 Osteosarcoma  
SJSA** CRL-2098 Osteosarcoma  
       
HT1080 CCL-121 Fibosarcoma  
       
A-204   Undifferentiated sarcoma  
       

           

* Mdm2 overexpression
**Mdm2 amplification

Table II : cell lines with p53 gene deletion or rearrangement

Cell line
ATCC
 
Reference
Saos-2 HTB-85 Osteosarcoma  
SK-N-MC HTB-10 Ewing sarcoma  

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
Angiosarcoma (hepatic)
179 CAT CTT His Leu SM ASL5 38 1353 Single report
Chondrosarcoma
175 CGC CAC Arg His SM CH-1 1187 1373 Single report
Ewing's Sarcoma
194 CTT CGT Leu Arg SM 19 66 328 Single report
175 CGC CAC Arg His SM 58 1187 328 Single report
176 TGC TTC Cys Phe SM 59 191 328 Single report
273 CGT TGT Arg Cys SM 63 687 328 Single report
285 GAG AAG Glu Lys SM 64 165 328 Single report
118 ACA ins2 Thr Fs. SM A673 1 226 wt in COSMIC
283 CGC DEL1C Arg Fs. SM ES-1-OT 4 245 Single report
181 CGC CAC Arg His SM EW-13 34 2249 Mutation in COSMIC database
164 AAG GAG Lys Glu SM EW-24 25 2249 Mutation in COSMIC database
273 CGT TGT Arg Cys SM IARC-EW2 687 226 Single report
273 CGT TGT Arg Cys SM RD-ES 687 226 Confirmed in another publication
273 CGT CAT Arg His SM RM 82 780 226 Single report
176 TGC TTC Cys Phe SM SCMC-ES-2 191 245 Single report
141 TGC TAC Cys Tyr SM SCMCS-ES-1 103 245 Single report
176 TGC TTC Cys Phe SM SK-ES-1 191 226 Confirmed in another publication
176 TGC TTC Cys Phe SM SK-PN-DW 191 2249 Mutation in COSMIC database
273 CGT TGT Arg Cys SM SMB 687 226 Single report
277 TGT TAT Cys Tyr SM STA-ET-2.1 28 226 Single report
273 CGT TGT Arg Cys SM STA-ET-7.1 687 226 Single report
176 TGC TTC Cys Phe SM W-ES 191 245 Single report
Fibrosarcoma
213 CGA TGA Arg Stop SM SW684 306 2249 Mutation in COSMIC database
Leyomyosarcoma
215 AGT ins1 Ser Fs. SM LMS6-93 3 1552 Single report
237 ATG AAG Met Lys DMU SK-LMS-1 11 2198 Controversy with other publications
245 GGC AGC Gly Ser SM SK-LMS-1 440 14 Controversy with other publications
245 GGC AGC Gly Ser DMU SK-LMS-1 440 2198 Controversy with other publications
175 CGC CAC Arg His DMU SK-UT-1 1187 2249 Controversy with other publications
175 CGC CAC Arg His SM SK-UT-1 1187 14 Controversy with other publications
248 CGG CAG Arg Gln DMU SK-UT-1 883 2249 Controversy with other publications
Liposarcoma
251 ATC AAC Ile Asn SM SW872 21 2249 Mutation in COSMIC database
Osteosarcoma
156 CGC CCC Arg Pro SM HOS 38 25 Confirmed in another publication
306 CGA TGA Arg Stop SM HOSM-2 160 1920 Single report
76 GCA ins1a Ala Fs. SM HuO-3N1 1 2249 Mutation in COSMIC database
286 GAA AAA Glu Lys SM OH 86 272 Single report
250 CCC del8 Pro Fs. SM RIT-1B 1 65 Single report
245 GGC AGC Gly Ser SM RIT2 440 65 Single report
Rhabdomyosarcoma
219 CCC del4 Pro Fs. SM ctr 1 97 Single report
248 CGG TGG Arg Trp SM RD 728 14 Confirmed in another publication. wt in COSMIC
273 CGT TGT Arg Cys SM Rh30 687 1190 Controversy with other publications
280 AGA AGT Arg Ser SM RH30 14 97 Controversy with other publications
156 CGC CCC Arg Pro SM RMS 38 14 Single report
Sarcoma
316 CCC CCT Pro Pro SM GCT 6 2249 Mutation in COSMIC database
317 CAG TAG Gln Stop SM GCT 25 2249 Mutation in COSMIC database
326 GAA TAA Glu Stop SM S-117 9 2249 Mutation in COSMIC database

 

 

 
 
Home | Our Work |p53 Info| p53 Database | p53 Link | Contact us