Panc 04.03Homo sapiens (Human)Cancer cell line

Also known as: PL 5, PL-5, PL5, Pa017C, Pa17C, PANC403, Panc0403, PANC0403, Panc4.03, PANC 4.03, Panc 4.03, Panc04.03, Panc_04_03, PANC-04-03

🤖 AI SummaryBased on 10 publications

Quick Overview

Pancreatic cancer cell line with known chromosomal abnormalities and genetic mutations.

Detailed Summary

Panc 04.03 is a human pancreatic cancer cell line derived from a primary tumor. It exhibits complex chromosomal abnormalities, including gains and losses of specific chromosomes, which are common in pancreatic ductal adenocarcinoma. This cell line has been used in studies to investigate the molecular mechanisms of pancreatic cancer, including the role of specific genes such as DPC4/SMAD4 and their impact on drug sensitivity. Research has shown that Panc 04.03 is sensitive to certain chemotherapeutic agents, and its genetic profile has been characterized in multiple studies, providing insights into the genetic basis of pancreatic cancer progression and treatment response.

Research Applications

Molecular cytogenetic analysisDrug sensitivity profilingGenetic mutation analysisMetabolic profilingImmunotherapy research

Key Characteristics

Chromosomal abnormalitiesDPC4/SMAD4 inactivationSensitivity to chemotherapeutic agentsGenomic instability
Generated on 6/17/2025

Basic Information

Database IDCVCL_1636
SpeciesHomo sapiens (Human)
Tissue SourcePancreas[UBERON:UBERON_0001264]

Donor Information

Age70
Age CategoryAdult
SexMale
Racecaucasian

Disease Information

DiseasePancreatic ductal adenocarcinoma
LineagePancreas
SubtypePancreatic Adenocarcinoma
OncoTree CodePAAD

DepMap Information

Source TypeATCC
Source IDACH-000235_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Gly245Ser (c.733G>A)UnspecifiedSomatic mutation acquired during proliferationPubMed=28445466
MutationSimpleKRASp.Gly12Asp (c.35G>A)Unspecified-PubMed=29786757
MutationSimpleAPCp.Thr1556fs*3 (c.4660_4661insA) (E1554fs)Heterozygous-from parent cell line Panc 04.03
Gene fusionATG7ATG7-RAF1--from parent cell line Panc 04.03

Haplotype Information (STR Profile)

Short Tandem Repeat (STR) profile for cell line authentication.

Amelogenin
X
CSF1PO
12
D13S317
11,12
D16S539
11,12
D18S51
15,16
D19S433
15
D21S11
28
D2S1338
18,19
D3S1358
15,17
D5S818
11
D7S820
8,12
D8S1179
10,15
FGA
22,23
Penta D
10,13
Penta E
13,14
TH01
9.3
TPOX
10,11
vWA
14,16
Gene Expression Profile
Gene expression levels and statistical distribution
Loading cohorts...
Full DepMap dataset with combined data across cell lines

Loading gene expression data...

Publications

Pan-cancer proteomic map of 949 human cell lines.";

Robinson P.J., Zhong Q., Garnett M.J., Reddel R.R.

Cancer Cell 40:835-849.e8(2022).

Quantitative proteomics of the Cancer Cell Line Encyclopedia.";

Sellers W.R., Gygi S.P.

Cell 180:387-402.e16(2020).

Next-generation characterization of the Cancer Cell Line Encyclopedia.

Sellers W.R.

Nature 569:503-508(2019).

Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.

Stronach E.A., Saez-Rodriguez J., Yusa K., Garnett M.J.

Nature 568:511-516(2019).

An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.

Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.

Cancer Res. 79:1263-1273(2019).

Differential effector engagement by oncogenic KRAS.";

McCormick F.

Cell Rep. 22:1889-1902(2018).

Characterization of human cancer cell lines by reverse-phase protein arrays.

Liang H.

Cancer Cell 31:225-239(2017).

A landscape of pharmacogenomic interactions in cancer.";

Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.

Cell 166:740-754(2016).

Resolution of novel pancreatic ductal adenocarcinoma subtypes by global phosphotyrosine profiling.

Biankin A.V., Wu J.-M., Daly R.J.

Mol. Cell. Proteomics 15:2671-2685(2016).

TCLP: an online cancer cell line catalogue integrating HLA type, predicted neo-epitopes, virus and gene expression.

Loewer M., Sahin U., Castle J.C.

Genome Med. 7:118.1-118.7(2015).

Metabolite profiling stratifies pancreatic ductal adenocarcinomas into subtypes with distinct sensitivities to metabolic inhibitors.

Manning G., Settleman J., Hatzivassiliou G., Evangelista M.

Proc. Natl. Acad. Sci. U.S.A. 112:E4410-E4417(2015).

A resource for cell line authentication, annotation and quality control.

Neve R.M.

Nature 520:307-311(2015).

A comprehensive transcriptional portrait of human cancer cell lines.

Settleman J., Seshagiri S., Zhang Z.-M.

Nat. Biotechnol. 33:306-312(2015).

KRAS mutational subtype and copy number predict in vitro response of human pancreatic cancer cell lines to MEK inhibition.

Linnartz R., Zubel A., Slamon D.J., Finn R.S.

Br. J. Cancer 111:1788-1801(2014).

Breakpoint analysis of transcriptional and genomic profiles uncovers novel gene fusions spanning multiple human cancer types.

West R.B., Pollack J.R.

PLoS Genet. 9:E1003464-E1003464(2013).

Genetically defined subsets of human pancreatic cancer show unique in vitro chemosensitivity.

Iacobuzio-Donahue C.A., Eshleman J.R.

Clin. Cancer Res. 18:6519-6530(2012).

Essential gene profiles in breast, pancreatic, and ovarian cancer cells.

Rottapel R., Neel B.G., Moffat J.

Cancer Discov. 2:172-189(2012).

The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.

Morrissey M.P., Sellers W.R., Schlegel R., Garraway L.A.

Nature 483:603-607(2012).

A resource for analysis of microRNA expression and function in pancreatic ductal adenocarcinoma cells.

Mendell J.T.

Cancer Biol. Ther. 8:2013-2024(2009).

Molecular cytogenetic characterization of pancreas cancer cell lines reveals high complexity chromosomal alterations.

Ried T., Schrock E., Perlman E.J., Jaffee E.M.

Cytogenet. Genome Res. 118:148-156(2007).

Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.

Kern S.E.

Cancer Res. 66:7920-7928(2006).

Development and characterization of a cytokine-secreting pancreatic adenocarcinoma vaccine from primary tumors for use in clinical trials.

Thomas M., Greten T.F., Hruban R.H., Yeo C.J., Griffin C.A.

Cancer J. Sci. Am. 4:194-203(1998).