BICR 78Homo sapiens (Human)Cancer cell line

Also known as: Beatson Institute for Cancer Research 78, BICR78, BICR-78

🤖 AI SummaryBased on 8 publications

Quick Overview

Human squamous cell carcinoma cell line with p53 mutations and chromosomal abnormalities.

Detailed Summary

BICR 78 is a human squamous cell carcinoma cell line derived from head and neck tumors. It exhibits p53 mutations and chromosomal abnormalities, including loss of heterozygosity (LOH) at multiple loci. This cell line is used in research to study the genetic alterations associated with cancer progression and immortality. BICR 78 shows characteristics of immortalized cells, such as indefinite proliferation in vitro, and is part of a panel of cell lines used to investigate the molecular mechanisms of cancer development and therapeutic responses.

Research Applications

Study of genetic alterations in cancer progressionInvestigation of p53 mutations and their role in tumorigenesisAnalysis of chromosomal abnormalities and LOH in cancer cellsResearch on immortalization mechanisms in cancer cells

Key Characteristics

p53 mutationsChromosomal abnormalitiesLoss of heterozygosity at multiple lociImmortalized cell line with indefinite proliferation
Generated on 6/18/2025

Basic Information

Database IDCVCL_2315
SpeciesHomo sapiens (Human)
Tissue SourceOral cavity, alveolar ridge[UBERON:UBERON_0004103]

Donor Information

Age CategoryUnknown
SexMale

Disease Information

DiseaseSquamous cell carcinoma of the oral cavity
LineageHead and Neck
SubtypeOral Cavity Squamous Cell Carcinoma
OncoTree CodeOCSC

DepMap Information

Source TypeSigma-Aldrich
Source IDACH-001332_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Pro177Leu (c.530C>T)Unspecified-PubMed=8412323, PubMed=7727782
MutationSimpleTP53p.Cys176Phe (c.527G>T)Unspecified-PubMed=8221663
MutationSimpleTP53p.Gln38Ter (c.112C>T)Heterozygous-Unknown, Unknown
MutationUnexplicitPARD3Ex3-7delHomozygous-PubMed=20215515

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
12
D13S317
12
D16S539
11,12
D18S51
13,19
D21S11
33.2
D3S1358
18
D5S818
11
D7S820
10,11
D8S1179
14
FGA
19
Penta D
10
Penta E
11,13
TH01
6,9.3
TPOX
9,10
vWA
15,16
Gene Expression Profile
Gene expression levels and statistical distribution
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Full DepMap dataset with combined data across cell lines

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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).

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).

A landscape of pharmacogenomic interactions in cancer.";

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

Cell 166:740-754(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).

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).

A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers.

Haber D.A.

Cancer Res. 70:2158-2164(2010).

Increased dosage and amplification of the focal adhesion kinase gene in human cancer cells.

Keith W.N., Frame M.C.

Oncogene 18:5646-5653(1999).

Evidence for the inactivation of multiple replicative lifespan genes in immortal human squamous cell carcinoma keratinocytes.

Parkinson E.K.

Oncogene 14:1955-1964(1997).

Cellular immortality: a late event in the progression of human squamous cell carcinoma of the head and neck associated with p53 alteration and a high frequency of allele loss.

Edington K.G., Loughran O.P., Berry I.J., Parkinson E.K.

Mol. Carcinog. 13:254-265(1995).