HTC-C3Homo sapiens (Human)Cancer cell line

Also known as: HTCC3, HTC C3, HTC/C3

🤖 AI SummaryBased on 6 publications

Quick Overview

Human anaplastic thyroid cancer cell line for cancer research.

Detailed Summary

HTC-C3 is a human anaplastic thyroid cancer cell line derived from a patient with anaplastic thyroid carcinoma. It is widely used in research to study the molecular mechanisms of thyroid cancer progression and drug resistance. The cell line exhibits characteristics of aggressive tumor behavior, including rapid proliferation and resistance to various chemotherapeutic agents. Research on HTC-C3 has contributed to understanding the role of genetic alterations, such as DUSP26 amplification and TERT promoter mutations, in cancer development and therapeutic response. These findings are critical for developing targeted therapies and improving patient outcomes.

Research Applications

Molecular mechanisms of thyroid cancer progressionDrug resistance studiesGenetic alterations in cancer developmentTherapeutic response analysis

Key Characteristics

Rapid proliferationResistance to chemotherapeutic agentsDUSP26 amplificationTERT promoter mutations
Generated on 6/16/2025

Basic Information

Database IDCVCL_1295
SpeciesHomo sapiens (Human)
Tissue SourcePleural effusion[UBERON:UBERON_0000175]

Donor Information

Age44
Age CategoryAdult
SexFemale

Disease Information

DiseaseAnaplastic thyroid carcinoma
LineageThyroid
SubtypeAnaplastic Thyroid Cancer
OncoTree CodeTHAP

DepMap Information

Source TypeDSMZ
Source IDACH-001350_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleTP53p.Pro152Leu (c.455C>T)Unspecified-PubMed=21602893
MutationSimpleTERTc.1-124C>T (c.228C>T) (C228T)UnspecifiedIn promoterfrom parent cell line Hep-G2
MutationSimpleBRAFp.Val600Glu (c.1799T>A)Unspecified-PubMed=26214590

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
11,12
D13S317
10,12
D16S539
9,12
D18S51
14,17
D19S433
14
D21S11
29,30
D2S1338
17,23
D3S1358
16
D5S818
11,12
D7S820
11,12
D8S1179
12,14
FGA
21,22
Penta D
9
Penta E
11,16
TH01
6,7
TPOX
8,9
vWA
14,15
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).

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).

Comprehensive genetic characterization of human thyroid cancer cell lines: a validated panel for preclinical studies.

Fagin J.A., Schweppe R.E.

Clin. Cancer Res. 25:3141-3151(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).

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

Neve R.M.

Nature 520:307-311(2015).

Frequent somatic TERT promoter mutations in thyroid cancer: higher prevalence in advanced forms of the disease.

Ibrahimpasic T., Ghossein R.A., Fagin J.A.

J. Clin. Endocrinol. Metab. 98:E1562-E1566(2013).

Signatures of mutation and selection in the cancer genome.";

Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.

Nature 463:893-898(2010).

A novel amplification target, DUSP26, promotes anaplastic thyroid cancer cell growth by inhibiting p38 MAPK activity.

Yu W., Imoto I., Inoue J., Onda M., Emi M., Inazawa J.

Oncogene 26:1178-1187(2007).

Lack of a point mutation of human DNA topoisomerase II in multidrug-resistant anaplastic thyroid carcinoma cell lines.

Satake S., Sugawara I., Watanabe M., Takami H.

Cancer Lett. 116:33-39(1997).

Establishment of a human undifferentiated thyroid cancer cell line producing several growth factors and cytokines.

Kitamura N., Yamamoto I., Konishi J., Mori T., Imura H.

Cancer 65:1971-1979(1990).

Role of p53 mutations in endocrine tumorigenesis: mutation detection by polymerase chain reaction-single strand conformation polymorphism.

Yoshimoto K., Iwahana H., Fukuda A., Sano T., Saito S., Itakura M.

Cancer Res. 52:5061-5064(1992).