KHM-1BHomo sapiens (Human)Cancer cell line

Also known as: KHM1B

🤖 AI SummaryBased on 8 publications

Quick Overview

Human B-cell line for cancer research

Detailed Summary

KHM-1B is a human B-cell line derived from multiple myeloma. It is used in research to study the molecular mechanisms of cancer, particularly in the context of myeloma and plasma cell leukemia. The cell line is characterized by its ability to grow in culture and is utilized for drug sensitivity testing and genetic studies. It is part of a larger collection of cell lines that are essential for understanding the heterogeneity of cancer and developing targeted therapies.

Research Applications

Cancer researchDrug sensitivity testingGenetic studies

Key Characteristics

Human B-cell lineUsed in multiple myeloma studiesGrows in culture
Generated on 6/19/2025

Basic Information

Database IDCVCL_2972
SpeciesHomo sapiens (Human)
Tissue SourcePleural effusion[UBERON:UBERON_0000175]

Donor Information

Age53
Age CategoryAdult
SexMale

Disease Information

DiseaseMultiple myeloma
LineageLymphoid
SubtypePlasma Cell Myeloma
OncoTree CodePCM

DepMap Information

Source TypeHSRRB
Source IDACH-000564_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleNRASp.Gly12Cys (c.34G>T)HeterozygousIn 3% of the readsPubMed=34940123
MutationSimpleKRASp.Gly12Cys (c.34G>T)Unspecified-PubMed=21173094

Haplotype Information (STR Profile)

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

Amelogenin
X
CSF1PO
10
D13S317
11
D16S539
9
D18S51
16,18
D21S11
30,31
D3S1358
15
D5S818
11
D7S820
10
D8S1179
11,12
FGA
24
Penta D
9,12
Penta E
8,16
TH01
6
TPOX
11
vWA
14,17
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

Evaluating the efficacy of multiple myeloma cell lines as models for patient tumors via transcriptomic correlation analysis.

Sirota M., Wiita A.P.

Leukemia 34:2754-2765(2020).

Next-generation characterization of the Cancer Cell Line Encyclopedia.

Sellers W.R.

Nature 569:503-508(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).

Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines.

Yang H.H., Koeffler H.P.

BMC Cancer 18:940.1-940.13(2018).

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).

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).

Characterization of MYC translocations in multiple myeloma cell lines.

Dib A., Gabrea A., Glebov O.K., Bergsagel P.L., Kuehl W.M.

J. Natl. Cancer Inst. Monogr. 39:25-31(2008).

Promiscuous mutations activate the noncanonical NF-kappaB pathway in multiple myeloma.

Stewart A.K., Carpten J.D., Bergsagel P.L.

Cancer Cell 12:131-144(2007).

Malignant hematopoietic cell lines: in vitro models for the study of multiple myeloma and plasma cell leukemia.

Drexler H.G., Matsuo Y.

Leuk. Res. 24:681-703(2000).

Establishment and characterization of an amylase-producing human myeloma cell line.

Matsuzaki H., Hata H., Takeya M., Takatsuki K.

Blood 72:978-982(1988).

Genetic analysis of amylase-producing cell lines: ectopic activation of the amylase gene by translocation.

Hata H., Matsuzaki H., Sanada I., Takatsuki K.

Jpn. J. Clin. Oncol. 20:246-251(1990).

Multiple myeloma cell lines.";

Jernberg-Wiklund H., Nilsson K.

(In book chapter) Human cell culture. Vol. 3. Cancer cell lines part 3; Masters J.R.W., Palsson B.O. (eds.); pp.81-155; Kluwer Academic Publishers; New York; USA (2000).

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