MOLM-13Homo sapiens (Human)Cancer cell line
Also known as: Molm 13, Molm13, MOLM13
Quick Overview
MOLM-13 is a human acute myeloid leukemia cell line derived from MDS with FLT3-ITD mutation, used in cancer research.
Detailed Summary
Research Applications
Key Characteristics
Basic Information
Database ID | CVCL_2119 |
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Species | Homo sapiens (Human) |
Tissue Source | Peripheral blood[UBERON:UBERON_0000178] |
Donor Information
Age | 20 |
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Age Category | Adult |
Sex | Male |
Disease Information
Disease | Acute myeloid leukemia |
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Lineage | Myeloid |
Subtype | Acute Myeloid Leukemia |
OncoTree Code | AML |
DepMap Information
Source Type | DSMZ |
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Source ID | ACH-000362_source |
Known Sequence Variations
Type | Gene/Protein | Description | Zygosity | Note | Source |
---|---|---|---|---|---|
MutationUnexplicit | FLT3 | Internal tandem duplication (FLT3-ITD) | Unspecified | - | PubMed=12529668 |
Gene fusion | KMT2A | KMT2A-MLLT3, MLL-MLLT3, MLL-AF9 | - | - | PubMed=31701557 |
Haplotype Information (STR Profile)
Short Tandem Repeat (STR) profile for cell line authentication.
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).
Changes in apoptotic pathways in MOLM-13 cell lines after induction of resistance to hypomethylating agents.
Sulova Z., Breier A.
Int. J. Mol. Sci. 22:2076.1-2076.24(2021).
Quantitative proteomics of the Cancer Cell Line Encyclopedia.";
Sellers W.R., Gygi S.P.
Cell 180:387-402.e16(2020).
The LL-100 panel: 100 cell lines for blood cancer studies.";
MacLeod R.A.F., Nagel S., Steube K.G., Uphoff C.C., Drexler H.G.
Sci. Rep. 9:8218-8218(2019).
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).
Screening human cell lines for viral infections applying RNA-Seq data analysis.
Uphoff C.C., Pommerenke C., Denkmann S.A., Drexler H.G.
PLoS ONE 14:E0210404-E0210404(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).
The novel BET bromodomain inhibitor BI 894999 represses super-enhancer-associated transcription and synergizes with CDK9 inhibition in AML.
Gerstberger T., Zuber J., Savarese F., Kraut N.
Oncogene 37:2687-2701(2018).
Characterization of human cancer cell lines by reverse-phase protein arrays.
Liang H.
Cancer Cell 31:225-239(2017).
Hh/Gli antagonist in acute myeloid leukemia with CBFA2T3-GLIS2 fusion gene.
Pigazzi M., Martelli A.M., Basso G., Locatelli F., Pession A.
J. Hematol. Oncol. 10:26.1-26.5(2017).
Establishment and characterization of hypomethylating agent-resistant cell lines, MOLM/AZA-1 and MOLM/DEC-5.
Chung Y.-J., Lee J.-H.
Oncotarget 8:11748-11762(2017).
Immunophenotypic, cytogenetic, and mutational characterization of cell lines derived from myelodysplastic syndrome patients after progression to acute myeloid leukemia.
Campos D., Granada I., Junca J., Drexler H.G., Sole F., Buschbeck M.
Genes Chromosomes Cancer 56:243-252(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).
Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies.
Golub T.R., Root D.E., Hahn W.C.
Sci. Data 1:140035-140035(2014).
A resource for cell line authentication, annotation and quality control.
Neve R.M.
Nature 520:307-311(2015).
Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms.
Haferlach T., Shirahige K., Miyano S., Ogawa S.
Nat. Genet. 45:1232-1237(2013).
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).
Selective FLT3 inhibition of FLT3-ITD+ acute myeloid leukaemia resulting in secondary D835Y mutation: a model for emerging clinical resistance patterns.
Raynaud F.I., Eccles S.A., Linardopoulos S.
Leukemia 26:1462-1470(2012).
JAK2 V617F tyrosine kinase mutation in cell lines derived from myeloproliferative disorders.
Quentmeier H., MacLeod R.A.F., Zaborski M., Drexler H.G.
Leukemia 20:471-476(2006).
Identification of two MLL-MLLT3 (alias MLL-AF9) chimeric transcripts in the MOLM-13 cell line.
Pession A.
Cancer Genet. Cytogenet. 154:96-97(2004).
Malignant hematopoietic cell lines: in vitro models for the study of MLL gene alterations.
Drexler H.G., Quentmeier H., MacLeod R.A.F.
Leukemia 18:227-232(2004).
FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidy.
Tsuchida M., Sugita K., Ida K., Hayashi Y.
Blood 103:1085-1088(2004).
FLT3 mutations in acute myeloid leukemia cell lines.";
Quentmeier H., Reinhardt J., Zaborski M., Drexler H.G.
Leukemia 17:120-124(2003).
Corrigendum to: Frequent microsatellite instability and BAX mutations in T cell acute lymphoblastic leukemia cell lines Leukemia Research 24 (2000), 255-262.
Inoue K., Kohno T., Takakura S., Hayashi Y., Mizoguchi H., Yokota J.
Leuk. Res. 25:275-278(2001).
Frequent microsatellite instability and BAX mutations in T cell acute lymphoblastic leukemia cell lines.
Inoue K., Kohno T., Takakura S., Hayashi Y., Mizoguchi H., Yokota J.
Leuk. Res. 24:255-262(2000).
p53 alterations in human leukemia-lymphoma cell lines: in vitro artifact or prerequisite for cell immortalization?
Uphoff C.C.
Leukemia 14:198-206(2000).
Tandem duplication of the FLT3 gene is found in acute lymphoblastic leukaemia as well as acute myeloid leukaemia but not in myelodysplastic syndrome or juvenile chronic myelogenous leukaemia in children.
Kobayashi M., Bessho F., Yanagisawa M., Hayashi Y.
Br. J. Haematol. 105:155-162(1999).
Two acute monocytic leukemia (AML-M5a) cell lines (MOLM-13 and MOLM-14) with interclonal phenotypic heterogeneity showing MLL-AF9 fusion resulting from an occult chromosome insertion, ins(11;9)(q23;p22p23).
Katayama Y., Kimura G., Fujii N., Omoto E., Harada M., Orita K.
Leukemia 11:1469-1477(1997).
The leukemia-lymphoma cell line factsbook.";
Drexler H.G.
(In book) ISBN 9780122219702; pp.1-733; Academic Press; London; United Kingdom (2001).