Acral Lentiginous Melanoma Cell Line - (HBL (MM001))
Product Code:
ABM-T8080
ABM-T8080
Host Type:
Human
Human
Regulatory Status:
RUO
RUO
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| ABM-T8080 | 1x10^6 cells / 1.0 ml | Enquire | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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This product comes from: Canada.
Typical lead time: 10-14 working days.
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Typical lead time: 10-14 working days.
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Further Information
Description:
This melanoma cell line panel is unique from all other available melanoma cell lines as these cells have been raised under conditions that prevent phenotype switching. MM001/HBL is sensitive to TKI (Dasatinib, Sunitinib); (MM001-R (HBL-R) line with acquired resistance to TKI). This cell line is applicable for high-throughput screening/Drug testing and 3D cell cultures. MM001/HBL is a Suitable transfection host and is tumorigenic: cells produce xenograft tumors when injected into immunocompromised mice. Note: This cell line should be cited in a scientific publication as: HBL (MM001). Additional cell lines from this panel:Cat. T8080 - Acral Lentiginous Melanoma Cell Line (HBL (MM001))Cat. T8081 - Acral Lentiginous Melanoma Cell Line (MM011/LND1)Cat. T8082 - Lymph Node Metastasis SS Melanoma Cell Line (MM029)Cat. T8083 - Bladder Metastasis Nodular Melanoma Cell Line (MM031)Cat. T8084 - Lymph Node Metastasis Melanoma Cell Line (MM034)Cat. T8085 - Superficial Spreading Melanoma Cell Line (MM052)Cat. T8086 - Lymph Node Metastasis Melanoma Cell Line (MM057)Cat. T8087 - Lymph Node Metastasis SS Melanoma Cell Line (MM074)Cat. T8088 - Lymph Node Metastasis SS Melanoma Cell Line (MM165)
Donor History:
Derived from a lymph node metastasis of a female with nodular melanoma
Growth Conditions:
PriCoat™ T25 Flasks (G299) or Applied Cell Extracellular Matrix (G422) are recommended for optimal cell culture. Ham's F10 Medium + 10% FBS + 2 mM L-Glutamine (G275) + 1% Penicillin/Streptomycin Solution (G255), 37.0°C, 5% CO2.
Growth Properties:
Adherent, proliferative melanocyte-like phenotype
Markers:
WT(BRAF, NRAS,PTEN,P53,MET), C-KIT(D820Y)
Population Doubling:
24-48
Split Ratio:
1:3 to 1:8
Tissue:
Lymph Node
References
Sabbah, M.; Krayem, M.; Najem, A.; Sales, F.; Miller, W.; Del Rincon, S.; Awada, A.; Ghanem, G.E.; Journe, F. Dasatinib Stimulates Its Own Mechanism of Resistance by Activating a CRTC3/MITF/Bcl-2 Pathway in Melanoma with Mutant or Amplified c-Kit. Mol Cancer Res 2021, 19, 1221?1233, doi:10.1158/1541-7786.MCR-20-1040 Krayem, M.; Journe, F.; Wiedig, M.; Morandini, R.; Sales, F.; Awada, A.; Ghanem, G. Prominent Role of Cyclic Adenosine Monophosphate Signalling Pathway in the Sensitivity of (WT)BRAF/(WT)NRAS Melanoma Cells to Vemurafenib. Eur. J. Cancer 2014, 50, 1310?1320, doi:10.1016/j.ejca.2014.01.021. Krayem, M.; Najem, A.; Journe, F.; Morandini, R.; Sales, F.; Awada, A.; Ghanem, G.E. Acquired Resistance to BRAFi Reverses Senescence-like Phenotype in Mutant BRAF Melanoma. Oncotarget 2018, 9, 31888?31903, doi:10.18632/oncotarget.25879. Soumoy, L.; Schepkens, C.; Krayem, M.; Najem, A.; Tagliatti, V.; Ghanem, G.E.; Saussez, S.; Colet, J.-M.; Journe, F. Metabolic Reprogramming in Metastatic Melanoma with Acquired Resistance to Targeted Therapies: Integrative Metabolomic and Proteomic Analysis. Cancers (Basel) 2020, 12, E1323, doi:10.3390/cancers12051323. Wouters, J.; Kalender-Atak, Z.; Minnoye, L.; Spanier, K.I.; De Waegeneer, M.; Bravo González-Blas, C.; Mauduit, D.; Davie, K.; Hulselmans, G.; Najem, A.; et al. Robust Gene Expression Programs Underlie Recurrent Cell States and Phenotype Switching in Melanoma. Nat Cell Biol 2020, 22, 986?998, doi:10.1038/s41556-020-0547-3. Verfaillie, A.; Imrichova, H.; Atak, Z.K.; Dewaele, M.; Rambow, F.; Hulselmans, G.; Christiaens, V.; Svetlichnyy, D.; Luciani, F.; Van den Mooter, L.; et al. Decoding the Regulatory Landscape of Melanoma Reveals TEADS as Regulators of the Invasive Cell State. Nature Communications 2015, 6, 6683, doi:10.1038/ncomms7683. Gembarska, A.; Luciani, F.; Fedele, C.; Russell, E.A.; Dewaele, M.; Villar, S.; Zwolinska, A.; Haupt, S.; de Lange, J.; Yip, D.; et al. MDM4 Is a Key Therapeutic Target in Cutaneous Melanoma. Nat Med 2012, 18, 10.1038/nm.2863, doi:10.1038/nm.2863. Aftimos, P.G.; Wiedig, M.; Langouo Fontsa, M.; Awada, A.; Ghanem, G.; Journe, F. Sequential Use of Protein Kinase Inhibitors Potentiates Their Toxicity to Melanoma Cells: A Rationale to Combine Targeted Drugs Based on Protein Expression Inhibition Profiles. Int. J. Oncol. 2013, 43, 919?926, doi:10.3892/ijo.2013.2008 Eves, P.; Haycock, J.; Layton, C.; Wagner, M.; Kemp, H.; Szabo, M.; Morandini, R.; Ghanem, G.; García-Borrón, J.C.; Jim?nez-Cervantes, C.; et al. Anti-Inflammatory and Anti-Invasive Effects of Alpha-Melanocyte-Stimulating Hormone in Human Melanoma Cells. Br J Cancer 2003, 89, 2004?2015, doi:10.1038/sj.bjc.6601349. Porcelli L., Guida G., Quatrale A.E., Cocco T., Sidella L., Maida I., Iacobazzi R.M., Ferretta A., Stolfa D.A., Strippoli S., Guida S., Tommasi S., Guida M., Azzariti A.Aurora kinase B inhibition reduces the proliferation of metastatic melanoma cells and enhances the response to chemotherapy. J. Transl. Med. 13:26.1-26.13(2015) doiI=10.1186/s12967-015-0385-4 Zanna P., Maida I., Grieco C., Guida S., Turpin Sevilla M.C., De Summa S., Tommasi S., Vena G.A., Filotico R., Guida G. Three novel human sporadic melanoma cell lines: signaling pathways controlled by MC1R, BRAF and beta-catenins. J. Biol. Regul. Homeost. Agents 27:131-14 PubMed=23489693 Mauduit, D.; Taskiran, I.I.; Minnoye, L.; Waegeneer, M. de; Christiaens, V.; Hulselmans, G.; Demeulemeester, J.; Wouters, J.; Aerts, S. Analysis of Long and Short Enhancers in Melanoma Cell States. eLife 2021, 10, doi:10.7554/eLife.71735. Huang, F.; Gon?alves, C.; Bartish, M.; R?my-Sarrazin, J.; Issa, M.E.; Cordeiro, B.; Guo, Q.; Emond, A.; Attias, M.; Yang, W.; et al. Inhibiting the MNK1/2-EIF4E Axis Impairs Melanoma Phenotype Switching and Potentiates Antitumor Immune Responses. J Clin Invest 2021, 131, doi:10.1172/JCI140752.
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| PriGrow X Series Medium for T8080 | ABM-TM8080 | Applied Biological Materials (abm) | Summary Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||

