Origin of the U87MG glioma cell line: Good news and bad news

The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity

Barretina, J., Caponigro, G., Stransky, N., Venkatesan, K., Margolin, A. A., Kim, S., Wilson, C. J., Lehár, J., Kryukov, G. V., Sonkin, D., et al. (2012) · Nature · doi:10.1038/nature11003 · Cited by 7,950

Tumor stem cells derived from glioblastomas cultured in bFGF and EGF more closely mirror the phenotype and genotype of primary tumors than do serum-cultured cell lines

Lee, J., Kotliarova, S. E., Kotliarov, Y., Li, A., Su, Q., Donin, N. M., Pastorino, S., Purow, B. W., Christopher, N., Zhang, W., et al. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.03.030 · Cited by 2,345

Glioma Stem Cell Lines Expanded in Adherent Culture Have Tumor-Specific Phenotypes and Are Suitable for Chemical and Genetic Screens

Pollard, S. M., Yoshikawa, K., Clarke, I. D., Danovi, D., Stricker, S., Russell, R., Bayani, J., Head, R., Lee, M., Bernstein, M., et al. (2009) · Cell Stem Cell · doi:10.1016/j.stem.2009.03.014 · Cited by 1,025

LONG TERM CULTURE OF NORMAL AND NEOPLASTIC HUMAN GLIA

Pontén, J., & Macintyre, E. H. (1968) · Acta Pathologica Microbiologica Scandinavica · doi:10.1111/j.1699-0463.1968.tb03502.x · Cited by 721

Absence of HeLa Cell Contamination in 169 Cell Lines Derived From Human Tumors2

Fogh, J., Wright, W. C., & Loveless, J. D. (1977) · JNCI: Journal of the National Cancer Institute · doi:10.1093/jnci/58.2.209 · Cited by 663

Check your cultures! A list of cross‐contaminated or misidentified cell lines

Capes‐Davis, A., Theodosopoulos, G., Atkin, I., Drexler, H. G., Kohara, A., MacLeod, R. A. F., Masters, J. R., Nakamura, Y., Reid, Y. A., Reddel, R. R., et al. (2010) · International Journal of Cancer · doi:10.1002/ijc.25242 · Cited by 520 · cited 1×

The Human Glioblastoma Cell Culture Resource: Validated Cell Models Representing All Molecular Subtypes

Xie, Y., Bergström, T., Jiang, Y., Johansson, P., Marinescu, V. D., Lindberg, N., Segerman, A., Wicher, G., Niklasson, M., Baskaran, S., et al. (2015) · EBioMedicine · doi:10.1016/j.ebiom.2015.08.026 · Cited by 329

Cell line misidentification: the beginning of the end

American Type Culture Collection Standards Development Organization Workgroup ASN-0002 (2010) · Nature Reviews Cancer · doi:10.1038/nrc2852 · Cited by 266

DNA fingerprinting in forensics: past, present, future

Roewer, L. (2013) · Investigative Genetics · doi:10.1186/2041-2223-4-22 · Cited by 182

The Beginning of the End

Schraer, L., Borum, I., & Sathyan, T. G. (1995) · Cited by 113

The noncoding RNA LINC00152 conveys contradicting effects in different glioblastoma cells

Binder, S., Zipfel, I., Müller, C., Wiedemann, K., Schimmelpfennig, C., Pfeifer, G., Reiche, K., Hauschildt, S., Lehmann, J., Koehl, U., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-97533-8 · Cited by 6

Tumorigenicity Assessment of Human Cancer Cell Lines Xenografted on Immunodeficient Mice as Positive Controls of Tumorigenicity Testing

Oh, S., Gu, E.-Y., Han, J., Lee, B., Moon, K., Kim, Y., & Han, K.-H. (2022) · International Journal of Toxicology · doi:10.1177/10915818221124573 · Cited by 8

Emerging Pathogenic and Prognostic Significance of Paired Box 3 (PAX3) Protein in Adult Gliomas

Angelopoulou, E., Paudel, Y. N., & Piperi, C. (2019) · Translational Oncology · doi:10.1016/j.tranon.2019.07.001 · Cited by 6

Molecular determinants of interaction between glioblastoma CD133+ cancer stem cells and extracellular matrix

Bryukhovetskiy, I., Khotimchenko, Y. S., & Шевченко, В. Е. (2019) · Annals of Oncology · doi:10.1093/annonc/mdz413.016 · Cited by 6

Development of a highly optimized procedure for the discovery of RNA G-quadruplexes by combining several strategies

Turcotte, M.-A., Bolduc, F., Vannutelli, A., Mitteaux, J., Monchaud, D., & Perreault, J. (2023) · Biochimie · doi:10.1016/j.biochi.2023.07.014 · Cited by 6

Incorporating Targeted Therapy Into Neuro-Oncology Practice

Geurts, M., Blaquier, J. B., Wijnenga, M. M. J., Kamson, D. O., & de la Fuente, M. I. (2025) · American Society of Clinical Oncology Educational Book · doi:10.1200/edbk-25-473324 · Cited by 5

Molecular characteristics of single patient-derived glioma stem-like cells from primary and recurrent glioblastoma

Shi, J., Dong, X., Han, W., Zhou, P., Liu, L., Wang, H., Jiang, Q., Li, H., Cheng, S., Li, S., et al. (2021) · Anti-Cancer Drugs · doi:10.1097/cad.0000000000001217 · Cited by 5

Using short tandem repeat profiling to validate cell lines in biobanks

Kosobokova, E. N., Malchenkova, A. A., Kalinina, N. A., & Kosorukov, V. S. (2022) · CARDIOVASCULAR THERAPY AND PREVENTION · doi:10.15829/1728-8800-2022-3386 · Cited by 5

Bioactive Compounds, Antioxidant Activity, and Antiproliferative Potential on Glioblastoma Cells of Selected Stone Fruit Juices

Raucher, D., Rowsey, M. E., Hinson, J., Ćorković, I., Lila, M. A., Šimunović, J., & Kopjar, M. (2024) · Processes · doi:10.3390/pr12071310 · Cited by 5

Valproic Acid and Celecoxib Enhance the Effect of Temozolomide on Glioblastoma Cells

Pak, O., Kosianova, A. A., Zaitsev, S., Sharma, A., Sharma, H. O., & Bryukhovetskiy, I. (2024) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/0118715273330268241008220702 · Cited by 5

Generation of patient-derived glioblastoma organoids: a comparative study of enzymatic digestion and mechanical fragmentation methods

Zhang, J., Liu, J., Shi, Y., Li, L., Wang, C., Rong, M., Tao, B., Tan, H., Deng, W., Cai, C., et al. (2024) · Cell organoid (Print) · doi:10.26599/co.2024.9410004 · Cited by 5

Targeting VPAC1 Receptors for Imaging Glioblastoma

Tripathi, S., Kean, R. B., Bongiorno, E. K., Hooper, D. C., Jin, Y., Wickstrom, E., McCue, P. A., & Thakur, M. L. (2019) · Molecular Imaging and Biology · doi:10.1007/s11307-019-01388-5 · Cited by 5

Tumor Specific Peptides Selected for Targeted Delivery of Therapeutic Agents to Glioma Human Cells

Voitova, A. A., Dmitrieva, M., Dymova, M. A., Vasileva, N. S., Nushtaeva, A. A., Richter, V. A., & Kuligina, E. V. (2019) · Russian Journal of Bioorganic Chemistry · doi:10.1134/s1068162019060384 · Cited by 5

Transforming growth factor-β mimics the key proteome properties of CD133− differentiated and CD133+ cancer stem cells in glioblastoma

Bryukhovetskiy, I., Шевченко, В. Е., Arnotskaya, N. E., Kushnir, T., Pak, O., Victor, Z., Zaitsev, S., Khotimchenko, Y. S., Bryukhovetskiy, A. S., Sharma, A., et al. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2020.03.007 · Cited by 5

Patient-Derived Xenotransplant of CNS Neoplasms in Zebrafish: A Systematic Review

Sarmiento, B. E., Callegari, S., Ghotme, K. A., & Akle, V. (2022) · Cells · doi:10.3390/cells11071204 · Cited by 5

From neural stem cells to glioblastoma: A natural history of GBM recapitulated in vitro

Almengló, C., Caamaño, P., Fraga, M., Devesa, J., Costoya, J. A., & Arce, V. M. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30409 · Cited by 5

Differential mitochondrial protein interaction profile between human translocator protein and its A147T polymorphism variant

Asih, P. R., Poljak, A., Kassiou, M., Ke, Y. D., & Ittner, L. M. (2022) · PLoS ONE · doi:10.1371/journal.pone.0254296 · Cited by 6

Glioblastoma utilizes fatty acids and ketone bodies for growth allowing progression during ketogenic diet therapyPreprint

Sperry, J., Condro, M. C., Guo, L., Braas, D., Vanderveer-Harris, N., Kim, K. K. O., Pope, W. B., Divakaruni, A. S., Lai, A., Christofk, H., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/659474 · Cited by 5

Hyaluronic Acid Influences Amino Acid Metabolism via Differential L‐Type Amino Acid Transporter 1 Expression in the U87‐Malignant Glioma Cell Line

Bale, A. A., Thammineni, S., Bhargava, R., & Harley, B. A. C. (2024) · Advanced NanoBiomed Research · doi:10.1002/anbr.202400107 · Cited by 4

Spatiotemporal Imaging of Catechol Aldehydes in Neural Tissue

Talbott, J. M., Wills, R. D., Shirke, R. P., Hassanein, L., Weinshenker, D., & Raj, M. (2025) · JACS Au · doi:10.1021/jacsau.4c01249 · Cited by 4

Hijacking migration: CXCL12-functionalized hydrogels as a new frontier in glioblastoma therapy

Khorramdelazad, H., Pourtorabi, S. M., Ghaffarinasab, M., & Sedghi, Z. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118921 · Cited by 4

Localized glioblastoma therapy using a tenascin-C inhibitor peptide-modified hyaluronic acid hydrogel

Loureiro, B., Gimondi, S., Guimarães, C. F., Correia, B. F. C., Castro, V. I. B., Pires, R. A., Reis, R., Ferreira, H., & Neves, N. M. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2026.150089 · Cited by 4

Promoting the nuclear retention of HMGB1 attenuates astrocyte senescence

Zhang, N., Yang, F., Shi, J., Tang, X., Fan, A., Li, W., Zhang, F., Chai, S., Chen, Q., Wang, C., et al. (2026) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03684-0 · Cited by 4

Modeling gliomas with organoids: Classification, fidelity, and guidelines for translational neuro-oncology

Hubert, C. G., Read, R. D., Miller, T. E., Kim, U., Wang, X., Ishan, M., Wang, Z., Miller, E., Sun, Y. Y., Lai, A., et al. (2026) · Neuro-Oncology · doi:10.1093/neuonc/noag085 · Cited by 4

Preclinical glioma models in neuro-oncology: enhancing translational research

Barachini, S., Morelli, M., Santonocito, O. S., & Mazzanti, C. M. (2023) · Current Opinion in Oncology · doi:10.1097/cco.0000000000000997 · Cited by 5

UBDP1 pseudogene and UBD network competitively bind miR‑6072 to promote glioma progression

Hong, F., Gong, Z., Chen, C., Hua, T., Huang, Q., Liu, Y., Ma, P., Zhang, X., Wang, H., & Chen, J. (2024) · International Journal of Oncology · doi:10.3892/ijo.2024.5617 · Cited by 4

Expression of STAT3 and hypoxia markers in long-term surviving malignant glioma patients

Dvořáková, K., Skarková, V., Vítovcová, B., Soukup, J., Vošmiková, H., Pleskacova, Z., Skarka, A., Bartos, M. C., Krůpa, P., Kašparová, P., et al. (2024) · BMC Cancer · doi:10.1186/s12885-024-12221-w · Cited by 4

Unite and Conquer: Association of Two G-Quadruplex Aptamers Provides Antiproliferative and Antimigration Activity for Cells from High-Grade Glioma Patients

Pavlova, S., Fab, L. V., Dzarieva, F., Ryabova, A. V., Revishchin, A. V., Panteleev, D., Antipova, O. M., Usachev, D. Y., Kopylov, A. M., & Pavlova, G. V. (2024) · Pharmaceuticals · doi:10.3390/ph17111435 · Cited by 4

Dissection of Neurochemical Pathways Across Complexity and Scale

Abbondanza, A., Kim, N., Lima‐Filho, R. A. S., Amin, A., Anversa, R. G., Almeida, F. B., Cardozo, P. L., Carello‐Collar, G., Carsana, E. V., Folarin, R. O., et al. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70160 · Cited by 4

Guide for Selection of Relevant Cell Lines During the Evaluation of new Anti-Cancer Compounds

Ruiz-Moreno, A. J., Torres-Barrera, P., Velázquez-Paniagua, M., Dömling, A. S. S., & Velasco-Velázquez, M. A. (2018) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520618666180220120544 · Cited by 5

Creation and Development of Patient-Derived Organoids for Therapeutic Screening in Solid Cancer

Hicks, W. H., Bird, C. E., Gattie, L. C., Shami, M. E., Traylor, J. I., Shi, D. D., McBrayer, S. K., & Abdullah, K. G. (2022) · Current Stem Cell Reports · doi:10.1007/s40778-022-00211-2 · Cited by 4

Cell Line Detective Work

Capes‐Davis, A. (2018) · Advances in Molecular Pathology · doi:10.1016/j.yamp.2018.06.011 · Cited by 4

Gadofosveset‑enhanced MRI as simple surrogate parameter for real‑time evaluation of the initial tumour vessel infarction by retargeted tissue factor tTF‑NGR

H�ink, A., ten Persigehl, T., Kwiecien, R., Balthasar, M., Mesters, R. M., Berdel, W. E., Heindel, W. L., Bremer, C., & Schw�ppe, C. (2018) · Oncology Letters · doi:10.3892/ol.2018.9638 · Cited by 4

APOL4-mediated intracellular cholesterol trafficking is essential for glioblastoma cell growth

Zhang, M., Yang, T., & Qian, Y. (2025) · BMC Cancer · doi:10.1186/s12885-025-14316-4 · Cited by 3

Morphofunctional Heterogeneity and Plasticity of Glioblastoma Cells Induced to Senescence by Temozolomide

da Rosa, S. A., Oliveira, H. M., de Mendonça, L. B., de Oliveira, N. B., Jaeger, M. D. C., Pereira, L. C., Oliveira, F. D., Santos‐Sousa, D., Saez‐Calazans, F., Lenz, L. S., et al. (2026) · Aging Cell · doi:10.1111/acel.70477 · Cited by 3

Establishment of a novel benign meningioma cell line spontaneously immortalized under hypoxic conditions

Ishikawa, T., Matsuda, M., Ishikawa, H., Toyomura, J., Ohyama, A., Sakamoto, N., Zaboronok, A., & Ishikawa, E. (2024) · Human Cell · doi:10.1007/s13577-024-01151-1 · Cited by 3

Enhancing glioblastoma therapy: unveiling synergistic anticancer effects of Onalespib - radiotherapy combination therapy

Uffenorde, J., Hariri, M., Papalanis, E., Staffas, A., Berg, J., Stenerlöw, B., Berglund, H., Malmberg, C., & Spiegelberg, D. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1451156 · Cited by 3

Recent advances in 3D printing applications for CNS tumours

Awuah, W. A., Karkhanis, S., Ben-Jaafar, A., Kong, J. S. H., Mannan, K. M., Nkrumah-Boateng, P. A., Tan, J. K., Adeleke, O. A., Shet, V., Shah, M. H., et al. (2025) · European journal of medical research · doi:10.1186/s40001-025-02483-w · Cited by 3

Cell Behavior and Complex Mechanical Properties of 3D Printed Cell‐Laden Alginate‐Gelatin Macroporous Mesostructures

Murenu, N., Faber, J., Soufivand, A. A., Buss, M., Schaefer, N., & Budday, S. (2025) · Macromolecular Bioscience · doi:10.1002/mabi.202500204 · Cited by 3

Anti-cancer effect of Cissus quadrangularis on human glioblastoma cells

Cheng, B., Wei, Y., Guerra, L., Shirvani-Arani, R., Balderas, S., Valdez, L., Tsin, A. T. C., & Fang, X. (2023) · RPS Pharmacy and Pharmacology Reports · doi:10.1093/rpsppr/rqad014 · Cited by 3

Biophysical insights into OR2T7: Investigation of a potential prognostic marker for glioblastoma

Sharp, A. K., Newman, D. M., LIBONATE, G. P., Borns-Stern, M., Bevan, D. R., Brown, A. M., & Anandakrishnan, R. (2022) · Biophysical Journal · doi:10.1016/j.bpj.2022.05.009 · Cited by 3

Lactate does not replace glucose for maintaining the viability of mouse and human glioma cells

Miller, E. E., Duraj, T., Ta, N. L., Lee, D. C., Mukherjee, P., Shaver, O., & Seyfried, T. N. (2025) · ONCOLOGIE · doi:10.1515/oncologie-2025-0306 · Cited by 2

Primary glioma cell culture: from monolayer to organoids

Pristyazhnyuk, I. E., Stupak, E. V., Stupak, V. V., & Menzorov, A. G. (2025) · PROTOPLASMA · doi:10.1007/s00709-025-02137-y · Cited by 2

Potential therapeutic targeting of BK Ca channels in glioblastoma treatment

Maliszewska‐Olejniczak, K., Pytlak, K., Jaworowska, S., Kulawiak, B., & Bednarczyk, P. (2025) · Molecular Oncology · doi:10.1002/1878-0261.70167 · Cited by 2

Aggressive Glioblastoma Cells Enhance the Migratory Persistence and Velocity of Less Aggressive Cells to Promote Tumor Dissemination

Mohand, F.-E. A., Yemini, S., Cojocari, I., Rubinstein, A., Zemel, A., & Kravchenko‐Balasha, N. (2026) · Small · doi:10.1002/smll.202508142 · Cited by 2

DIVERSet JAG Compounds Inhibit Topoisomerase II and Are Effective Against Adult and Pediatric High-Grade Gliomas

Howarth, A., Simms, C., Kerai, N., Allen, O., Mihajluk, K., Madureira, P. A., Sokratous, G., Cragg, S. M., Lee, S. Y., Morley, A. D., et al. (2019) · Translational Oncology · doi:10.1016/j.tranon.2019.07.007 · Cited by 2

Expression of Concern on “Pseudolaric Acid B Induces Caspase-Dependent and Caspase-Independent Apoptosis in U87 Glioblastoma Cells”

Medicine, E.-B. C. A. A. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/4959838 · Cited by 2

Establishment and Comprehensive Molecular Characterization of an Immortalized Glioblastoma Cell Line from a Brazilian Patient

da Silva, F. F., Lupinacci, F. C. S., Elias, B. D. D. S., Beserra, A. D. O., Sanematsu, P., Roffé, M., Kulikowski, L. D., Costa, F. D., Santos, T. G., & Hajj, G. N. M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242115861 · Cited by 2

A machine learning–assisted systematic review of preclinical glioma modeling: Is practice changing with the times?

Hirst, T. C., Wilson, E., Browne, D., & Sena, E. S. (2024) · Neuro-Oncology Advances · doi:10.1093/noajnl/vdae193 · Cited by 2

ATP1A3 Acts as a Potential Anti-oncogene in Glioblastoma via the Antagonizing Interaction with Small Nuclear Ribonucleoprotein Polypeptide G

Zou, S., Qin, B., Chen, Q., Shen, Z., Liu, Q., Zhu, X., & Lan, Y. (2025) · Current Neuropharmacology · doi:10.2174/011570159x361656250128073206 · Cited by 2

Good Cell Culture Practice (GCCP)

OECD (2018) · OECD series on testing and assessment · doi:10.1787/9789264304796-16-en · Cited by 2

Applications of noncoding RNAs in brain cancer patients

Grabowska, M., Misiorek, J. O., Zarębska, Ż., & Rolle, K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-824550-7.00006-0 · Cited by 2

Test and reference/control items

OECD (2018) · OECD series on testing and assessment · doi:10.1787/9789264304796-11-en · Cited by 2

MiR-218 Targeted Regulation of Robol Expression Regulates Proliferation, Invasion and Migration of Glioma Cells

Zhang, R., Jiang, W., Liu, Z., Hou, P., & Zhang, S. (2022) · Cellular and Molecular Biology · doi:10.14715/cmb/2022.68.5.27 · Cited by 2

Tumoricidal, Temozolomide- and Radiation-Sensitizing Effects of KCa3.1 K+ Channel Targeting In Vitro Are Dependent on Glioma Cell Line and Stem Cell Fraction

Stransky, N., Ganser, K., Naumann, U., Huber, S. M., & Ruth, P. (2022) · Cancers · doi:10.3390/cancers14246199 · Cited by 2

1‐Naphthaleneacetic Acid Improved the In Vitro Cell Culturing by Inhibiting Apoptosis

Wang, Z., Li, F., Feng, C., Zheng, D., Pang, Z., Ma, Y., Xu, Y., Yang, C., Li, X., Peng, S., et al. (2024) · Advanced Biology · doi:10.1002/adbi.202300593 · Cited by 1

Serum Shock Enhances Endogenous Melatonin Production and Mitochondrial Gene Regulation in U87-MG Glioblastoma Cells

Balkhi, S., Jazi, M. S., Samaei, N. M., Rezaie, N., & Farahmandrad, M. (2025) · OBM Genetics · doi:10.21926/obm.genet.2503301 · Cited by 1

BLVRA promotes glioblastoma progression by regulating fatty acid metabolism

Li, L., Yao, J.-H., Feng, J. H., Qi, Z., Zhan, M.-S., San, H.-B., & Wang, X. (2025) · Scientific Reports · doi:10.1038/s41598-025-19026-2 · Cited by 1

Invasive properties of patient-derived glioblastoma cells after reversible electroporation in vitro

Blažič, A., Majc, B., Novak, M., Breznik, B., & Rems, L. (2025) · Radiology and Oncology · doi:10.2478/raon-2025-0058 · Cited by 1

Targeting leucine-rich repeat kinase 2 overcomes resistance to oncolytic herpes simplex virus-based therapies in glioblastoma

Qin, Y., Liang, Z., Yu, M., Lin, N., Wang, N., Huang, X., Chen, S., Peng, Q., Lin, Y., Wang, H., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-70132-9 · Cited by 1

Platelet-derived thromboxane A2 induces cyclooxygenase-2 and epithelial-mesenchymal transition marker genes in U-87MG human glioblastoma cells

Berardino, S. D., Contursi, A., Tacconelli, S., Ahfaz, H. A., & Patrignani, P. (2026) · Bleeding Thrombosis and Vascular Biology · doi:10.4081/btvb.2026.443 · Cited by 1

Neuropilin-1-Targeted Cell-Penetrating Tandem Peptide–Drug Conjugate Exhibits Potent In Vivo Antiglioma and Antiangiogenic Activity

Ranđelović, I., Baranyai, Z., Stipsicz, B., Surguta, S. E., Méhes, E., Jezsó, B., Biri‐Kovács, B., Horváth, L. B., Lakatos, L., Bősze, S. E., et al. (2026) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5c03835 · Cited by 1

Decellularized In Vitro Capillaries for Studies of Metastatic Tendency and Selection of Treatment

Huttala, O., Loreth, D., Staff, S. M., Tanner, M., Wikman, H., & Ylikomi, T. J. (2022) · Biomedicines · doi:10.3390/biomedicines10020271 · Cited by 1

Expression of Concern: ZEB2 Mediates Multiple Pathways Regulating Cell Proliferation, Migration, Invasion, and Apoptosis in Glioma

ONE, P. (2020) · PLoS ONE · doi:10.1371/journal.pone.0231386 · Cited by 1

Combining a noble gas with radiotherapy: glutamate receptor antagonist xenon may act as a radiosensitizer in glioblastoma

Büttner, T., Maerevoet, M. K. E., Giordano, F. A., Veldwijk, M. R., Herskind, C., & Ruder, A. M. (2024) · Radiation Oncology · doi:10.1186/s13014-023-02395-1 · Cited by 1

Standardisation and accreditation bodies

OECD (2018) · OECD series on testing and assessment · doi:10.1787/9789264304796-20-en · Cited by 1

Storage and retention of records and materials

OECD (2018) · OECD series on testing and assessment · doi:10.1787/9789264304796-15-en · Cited by 1

Roles and responsibilities

OECD (2018) · OECD series on testing and assessment · doi:10.1787/9789264304796-6-en · Cited by 1

Glioblastoma organoid technology: an emerging preclinical models for drug discovery

Batara, D. C., Zhou, S., Choi, M., & Kim, S.-H. (2022) · Organoid · doi:10.51335/organoid.2022.2.e7 · Cited by 1

Distinguishing between Normal and Cancer Cells Using Autoencoder Node SaliencyPreprint

Fan, Y. J., Allen, J., Jacobs, S. A., & Essen, B. C. V. (2019) · arXiv (Cornell University) · doi:10.48550/arxiv.1901.11152 · Cited by 1

Modeling the Heterogeneous Brain Tumor Microenvironment to Analyze Mechanisms of Vascular Development and Chemoresistance

Cox, M. C. (2018) · VTechWorks (Virginia Tech) · Cited by 1

Constitutively active TrkB kinase signalling reduces actin filopodia dynamics and cell migrationPreprint

Gupta, R., Bauer, M., Wohlleben, G., Luzak, V., Wegat, V., Segebarth, D., Bady, E., Langlhofer, G., Wachter, B., Havlicek, S., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.11.292565 · Cited by 1

Robust Formation of Optimal Single Spheroids towards Cost-Effective In-Vitro 3-Dimensional Tumor ModelsPreprint

Habra, K., Pearson, J. R. D., & McArdle, S. (2022) · Research Square · doi:10.21203/rs.3.rs-1695738/v1 · Cited by 1

Novel Therapeutic Approaches to Induce Autophagy in Brain Cancer

Conway, G. E. (2016) · Arrow - TU Dublin (Technological University Dublin) · doi:10.21427/d7632v

Studies on microglia in tumor biology and neurobiology

Shen, X. (2017) · Figshare

Radioresistencia en glioblastoma: papel de la hipoxia en la genotoxicidad inducida por radiaciones ionizantes

Forero, K. C., Langer, M. B., Paternina, A. F. M., Vega, C. M., Calvete, P. C. R., Guerra, A. M., Cruz-Cuevas, J. D., Suta, J. C., Martínez, M. A., Herrera, D. P., et al. (2018) · Ciencia e Investigación Medico Estudiantil Latinoamericana · doi:10.23961/cimel.v23i1.1066

Engineering PNIPAAm Biomaterial Scaffolds to Model Microenvironmental Regulation of Glioblastoma Stem-Like Cells

Heffernan, J. M. (2017)

An Overview of Preclinical Mouse Models for Brain Tumors

Ozawa, T. (2018) · Japanese Journal of Neurosurgery · doi:10.7887/jcns.27.752

Estudo da administração de fitol e retinol sobre linhagens celulares humanas de glioblastoma

Facchini, G. (2018) · doi:10.47749/t/unicamp.2018.1061823

The Role of BCL6 in Glioblastoma

Jones, N. M. (2018) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.17072567

Animal models of primary brain tumors

Kolb, B. L., Fadel, H. A., Klinger, N. V., & Mittal, S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814704-7.00007-6

Cell-based models for studying paediatric high-grade gliomas

Larsson, S. C. (2019) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Investigating the role of the apelinergic system in glioblastoma

Venkatesh, V. S. (2018) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.17134046

COMP-05. A DRUG ASSOCIATION MAP OF GLIOBLASTOMA INFORMS PRECISION TARGETING OF p53-DEPENDENT METABOLIC STATES

Johansson, P., Almstedt, E., Doroszko, M., Kundu, S., Vinel, C., Lane, D. P., Nestor, M., Marino, S., Krona, C. C., & Nelander, S. (2019) · Neuro-Oncology · doi:10.1093/neuonc/noz175.248

Biological Evaluation of a Potential Anticancer Agent Methyl N -[5-(3′-Iodobenzoyl)-1 H -Benzimidazol-2-yl]Carbamate

Kortylewicz, Z. P., Coulter, D. W., & Baranowska‐Kortylewicz, J. (2019) · Cancer Biotherapy and Radiopharmaceuticals · doi:10.1089/cbr.2019.2988

Preparation, stability testing and in vitro antiproliferative determination of ester and amide derivatives of Temozolomide

Ingham, O. (2020) · CLOK (University of Central Lancashire)

Rodent Brain Tumor Models for Neuro-Oncology Research

Otani, Y., McCormack, R., & Kaur, B. (2021) · Molecular pathology library · doi:10.1007/978-3-030-69170-7_12

Endogenous Melatonin Concentration Along With the Expression of Mitochondrial Regulator Genes Is Elevated by the Serum Shock Process in the U87-MG Cell LinePreprint

Balkhi, S., Jazi, M. S., Samaei, N. M., & Farahmand, M. (2021) · Research Square · doi:10.21203/rs.3.rs-881036/v1

A Customisable Cell Line Model of Glioblastoma

Forsythe, D. (2021) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.16632625.v1

Why is Immunohistochemical Detection of Metastasized Breast Cancer Cells in the Immunocompetent Host Not Always Easy?

Shenoy, P. A. (2018) · Journal of Analytical Oncology · doi:10.30683/1927-7229.2018.07.04.2

ACSVL3 is a Novel Therapeutic Target in Glioblastoma: Drug Discovery and Role in Protein Lipidation

Clay, E. M. (2017)

“Endogenous Melatonin Concentration Along with the Expression of Mitochondrial Regulator Genes is Elevated by the Serum Shock Process in the U87-MG Cell Line”Preprint

Balkhi, S., Jazi, M. S., Samaei, N. M., & Farahmandrad, M. (2022) · Research Square · doi:10.21203/rs.3.rs-881036/v2

Die Rolle von Arlts1 im Glioblastoma multiforme

Ostmeier, K. (2020) · doi:10.53846/goediss-8041

Endogenous melatonin concentration along with the expression of mitochondrial regulator genes is elevated by the serum shock process in the U87-MG cell linePreprint

Balkhi, S., Jazi, M. S., Samaei, N. M., & Farahmandrad, M. (2022) · Research Square · doi:10.21203/rs.3.rs-881036/v3

Reporting of results

OECD (2018) · OECD series on testing and assessment · doi:10.1787/9789264304796-14-en

List of viability testing methods (non-inclusive) of cell cultures

OECD (2018) · OECD series on testing and assessment · doi:10.1787/9789264304796-24-en

Глиобластома и стволовые клетки костного мозга

Брюховецкий, И. С., Брюховецкий, А. С., Хотимченко, Ю. С., Пак, О. И., Zaitsev, S., Шевченко, В. Е., & Lyakhova, I. (2020) · Publishing House of Far Eastern Federal University eBooks · doi:10.24866/7444-4837-0

In Vitro Antiproliferative and Free Radical Scavenging Activities in Peels of Citrus Fruits

Pallavi, M., Ramesh, C. K., Krishna, V., & Parveen, S. (2018) · Research Journal of Life Sciences Bioinformatics Pharmaceutical and Chemical Sciences · doi:10.26479/2018.0404.26

การแสดงออกของยนและคณลกษณะของเซลลตนกำเนดมะเรงในประชากรเซลลไลน U87MG glioblastoma

บุตรศรี, ร. (2020) · doi:10.58837/chula.the.2020.685

Increasing the accuracy of glioblastoma subtypes: Factoring in the tumor's cell of origin

Nelander, S. (2017) · Molecular & Cellular Oncology · doi:10.1080/23723556.2017.1302907 · Cited by 1

Glioblastoma Cell Malignancy and Drug Sensitivity Are Affected by the Cell of Origin

Jiang, Y., Marinescu, V. D., Xie, Y., Jarvius, M., Maturi, N. P., Haglund, C., Olofsson, S. K., Lindberg, N., Olofsson, T., Leijonmarck, C., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.04.053 · Cited by 14

Establishment of attached and non‐attached cell lines from an uncommon human glioma

Westermark, B., Larsson, E., Brunk, U. T., Lubitz, W., & Mark, J. (1981) · International Journal of Cancer · doi:10.1002/ijc.2910280314 · Cited by 17

A study of the origin of human glioma based on cell lines and tumor specimens

Timin, G., Лахина, Ю. С., Gulyaev, D. A., & Tolkunova, E. N. (2016) · Cell and Tissue Biology · doi:10.1134/s1990519x16020103