Establishment and Biological Characterization of a Panel of Glioblastoma Multiforme (GBM) and GBM Variant Oncosphere Cell Lines

被引:19
|
作者
Binder, Zev A. [1 ,2 ,3 ,7 ]
Wilson, Kelli M. [1 ,8 ]
Salmasi, Vafi [1 ,9 ]
Orr, Brent A. [4 ,10 ]
Eberhart, Charles G. [4 ]
Siu, I-Mei [1 ]
Lim, Michael [1 ,5 ]
Weingart, Jon D. [1 ,5 ]
Quinones-Hinojosa, Alfredo [1 ,5 ]
Bettegowda, Chetan [1 ,5 ]
Kassam, Amin B. [6 ]
Olivi, Alessandro [1 ,5 ]
Brem, Henry [1 ,5 ]
Riggins, Gregory J. [1 ,5 ]
Gallia, Gary L. [1 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Johns Hopkins Phys Sci Oncol Ctr, Baltimore, MD USA
[3] Johns Hopkins Univ, Inst NanoBioTechnol, Baltimore, MD USA
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[6] Aurora Neurosci Innovat Inst, Dept Neurosurg, Milwaukee, WI USA
[7] Univ Penn, Dept Neurosurg, Philadelphia, PA 19104 USA
[8] NIH, Div Preclin Innovat, Chem Genom Ctr, Natl Ctr Adv Translat Sci, Rockville, MD USA
[9] Cleveland Clin, Inst Anesthesiol, Cleveland, OH 44106 USA
[10] St Jude Childrens Res Hosp, Dept Pathol, 332 N Lauderdale St, Memphis, TN 38105 USA
来源
PLOS ONE | 2016年 / 11卷 / 03期
基金
美国国家卫生研究院;
关键词
STEM-CELLS; CROSS-CONTAMINATION; TUMOR; RESISTANCE; PHENOTYPE; GENOTYPE; CULTURE; GROWTH;
D O I
10.1371/journal.pone.0150271
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective Human tumor cell lines form the basis of the majority of present day laboratory cancer research. These models are vital to studying the molecular biology of tumors and preclinical testing of new therapies. When compared to traditional adherent cell lines, suspension cell lines recapitulate the genetic profiles and histologic features of glioblastoma multiforme (GBM) with higher fidelity. Using a modified neural stem cell culture technique, here we report the characterization of GBM cell lines including GBM variants. Methods Tumor tissue samples were obtained intra-operatively and cultured in neural stem cell conditions containing growth factors. Tumor lines were characterized in vitro using differentiation assays followed by immunostaining for lineage-specific markers. In vivo tumor formation was assayed by orthotopic injection in nude mice. Genetic uniqueness was confirmed via short tandem repeat (STR) DNA profiling. Results Thirteen oncosphere lines derived from GBM and GBM variants, including a GBM with PNET features and a GBM with oligodendroglioma component, were established. All unique lines showed distinct genetic profiles by STR profiling. The lines assayed demonstrated a range of in vitro growth rates. Multipotency was confirmed using in vitro differentiation. Tumor formation demonstrated histologic features consistent with high grade gliomas, including invasion, necrosis, abnormal vascularization, and high mitotic rate. Xenografts derived from the GBM variants maintained histopathological features of the primary tumors. Conclusions We have generated and characterized GBM suspension lines derived from patients with GBMs and GBM variants. These oncosphere cell lines will expand the resources available for preclinical study.
引用
收藏
页数:18
相关论文
共 50 条
  • [41] Overexpression of MARCKS in EGFRvIII-expressing glioblastoma multiforme (GBM)
    Micallef, J
    Caldwell, J
    Moran, M
    Guha, A
    [J]. NEURO-ONCOLOGY, 2004, 6 (04) : 319 - 319
  • [42] Mechanisms of Resistance and Current Treatment Options for Glioblastoma Multiforme (GBM)
    Yalamarty, Satya Siva Kishan
    Filipczak, Nina
    Li, Xiang
    Subhan, Md Abdus
    Parveen, Farzana
    Ataide, Janaina Artem
    Rajmalani, Bharat Ashok
    Torchilin, Vladimir P.
    [J]. CANCERS, 2023, 15 (07)
  • [43] microRNAs (miRNAs) in Glioblastoma Multiforme (GBM)-Recent Literature Review
    Makowska, Marianna
    Smolarz, Beata
    Romanowicz, Hanna
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (04)
  • [44] Activation of Notch signaling contributes to human glioblastoma multiforme (GBM)
    Kanamori, M
    Nigro, J
    Feuerstein, B
    Haas-Kogan, D
    Stokoe, D
    Berger, MS
    Miele, L
    Pieper, RO
    [J]. NEURO-ONCOLOGY, 2004, 6 (04) : 317 - 317
  • [45] Impact of extent of resection of glioblastoma multiforme (GBM) in the era of chemoradiation
    Slotman, B. J.
    Eppinga, W. S.
    Reijneveld, J. C.
    Noske, D. P.
    Buter, J.
    Braam, L. M.
    Lagerwaard, F. J.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (15)
  • [46] MET and ALK in glioblastoma multiforme (GBM): Comparison of IHC and FISH
    Kulig, Kimary
    McLendon, Roger E.
    Locke, Susan C.
    Young, Debra R.
    Zhong, Xiaoyin
    Hudson, Lori L.
    Abernethy, Amy Pickar
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (15)
  • [47] Telomerase inhibition brings metabolic compromises in glioblastoma multiforme (GBM)
    Ahmad, Fahim
    Sen, Ellora
    [J]. CANCER RESEARCH, 2016, 76
  • [48] Toxicity of concurrent and adjuvant temozolomide in patients with glioblastoma multiforme (GBM).
    Mcmahon, David
    Hussein, Awab
    Mangleburg, Hunter
    Nichianain, Aine
    Fitzpatrick, Orla
    McLaughlin, Ronan Andrew
    Conroy, Michael R.
    Marks, Sam Jonathan
    Naidoo, Jarushka
    Grogan, William
    Murphy, Adrian Gerard
    Breathnach, Oscar S.
    Hennessy, Bryan T.
    Morris, Patrick G.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2022, 40 (16)
  • [49] Long-term survival of patients with glioblastoma multiforme (GBM)
    Smoll, Nicolas R.
    Schaller, Karl
    Gautschi, Oliver P.
    [J]. JOURNAL OF CLINICAL NEUROSCIENCE, 2013, 20 (05) : 670 - 675
  • [50] Radiotherapy-related Tiredness in Patients with Glioblastoma Multiforme (GBM)
    Tuna-Malak, Arzu
    Diramali, Alev
    [J]. ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2008, 9 (03) : 497 - 499