TMOD-14. A PATIENT-DERIVED CANCER CELL LINE ATLAS OF PRIMARY AND METASTATIC CENTRAL NERVOUS SYSTEM TUMORS. (5th November 2018)
- Record Type:
- Journal Article
- Title:
- TMOD-14. A PATIENT-DERIVED CANCER CELL LINE ATLAS OF PRIMARY AND METASTATIC CENTRAL NERVOUS SYSTEM TUMORS. (5th November 2018)
- Main Title:
- TMOD-14. A PATIENT-DERIVED CANCER CELL LINE ATLAS OF PRIMARY AND METASTATIC CENTRAL NERVOUS SYSTEM TUMORS
- Authors:
- De Smet, Frederik
Tseng, Yuen-Yi
Ramkissoon, Shakti
Ramkissoon, Lori
Pelton, Kristine
Luna, Ruben Ferrer
Panovska, Dena
Schoolcraft, Kate
Watkinson, Fiona
Bilton, Shawna
Hung, Victoria
Chow, Kin-Hoe
Geduldig, Jack
Becker, Sarah
Jones, Robert
Keskula, Paula
Alkhairy, Sahar
Delmar, Mimoun
Arraya, Josh
Oh, Crystal
Yeagley, Alexa
Kramm, Anneke
Chiocca, E Antonio
Bi, Wenya (Linda)
Kieran, Mark
Alexander, Brian
Dunn, Ian
Beroukhim, Rameen
Boehm, Jesse
Ligon, Keith - Abstract:
- Abstract: BACKGROUND: Tumors involving the central nervous system (CNS) include over 200 primary and metastatic subtypes with major clinical impact. Research on CNS neoplasms has been hampered by the lack of appropriate models for many subtypes. We established a robust workflow and systematic culturing approach to create cancer cell line models from all adult and pediatric CNS cancer patients and here report the results of these ongoing efforts. METHODS: Tumor samples from consented patients with CNS cancers were systematically collected from 2008–18. Tumors were grown in different media and substrates and growth verified by >5 passages. Genomic verification was performed using NGS analysis (focused SNV and CNA) and expression profiling assays. RESULTS: We attempted to generate cell line models from >1500 consented brain tumor patients at the Brigham and Women's and Boston Children's Hospital (IRB-10–417) under the DFCI Living Tissue Bank Program as well as within the Broad Institute Cancer Cell Line Factory (CCLF) Project and the Leuven Living Tissue Bank (IRB-S59804, Belgium). 120 different tumor types, including high and low-grade brain tumors of both adult and pediatric origin, were evaluated for in vitro growth in >2000 culturing attempts. The success rate of growing high-grade tumors (i.e. glioma and of other origin) was robustly high (~50%), while the growth verification rate for low-grade tumors remained low (<1%). Overall, growth beyond passage 5 was achieved inAbstract: BACKGROUND: Tumors involving the central nervous system (CNS) include over 200 primary and metastatic subtypes with major clinical impact. Research on CNS neoplasms has been hampered by the lack of appropriate models for many subtypes. We established a robust workflow and systematic culturing approach to create cancer cell line models from all adult and pediatric CNS cancer patients and here report the results of these ongoing efforts. METHODS: Tumor samples from consented patients with CNS cancers were systematically collected from 2008–18. Tumors were grown in different media and substrates and growth verified by >5 passages. Genomic verification was performed using NGS analysis (focused SNV and CNA) and expression profiling assays. RESULTS: We attempted to generate cell line models from >1500 consented brain tumor patients at the Brigham and Women's and Boston Children's Hospital (IRB-10–417) under the DFCI Living Tissue Bank Program as well as within the Broad Institute Cancer Cell Line Factory (CCLF) Project and the Leuven Living Tissue Bank (IRB-S59804, Belgium). 120 different tumor types, including high and low-grade brain tumors of both adult and pediatric origin, were evaluated for in vitro growth in >2000 culturing attempts. The success rate of growing high-grade tumors (i.e. glioma and of other origin) was robustly high (~50%), while the growth verification rate for low-grade tumors remained low (<1%). Overall, growth beyond passage 5 was achieved in ~30% of cases, and of the growth verified models, also ~30% were genomically verified to represent cancer, with the majority maintaining genomic and/or transcriptional features. In addition to primary CNS tumors, we were now also able to grow metastatic cultures, resulting in >150 novel model systems covering >20 primary and metastatic diagnoses. CONCLUSION: Patient-derived cell lines may be created at scale from primary and metastatic CNS tumors to support pre-clinical cancer research but technological improvements will be required to culture even more tumor types. … (more)
- Is Part Of:
- Neuro-oncology. Volume 20(2018)Supplement 6
- Journal:
- Neuro-oncology
- Issue:
- Volume 20(2018)Supplement 6
- Issue Display:
- Volume 20, Issue 6 (2018)
- Year:
- 2018
- Volume:
- 20
- Issue:
- 6
- Issue Sort Value:
- 2018-0020-0006-0000
- Page Start:
- vi271
- Page End:
- vi271
- Publication Date:
- 2018-11-05
- Subjects:
- Brain Neoplasms -- Periodicals
Brain -- Tumors -- Periodicals
Brain -- Cancer -- Periodicals
Nervous system -- Cancer -- Periodicals
616.99481 - Journal URLs:
- http://neuro-oncology.dukejournals.org/ ↗
http://neuro-oncology.oxfordjournals.org/ ↗
http://www.oxfordjournals.org/content?genre=journal&issn=1522-8517 ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/neuonc/noy148.1126 ↗
- Languages:
- English
- ISSNs:
- 1522-8517
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.288000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12326.xml