Neuroblastoma treatment in the post-genomic era. Issue 1 (December 2017)
- Record Type:
- Journal Article
- Title:
- Neuroblastoma treatment in the post-genomic era. Issue 1 (December 2017)
- Main Title:
- Neuroblastoma treatment in the post-genomic era
- Authors:
- Esposito, Maria
Aveic, Sanja
Seydel, Anke
Tonini, Gian - Abstract:
- Abstract Neuroblastoma is an embryonic malignancy of early childhood originating from neural crest cells and showing heterogeneous biological, morphological, genetic and clinical characteristics. The correct stratification of neuroblastoma patients within risk groups (low, intermediate, high and ultra-high) is critical for the adequate treatment of the patients. High-throughput technologies in the Omics disciplines are leading to significant insights into the molecular pathogenesis of neuroblastoma. Nonetheless, further study of Omics data is necessary to better characterise neuroblastoma tumour biology. In the present review, we report an update of compounds that are used in preclinical tests and/or in Phase I-II trials for neuroblastoma. Furthermore, we recapitulate a number of compounds targeting proteins associated to neuroblastoma: MYCN (direct and indirect inhibitors) and downstream targets, Trk, ALK and its downstream signalling pathways. In particular, for the latter, given the frequency ofALK gene deregulation in neuroblastoma patients, we discuss on second-generation ALK inhibitors in preclinical or clinical phases developed for the treatment of neuroblastoma patients resistant to crizotinib. We summarise how Omics drive clinical trials for neuroblastoma treatment and how much the research of biological targets is useful for personalised medicine. Finally, we give an overview of the most recent druggable targets selected by Omics investigation and discuss how theAbstract Neuroblastoma is an embryonic malignancy of early childhood originating from neural crest cells and showing heterogeneous biological, morphological, genetic and clinical characteristics. The correct stratification of neuroblastoma patients within risk groups (low, intermediate, high and ultra-high) is critical for the adequate treatment of the patients. High-throughput technologies in the Omics disciplines are leading to significant insights into the molecular pathogenesis of neuroblastoma. Nonetheless, further study of Omics data is necessary to better characterise neuroblastoma tumour biology. In the present review, we report an update of compounds that are used in preclinical tests and/or in Phase I-II trials for neuroblastoma. Furthermore, we recapitulate a number of compounds targeting proteins associated to neuroblastoma: MYCN (direct and indirect inhibitors) and downstream targets, Trk, ALK and its downstream signalling pathways. In particular, for the latter, given the frequency ofALK gene deregulation in neuroblastoma patients, we discuss on second-generation ALK inhibitors in preclinical or clinical phases developed for the treatment of neuroblastoma patients resistant to crizotinib. We summarise how Omics drive clinical trials for neuroblastoma treatment and how much the research of biological targets is useful for personalised medicine. Finally, we give an overview of the most recent druggable targets selected by Omics investigation and discuss how the Omics results can provide us additional advantages for overcoming tumour drug resistance. … (more)
- Is Part Of:
- Journal of biomedical science. Volume 24:Issue 1(2017)
- Journal:
- Journal of biomedical science
- Issue:
- Volume 24:Issue 1(2017)
- Issue Display:
- Volume 24, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 24
- Issue:
- 1
- Issue Sort Value:
- 2017-0024-0001-0000
- Page Start:
- 1
- Page End:
- 16
- Publication Date:
- 2017-12
- Subjects:
- Neuroblastoma -- Omics -- Personalised medicine -- Targeted therapy
Medical sciences -- Periodicals
610.28 - Journal URLs:
- http://www.jbiomedsci.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=857&action=archive ↗
http://www.springer.com/gb/ ↗
http://firstsearch.oclc.org ↗
http://www.springerlink.com/content/112912/ ↗ - DOI:
- 10.1186/s12929-017-0319-y ↗
- Languages:
- English
- ISSNs:
- 1021-7770
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4953.769000
British Library DSC - BLDSS-3PM
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- 10053.xml