New Insights into NB Heterogeneity and NB-Associated Microenvironment

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cell Microenvironment".

Deadline for manuscript submissions: closed (30 September 2021) | Viewed by 2816

Special Issue Editors


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Guest Editor
Department of Experimental Medicine (DIMES), University of Genova, 16132 Genova, Italy
Interests: cytokines; natural killer cells; tumor microenvironment; myeloid cells
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Guest Editor
Department of Experimental Medicine, University of Genova, 16132 Genova, Italy
Interests: NK; TGF(2); IL; neuroblastoma; tumor immunology

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Guest Editor
Pediatric Oncology Unit, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy
Interests: NK; TGF(2); IL; neuroblastoma; tumor immunology

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Guest Editor
Fondazione Instituto di Ricerca Pediatrica Citta’ della Speranza, Neuroblastoma Laboratory, 35127 Padua, Italy
Interests: NK; TGF(2); IL; neuroblastoma; tumor immunology

Special Issue Information

Dear Colleagues,

Neuroblastoma (NB) is the most frequent extracranial solid tumor of childhood, causing 10% of deaths in cancer patients. Its origin from embryonic neural cell crests is responsible for the high NB heterogeneity in terms of both histological and clinical features. Characterized by a primary mass commonly arising in the adrenal medulla or sympathetic ganglia, NB clinical variants range from spontaneously regressing to metastatic high-risk diseases with a dismal prognosis despite the combined therapies used. These therapies include aggressive chemotherapy and autologous stem cell transplantation, followed by the infusion of antibodies targeting the disialoganglioside GD2. Unfortunately, patients may show resistance to chemotherapy or, after a complete or partial remission at the end of the standard therapeutic protocol, fatal progressions, often due to relapses associated with bone marrow (BM) metastases. Moreover, a subset of NB lacking GD2 has been recently described unveiling a novel mechanism of NB resistance and suggesting the need for alternative immunotherapeutic approaches.

With these premises, new personalized therapeutic chances for patients might derive from the integrated genetic, biological, and immunophenotypic analysis of NB, both at primary and metastatic sites, to define new mechanisms of NB resistance and discover innovative therapeutic targets. The new knowledge will be useful also to optimize diagnosis, risk stratification, and prognosis.

We should also consider that, due to the low number of recurrent NB driver mutations, additional important data might derive from the study of the NB microenvironment, including the characterization of the immune effectors involved in NB recognition and killing.

Therefore, the present Special Issue aims to open new discussions on:

  • Genetic, biological, immune-phenotypic, and functional properties of NB cells;
  • Phenotypic and functional properties of cells composing the NB microenvironment;
  • Mechanisms influencing NB aggressiveness and response to therapies;
  • Novel therapeutic/immunotherapeutic approaches, including adoptive cell-based strategies;
  • Efficacy of computational strategies for finding new therapeutic targets.

Original articles or other article types including reviews, mini-reviews, and commentaries are welcome.

Dr. Roberta Castriconi
Dr. Alessandra Dondero
Dr. Alberto Garaventa
Dr. Sanja Aveic
Guest Editors

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Keywords

  • NB biology
  • NB-immumophenotype
  • immune landscape
  • NB microenvironment

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Published Papers (1 paper)

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13 pages, 1680 KiB  
Case Report
Integrated CGH/WES Analyses Advance Understanding of Aggressive Neuroblastoma Evolution: A Case Study
by Diana Corallo, Carlo Zanon, Marcella Pantile, Gian Paolo Tonini, Angelica Zin, Samuela Francescato, Bartolomeo Rossi, Eva Trevisson, Claudia Pinato, Ezequiel Monferrer, Rosa Noguera, Salvador F. Aliño, Maria Jose Herrero, Alessandra Biffi, Elisabetta Viscardi and Sanja Aveic
Cells 2021, 10(10), 2695; https://doi.org/10.3390/cells10102695 - 9 Oct 2021
Cited by 3 | Viewed by 2277
Abstract
Neuroblastoma (NB) is the most common extra-cranial malignancy in preschool children. To portray the genetic landscape of an overly aggressive NB leading to a rapid clinical progression of the disease, tumor DNA collected pre- and post-treatment has been analyzed. Array comparative genomic hybridization [...] Read more.
Neuroblastoma (NB) is the most common extra-cranial malignancy in preschool children. To portray the genetic landscape of an overly aggressive NB leading to a rapid clinical progression of the disease, tumor DNA collected pre- and post-treatment has been analyzed. Array comparative genomic hybridization (aCGH), whole-exome sequencing (WES), and pharmacogenetics approaches, respectively, have identified relevant copy number alterations (CNAs), single nucleotide variants (SNVs), and polymorphisms (SNPs) that were then combined into an integrated analysis. Spontaneously formed 3D tumoroids obtained from the recurrent mass have also been characterized. The results prove the power of combining CNAs, SNVs, and SNPs analyses to assess clonal evolution during the disease progression by evidencing multiple clones at disease onset and dynamic genomic alterations during therapy administration. The proposed molecular and cytogenetic integrated analysis empowers the disease follow-up and the prediction of tumor recurrence. Full article
(This article belongs to the Special Issue New Insights into NB Heterogeneity and NB-Associated Microenvironment)
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